User:CopperKettle - Wikipedia
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I live in Ekaterinburg, Russia. As of 2019, I'm a freelance translator specializing in biochem, biotech and pharma. My interests include psychiatry and neuroscience. And history of Russia.
I love the music of Bob Dylan, Boris Grebenshikov (Aquarium), Frank Zappa, Chumbawamba, Umka and Beethoven's string quartets. I enjoy skiing and jogging, playing tennis.
My favourite authors are Solzhenitsyn, Updike, Pelevin, Dostoyevsky, Vonnegut.
I participate in the Folding@home project. My last.fm account is here.
My Wikimedia page.
P.S. Reelin' cookies: If you know a foreign language into which Reelin is not yet translated, start a stub - and I will give you a cookie.
Pages I've started (about 149 thus far)
In no particular order, but generally newest up:
- Mild non-BH4-deficient hyperphenylalaninemia
- Jennifer Reeser - poet
- Riboflavine-responsive exercise intolerance
- Tyrosine hydroxylase deficiency
- Autosomal dominant GTP cyclohydrolase I deficiency
- Autosomal recessive GTP cyclohydrolase I deficiency
- Protocadherin 19
- Pterin-4 alpha-carbinolamine dehydratase deficiency
- SET domain containing protein 1A (schizophrenia, autism, etc.)
- Methylenetetrahydrofolate dehydrogenase 1 deficiency
- Transcorneal electrical stimulation
- Branched-chain keto acid dehydrogenase kinase deficiency
- DDX3X syndrome
- Mitochondrial folate transporter
- Dihydrofolate reductase deficiency
- Dihydropteridine reductase deficiency
- 5,10-methenyltetrahydrofolate synthetase deficiency
- Baranchinsky settlement
- Robert L. Leahy, cognitive behaviour therapy
- Cerebral folate deficiency - was a redirect, I strove to revive it
- Lobva settlement in Sverdlovsk Oblast
- Pervouralsk New Pipe Plant
- Marlene Laruelle
- Gordon M. Hahn
- Zayd Saidov
- Maksud Ibragimov
- Group 24 - 29 April 2015
- Reftinskaya GRES
- Mohr-Tranebjaerg syndrome
- Anti-NMDA receptor encephalitis
- Inhibitory Control Test
- ABCA13
- Isaakievsky Bridge
- Pelageya
- Old man Bukashkin
- Adult-onset basal ganglia disease
- Hudson-Stahli line
- Last bell
- Scrambler mouse
- Pyridoxine-dependent epilepsy
- Collapsin response mediator protein family
- Noopept
- Megalocornea
- Cornea plana 1
- Cornea plana 2
- Sclerocornea
- Epithelial basement membrane dystrophy
- Gelatinous drop-like corneal dystrophy
- Subepithelial mucinous corneal dystrophy
- Lisch epithelial corneal dystrophy
- Granular corneal dystrophy type II
- Granular corneal dystrophy type I
- Lattice corneal dystrophy type I
- Fleck corneal dystrophy
- Schnyder crystalline corneal dystrophy
- Pyotr Gannushkin
- Posterior amorphous corneal dystrophy
- Congenital stromal corneal dystrophy
- Congenital endothelial dystrophy type 1
- Congenital endothelial dystrophy type 2
- Posterior polymorphous corneal dystrophy 3
- Posterior polymorphous corneal dystrophy 2
- X-linked endothelial corneal dystrophy
- Corneal dystrophy of Bowman layer, type II
- Reis-Bucklers corneal dystrophy
- J. Wayne Streilein (eye immune system)
- Corneal keratocyte - distinct from fish epidermal keratocyte
- Pancreatic stellate cell
- Macular corneal dystrophy
- posterior polymorphous corneal dystrophy
- KC6 gene (a stub)
- ZNF804A
- Erminio Costa
- Nitrotyrosine
- Ramon Castroviejo - corneal transplantation pioneer
- TBR1
- Ribbon synapse
- Pantogam
- Manifesto of three-day corvee
- Vyngapur River
- Paris, a village with its own Eiffel Tower.
- Oak of Mamre - a copy from Orthodox Wiki
- Abraham's Oak Holy Trinity Monastery
- Fershampenuaz
- Paul R. McHugh
- DAB1
- Cajal-Retzius cell
- Reeler
- VLDL receptor
- Yotari
- Pioneer neuron
- Low density lipoprotein receptor gene family
- Radial glia
- Martinotti cell
- Homovanillic acid
- Victor Pavlovich Protopopov
- Subventricular zone
- Subplate zone (brain)
- Umka and the armoured car
- Chandelier neuron - did a little stub, will try to expand.
- Vladimir Alekseyevich Betz - done.
- NPAS3 - resides in HAR21 region, linked to schizophrenia; knockout mice show decrease in reelin expression. Did a stub.
- ApoER2 - stub.
- Shaking rat Kawasaki
- Cystatin C - stub.
- Subgranular zone - stub.
- Alpha-enolase
- Neuregulin 1
- GAB2 - stub based on a BBC news report.
- Leukoencephalopathy with vanishing white matter - stub based on this comment.
- Douglas Scott Falconer - tiny stub.
- D-amino acid oxidase activator
- RGS4 - stub.
- DISC1 - stub.
- Chakragati mouse - a hasty stub.
- NARSAD - stub.
- GPR35 receptor; stub
- S100B - brain-specific protein; potential neurophathology marker. PMID 17348038.
- myeloid/lymphoid or mixed-lineage leukemia 1, Mixed Lineage Leukemia 1 or MLL1, Mll1; may be involved in GAD1 downreg. in schiz. (OMIM?) gene db at pubmed
- biogenesis of lysosome-related organelles complex 1, or BLOC-1, which includes dysbindin.
- Kalirin (OMIM 604605), including its isoform Kalirin-7; based on a text from schizophreniaforum.org.
- Norman-Roberts syndrome, a rare lissencephaly syndrome caused by a mutation in the reelin gene.
- VLDLR-associated cerebellar hypoplasia
- Huntingtin-associated protein 1
- VGF protein - increased expression in schizophrenia (CSF samples). (OMIM)
- CABP1 or Caldendrin, a novel Calcium-binding protein.
- Yuri Nuller, Yuri Lvovich Nuller, Russian psychiatrist.
- GHB receptor - apparently bound by sulpiride and amisulpride.
- Frank Ayd, american psychiatrist
- Kenyon cell - neurons in insects; little stub
- Ganglionic eminence
- Pikachurin, a real kewl protein.
- Andrei Snezhnevsky, notorious Soviet psychiatrist.
- List of people on stamps of Mauritius - never knew I would start that...
- Copper Kettle - ..but this one was rather predictable
- So Soon In The Morning, a beautiful song, especially in Baez' rendition of 1959
- Brahin, a small settlement in Belarus where my ancestors lived.
- Bibishki
- Pyrotherapy
- Molebka
- Braginka river
- Willem-Karel Dicke
- Border cell (brain)
- Myoclonic dystonia
- Bullous keratopathy
- Reticulons
- Taganay
- Zyuratkul' National Park
- (temp);
- As a standalone: ?Dysarthria-clumsy hand syndrome due to mini-stroke; discovered by C. Miller Fisher in 1969
- ?Covert brain infarction - very interesting
- ??Episodic future thinking, if this is a robust concept. Came across it in a paper about anorexia nervosa.
- Auditory Continuous Performance Test (ACPT) - ""effectively differentiates healthy people from those with psychosis" (2024)
- ?Protein lactylation - for instance, of SNAP91, which happens due to exercise and confers resilience to stress
- Childhood-onset striatonigral degeneration discovered in 2016
- Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome - FLVCR2 gene; also known as Fowler syndrome, not to be confused with Fowler's syndrome
- Cystathionine beta-synthase deficiency as a standalone?
- Chromosome 9p deletion syndrome - OMIM 158170
- Levoleucovorin as a standalone - a formulation mentioned by Richard Frye in his update in 2024; efficacy not studied yet
- Non-ketotic hyperglycemic hemichorea (NHH), also known as diabetic striatopathy or chorea, hyperglycemia, basal ganglia (C-H-BG) syndrome
- ?Central retinal vein equivalent - elevated in keratoconus
- ?Cerebrovascular reactivity
- ?Central retinal arteriolar equivalent
- Changes in keratoconus; marker associated w/ arterial stiffness
- Mitochondrial complex III deficiency
- Bottom-of-Sulcus Dysplasia, cause of focal epilepsy
- ?John Maltsberger, psychoanalyst, investigated suicide
- ?Onconeural antibodies sometimes present with psychiatric symptoms
- ?Translocator protein distribution volume (TSPO VT) - an index of gliosis
- Global cortical atrophy scale, Pasquier scale, GCA scale
- ??Salpêtrière Retardation Rating Scale
- Intellectual developmental disorder-5
- SYNGAP1 gene
- CC-BY review, 2018, PMID 29402231
- What's the role of L-arginine?
- Review - CC-BY
- Fasting-mimicking diet
- ?Hypokalemic nephropathy curious
- eClinicalMedicine
- Glycerol intoxication as a standalone;
- Cochrane Database of Systematic Reviews as standalone;
- Rather high impact factor
- CHASERR - a lncRNA gene
- ?Anticholinergic burden as a standalone?
- 21-year study in SZ
- ?Progressive encephalomyelitis with rigidity and myoclonus, PERM
- As a standalone
- ??Aldosterone breakthrough on ACE inhibitor therapy
- Lean Mass Hyper-Responder, LMHR
- ??ddAVP challenge to investigate ACTH response, for instance
- Increased response associated w/resistant depression
- ?Edinburgh Postnatal Depression Scale
- Translate to Russian
- ?Transdiagnostic Sleep and Circadian Rhythm Intervention, or TranS-C - reportedly reduces depression (study in 2024);
- ??Respiratory muscle training, inspiratory muscle training
- ??Si-based agent, Silicon-based agent
- ?Methionine synthase reductase deficiency - psychiatric symptmos
- "CblE type"
- ?Holotranscobalamin, also HoloTC, presumably a good marker of B12 status
- used in phrases like HoloTC assay
- ??Sensory neuronopathy
- ?Daniel Javitt - glutamatergic dysfunction in SZ
- Glycine encephalopathy with normal serum glycine (OMIM 617301).
- ??Mind blanking in ADHD for instance
- ??Focal dyscognitive seizures
- ?Treatment-resistant schizophrenia
- MiR-1246 - could be associated with SZ
- Zelatriazin - investigational agonist of GPR139
- Total antioxidant capacity
- Cohen-Mansfield Agitation Inventory
- ?Nonketotic hyperglycemia-related epileptic seizures
- Also known as Non-ketotic hyperglycaemic seizures
- ?Aperiodic activity - EEG activity associated with ECT efficacy etc.
- ?Hypomyelinating disease as opposed to Demyelinating disease
- Or Hypomyelinating leukodystrophies - see a 2020 review
- SLC30A9 - variations traced back allegedly to Denisovans; mental illness
- ??DOCKopathies - DOCK9 is associated w/keratoconus 7
- ?Dystroglycanopathies
- ??Multicystic encephalomalacia - present in Russian as Мультикистозная энцефаломаляция
- ??? Typhoid psychosis
- ?? Chemiluminescent Microparticle Immunoassay (CMIA)
- ?Kristy Red-Horse of the North American Vascular Biology Organization
- ??Natural autoantibodies - O.o Could be low in some cases of autism
- ??Cystic Neutrophilic Granulomatous Mastitis
- ??13q32 - related genes? KC, SZ
- LNPK gene - developmental disorder, seizures (2018)
- ?Cooking fuel, to cover effects on development?
- PMID: 37419197 DOI: 10.1016/j.envres.2023.116528
- ?Ages and Stages Questionnaire to assess early development
- From ru:Куликов, Леонид Иванович
- ??Human restricted genes
- - related to Orphan gene?
- ??Subcallosal cingulate predicts effects of DBS in treatment resistant depression
- Human Psychopharmacology: Clinical and Experimental published since 1986, IF 2
- ??Massively parallel reporter assay (MPRA)
- Resolvin D1 may treat depression
- See Resolvin
- They include Mabry syndrome; their number is estimated at 19 or 21
- ??Random dot matrix tasks - for example, in OCD
- ?NRXN1 deletion syndrome
- ?? Hot sause paradigm
- Fecal lactoferrin for distinguishing between IBD and IBS
- ?? Antibody-mediated psychosis, Autoimmune psychosis
- Short-chain-enoyl-CoA hydratase - ECHS1
- ? Central vitamin B12 deficiency caused by antibodies to CD320, first announced in 2023
- ?? Emotional reactivity
- Augmented Depression Therapy (ADepT)
- Пиріг і Батіг - гарний фолк-гурт, з мови
- ? Zagociguat - investigational drug for MELAS, cognition in SZ
- ?? Standalone for Intranasal insulin? Effects on epilepsy, on cognition, in Alz, etc.
- ?? Standalone for Praxis-induced reflex seizures?
- ?? Standalone for Eating epilepsy, a form of reflex epilepsy?
- ? Standalone for Sunflower syndrome?
- ? Standalone for Nonconvulsive status epilepticus?
- Reviewed in PMID 28144933
- Amazing case in PMID 8683509 (misdiagnosed as psychiatric for 10 years, then cured)
- ?Non-motor seizures, such as Sensory seizures and Somatosensory seizures
- ?Medium-chain triglyceride ketogenic diet, MCT ketogenic diet
- -- as a standalone from Ketogenic diet
- ?James Davies (author) - "Cracked: Why Psychiatry is Doing More Harm than Good"
- ?Snaith-Hamilton-Pleasure-Scale, SHAPS
- ??? Mitohormesis > as a standalone
- ??Anti-basal ganglia autoantibodies, Anti-basal ganglia antibodies
- ??Basal ganglia encephalitis
- ?Exogenous insulin antibody syndrome (A 2018 review)
- Or as part of Insulin autoimmune syndrome (exists)?
- ??Hypoglycorrhachia
- ?Cyclic Cushing’s syndrome - extra-rare?
- ?Inspiratory muscle training, IMT, or Inspiratory muscle strength training, IMST
- "In a group of healthy adults, those who practiced high-resistance IMST for 30 breaths a day for six weeks saw their systolic blood pressure—the first number in a reading—drop by 9 millimeters of mercury"
- ??Adrenal hypertrophy in rodents, measured to assess stress in animal studies.
- ?Three bags task - measures maternal supportiveness
- Count Down (Shanna Swan book) - endocrine disruptors & sperm count
- Spastic paraplegia 56 - gene: CYP2U1
- Folate supplementation prevents cognitive decline in mouse model (curious)
- Signs of putative folate deficiency in patients (see OMIM)
- Early-onset vitamin B6-dependent epilepsy - responds to folinic acid
- ??Body sway assessed in PTSD
- ?Charlton Mabry - discoverer of Mabry syndrome (1968)
- ?Faciobrachial dystonic seizures - LGI1 encephalitis, religiosity, psychosis
- ??MDI-26478 - prototype drug for SZ
- ?A3243G - commonest mtDNA mutation
- Coffin-Siris syndrome 6 - gene assoc. with mosaic mutations in Bipolar
- ?Viktoria Lloyd-Barlow, author of 'All The Little Bird-Hearts'
- Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation or LBSL
- Into standalone: FAAH-OUT - lncRNA gene; pain insensitivity
- ?Nenad Blau - metabolism research (BH4, etc)
- ?Fecal elastase-1 test of exocrine pancreatic insufficiency
- and Coefficient of fat absorption (72 h fecal collection)
- ?Howard Pearson (1929-2016), Pearson syndrome
- ??Gluten ataxia as a standalone?
- Pete Walker (psychotherapist), author of Complex PTSD
- ?Tonic Immobility Scale to measure PTSD
- John Vervaeke
- Psychologist, author of books, Uni of Toronto
- ??Comb sign in Crohn's disease due to engorgement of Vasa recta (intestines)
- The Unfortunate Miss Bailey (song)
- Nikolay Zorya, Soviet prosecutor at Nuremberg trials
- Lissencephaly 10
- In some: "psychiatric abnormalities, including depression, bipolar disorder, hallucinations, aggressive behavior, and suicide attempts" (see OMIM)
- Might be assoc w/depression
- (2021)(REVIEW)(CC-BY) Iron, neuro-bioavailability and depression in eJHaem (IF: 4)
- Test of Detection of Cognitive Impairment in Alcoholism, TEDCA
- Dextran sulfate sodium to induce colitis
- Autosomal dominant intellectual developmental disorder 51
- OMIM 617788
- linked to autism
- ?Causes of treatment-resistant epilepsy
- ?Shankopathy or SHANKopathy (psychiatric disorders)
- Corrected with folinic acid: case report 2022
- "miR483-5p/Pgap2 pathway regulates anxiety"
- miR-483-5p plays a role in stress reduction
- Serial dependence (psychology) is a phenomenon that biases the perception of features or objects systematically toward sensory input from the recent past (Fischer & Whitney, 2014).
- Neurodevelopmental disorder with speech impairment and with or without seizures, NEDSIS
- OMIM 620144, gene: CACNAC1I
- This gene is assoc with both SZ and OCD
- ?Stages of Objective Memory Impairment (SOMI) for dementia prediction in the elderly
- ?Hyperorality
- "common in early stage bvFTD, arising prior to cognitive and neuroanatomic changes" (Christopher Morrow et al., 2022)
- Birk-Landau-Perez syndrome OMIM 617595
- SLC30A9 gene
- MEPAN syndrome - OMIM 617282
- Ameliorated by lipoic acid, presumably
- ?Prednisolone suppression test in depression
- "prednisolone should provide a more valid test of the HPA axis in depression" (Juruena et al 2018)
- Discovered galanin
- as a standalone
- As a separate page?
- mir-184, assoc w/keratoconus
- Assoc w/keratoconus
- ?5-Oxoprolinemia transient
- In Glutathione defiency (transient, for instance, with acetaminophen)
- Detection of Riboflavin deficiency
- redox/inflammation
- ?Minipuberty
- Riboflavin-responsive diseases -
- Into a separate article. Riboflavin as treatment
- FGF3 gene
- ?SLC25-associated diseases (List)
- EARS2 gene, mitochondrial enzyme
- Defects found in 2 patients with CFD
- Blunted in schizophrenia, linked to arachidonic acid pathway
- ?Antidepressant-induced hyponatremia
- ?ARA 290 peptide - Cibinetide
- ?PEPITEM peptide
- Obesity, inflammation
- A form of Ohtahara syndrome?
- 16p11.2 duplication syndrome (schizophrenia, autism)
- OMIM 614671
- OMIM 614688
- Huntingtin gene hypofunction
- Write more
- Autistic features
- rare but curious
- ?chronic unpredictable stress paradigm for depression studies
- ?Preclinical Alzheimer Cognitive Composite
- ZMYM4 gene
- Could be assoc w/schizophrenia via rs72657988
- ?Drinking in the dark - mouse model of binge drinking
- ?Maternal immune activation
- ??Primary antibody deficiencies
- Assoc w/psych disorders in offsprings
- any link to folate metabolism?
- Decreased in SZ, Bipolar
- Gene CHD8
- Investigated in ALZ's Disease, Parkinson's
- TIAM1 gene
- ?Sociovirology, in measles - causing encephalitis
- ?MAP4343, investigative antidepressant
- Pregnenolone derivative; might be used in alcoholism
- Sinking skin flap syndrome
- SORCS3 - ADHD, other psych disorders
- Collapsin response mediator protein 2 - ass w/psychosis
- Lasosamide - induced psychosis case
- CRMP2 and betaine? O_O
- ?Maximal electroshock seizure (MES) test of antiepileptic drugs
- Immunodeficiency, developmental delay, and hypohomocysteinemia
- OMIM 617744
- Gene - NRF2, related to keratoconus
- 2022 Review of numerous genes/causes: PMID 35328062 (CC-BY 4.0)
- ? Primary Neurotransmitter disorders
- Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
- Gene: TYROBP
- Putative neuroprotection in Parkinson's; counters inflammatory cytokine signaling
- AMED syndrome - gene - ADH5
- Lawrence F. Eng (-2004) - neuroscientist, discovered Glial fibrillary acidic protein
- Developmental delay with or without intellectual impairment or behavioral abnormalities
- OMIM 619575
- gene - TAOK1
- Prompted by a report on a psych forum of depression/halluc. of a guy on cyprofloxacine
- Example review (2020) in PubMed
- Neurodegeneration with brain iron accumulation 5 as standalone
- Gene: WDR45
- On withdrawal of dopamine medication
- CC-BY 2022 review in Cureus
- Gene: KDM6B, could be associated with CFD
- Mutations in CDC42 which affects dendritic spines
- Linked to Early-onset vitamin B6-dependent epilepsy (OMIM 617290)
- Is it worth reading? (example article)
- Pyridoxamine 5'-phosphate oxidase deficiency - PNPO gene mutations;
- Mega cisterna magna
- convert to standalone?
- Emraclidine, prototype
- Muscarinic, for schizophrenia
- Includes malondialdehyde, elevated in keratoconus serum
- First to attempt DBS in Parkinson's
- Autism and other manifestations; one of the genes: CYFIP1
- Two OMIM numbers: 613444 and 611913
- nongoitrous congenital hypothyroidism 6
- ?Bowman layer transplantation in keratoconus
- To standalone: KIF1A-associated neurological disorder
- ??Menstrual psychosis
- Alicia Juarrero - complexity, emergence, chaos theory, mind
- ??Pseudo-methylenetetrahydrofolate syndrome in excessive folic acid consumption
- 3-sulfogalactosyl diacylglycerols - anti-inflammatory; decrease in brain in aging
- AXA1125 - investigational for Chronic Fatigue Syndrome
- Charles Kenny (author)
- of the book "Plague Cycle"
- NMRAL1 gene, linked to SZ
- ?Scleromalacia perforans in Rh. arthritis
- SLC46A2
- Possible target of methotrexate in psoriasis
- ??standalone PTEN hamartoma tumor syndrome
- ??Fox eye shield
- ?Functional cognitive disorder
- ?Myoedema with mounding of muscle in hypothyroidism
- ?Infant head lag
- Intellectual developmental disorder, autosomal dominant 53
- Mutations in CAMKIIα
- Josep Dalmau, the discoverer of anti-NMDAR encephalitis
- ZSWIM8 - mutations affect the dab1/reelin pathway
- FOXG1 syndrome, see the FOXG1 gene
- Autism spectrum
- Antoine Lembert, Parisian surgeon, inventor of eponymous suture technique in 1826
- ??Secretin stimulation test of pancreatic exocrine function
- Hippocampal Splitter cell, also trajectory-dependent cell
- Bachmann-Bupp syndrome
- and ODC1 disorder - distinct?
- ??Polly Murray, patients' advocate, prompted the discovery of Lyme disease
- The Widening Circle, her book of 1996
- Emraclidine, investigational drug for schizophrenia
- Hermann Doose
- see myoclonic astatic epilepsy, aka Doose syndrome
- the RAC3 gene
- Gene: MRE11A
- protein that might be useful in diabetes
- PXDNL - possible association with reaction to antidepressants
- ??Congenital NAD deficiency disorder
- Might be too early to start it; see OMIM 617660 and 617661
- ?Hypoketotic hypoglycemia
- For instance, in deficiency of the mitochondrial folate transporter
- ?Standalone for Quincke's sign - nailbed pulsation in aortic regurgitation
- ??Electrical status epilepticus in sleep
- Small-bowel diaphragm disease or NSAID-induced small bowel stricture
- NSAID-induced
- gene: ATP2B1
- ??Prostaglandin-Associated Periorbital Syndrome
- ??Maternal autoantibody-related autism spectrum disorder
- Kleefstra syndrome-2, the gene is KMT2C
- Mutations in the gene might be associated with BH4 deficiency in refractory depression, per Lisa Pan et al., 2020
- Variants found in patients with refractory depression and BH4 deficiency by Lisa Pan et al., PMID 32128872
- The same snp rs79258645 as in Lisa Pan et al is associated w/keratoconus Layal Fadi Abi Farraj, 2015
- Mutations in NR4A2
- ??Phe loading test, Phenylalanine loading test (per guideline
- ??Treatabolome, treatable metabolic derangements
- ?Functional cognitive disorder
- ?Masaya Segawa, see Segawa syndrome
- International Parkinson and Movement Disorder Society
- Exists in German Wikipedia
- To distinguish Cushing's from Pseudo-Cushing's
- ?15q13.3 microduplication syndrome (detected by Lisa Pan in a person with resistant depression)
- ??Glycine receptor antibodies, anti-glycine receptor related disease, GlyR antibody encephalitis
- ??the same as Progressive encephalomyelitis with rigidity and myoclonus?
- ??Tryptophan catabolite pathway, TRYCAT pathway, involved in schizophrenia
- ?Simulated keratometry - see Keratometer
- ??Cold-restraint stress, animal model of gastric ulcers
- SETD1A - assoc. w/ autism and schizophrenia; disorder discovered in 2021
- Spastic tetraplegia, thin corpus callosum, and progressive microcephaly
- Deficient serine transport into the brain
- Methylenetetrahydrofolate dehydrogenase 1 deficiency or Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia (CIMAH)
- Blood–cerebrospinal fluid barrier as a standalone article
- Disfunction in cerebral folate deficiency
- Reviews: 2019 with mention of CFD
- Possible use in depression: review
- ?Folate trap in folate metabolism
- ?Oculomics - research of eye-based biomarkers of non-ophthalmological pathology
- Hypomyelinating leukodystrophy 6, also known as Hypomyelination with atrophy of basal ganglia and cerebellum
- Mutations in TUBB4A
- Might be associated with cerebral folate deficiency
- accompanied by cerebral folate deficiency? Folinic acid helps, per PMID 31340680 (review)
- Corneal endothelial dysfunction
- Cone-rod dystrophy 7
- Increased IQ, gene RIMS1
- ?m.8649_16084del, the second-most common mtDNA deletion in humans
- ?Theta burst stimulation for depression
- LAMM syndrome or Congenital deafness with labyrinthine aplasia, microtia, and microdontia
- OMIM 610706
- S-adenosylmethionine carrier, SLC25A26
- Intrinsic factor deficiency - OMIM 261000
- ??Peripheral nerve hyperexcitability
- Is it already described in Neuromyotonia etc?
- ?CASPR2-antibody encephalitis
- Part of Anti-VGKC-complex encephalitis? (a sloppy article)
- Gene: CNTNAP2
- Tatyana Gnedich, translated "Don Juan" while in Stalin's prison
- ?Terminal ileitis
- "Most lesions detected in the terminal ileum resolve completely spontaneously without treatment, while a few TI ulcers are associated with significant diseases such as intestinal tuberculosis or Crohn’s disease" https://bmcgastroenterol.biomedcentral.com/articles/10.1186/s12876-021-01866-7
- ?Branched-chain α-keto acid dehydrogenase kinase deficiency and autism
- Shorter name: BCKDK deficiency
- Mentioned in this 2020 CC-BY review of metabolism defects in autism
- ?Long-chain fatty-acid oxidation disorders
- ?Hypoketotic hypoglycaemia
- for instance, in long-chain fatty-acid oxidation disorders
- ?DDX3X syndrome, developmental delay
- ??ERIraos, early detection of psychosis
- Delta brush -- EEG pattern in neonates, esp. premature
- ?Extreme delta brush - in anti-NMDAr encephalitis
- Faciobrachial dystonic seizure in LGI1 encephalitis
- LGI1-antibody encephalitis
- See LGI1
- ??Individual alpha peak frequency - in ADHD, prediction of treatment success
- ??Cobalamin C deficiency -- is it the same as Methylmalonic acidemia?
- Yes, a subtype due to defects in the gene MMACHC
- Case report with "catatonic depression" and hallucinations
- Case series of psychiatric symptoms in late onset CblC deficiency.
- OMIM 277400
- ??Limbal stem cell deficiency, Corneal epithelial stem cell deficiency
- ?Benign pancreatic hyperenzymemia, or Gullo syndrome
- Macroamylasemia
- Homocystinuria-megaloblastic anemia, cblG complementation type - mutations of methionine synthase
- Beads task - The beads task (Phillips & Edwards, 1966) is an experimental task designed to examine individuals' reasoning style under ambiguous conditions.
- Urrets-Zavalia syndrome
- ?Washington Early Recognition Center Affectivity and Psychosis, or WERCAP, a screening test for schizophrenia
- ?Adiponectin deficiency
- Ventricular puncture
- ??Yale Control Over Perceptual Experiences (COPE) Scales
- ?Effort Expenditure for Reward Task (EffERT)
- ?Multiple acyl–coenzyme A dehydrogenation deficiency, improved by riboflavin
- ??Peters Delusion Inventory
- ??Whisker trimming, Bilateral whisker trimming in model mice; neuroscience
- ?RBMX2 - could be associated with rare familial bipolar disorder
- ??16p11.2 deletion syndrome - assoc. w/ autism; lipid FAM57B gene may be infolved in psychiatric dysfunction
- ??Allyn Walker, pedophilia researcher ("A Long, Dark Shadow: Minor-Attracted People and Their Pursuit of Dignity")
- ???Stellage ganglion block as a standalone? Interesting.
- ??Campana cell, Campana cells - retinal interneurons allegedly discovered in late 2021
- ??Stanford neuromodulation therapy for depression
- ?Biondi bodies -- (Biondi bodies (the “silver rings of Biondi”) are filamentous, ring-like or arc-like structures in the epithelium of the choroid plexus)
- ?General alexithymia factor score - condensed Toronto Alexithymia Scale for autistic patients
- ?Amylase awakening response - Changed in anxiety disorders
- ?Epiplexus cell, Kolmer cell of the choroid plexus
- ?Carnitine deficiency - has multiple causes
- ??Food-dependent Cushing's syndrome as a separate article, linked to KDM1A?
- ?Hyperamylasemia as a separate article, based on reviews?
- NEDHSIL - severe autism, gene: MEF2C
- ??Small dense LDL
- mild non-BH4-deficient hyperphenylalaninemia - see DNAJC12
- Poretti–Boltshauser syndrome, mutations of the LAMA1 gene
- ??CIC-rearranged sarcoma, a subset of Ewing-like sarcomas
- ??Dietary Inflammatory Index, or DII
- ??Progressive Encephalomyelitis With Rigidity and Myoclonus, PERM syndrome
- ?Familial hyperkalemic hypertension - mutations in CUL3
- Anterior capsulotomy (psychosurgery), Anterior capsulotomy for OCD
- Megalencephalic leukoencephalopathy with subcortical cysts-2A, HEPACAM gene
- ?Spinocerebellar Ataxia Type 7, Spinocerebellar Ataxia 7 - assoc. w/keratoconus
- ?Branched-chain ketoacid dehydrogenase kinase deficiency - see BCKDK; assoc. w/autism
- ??Cerebral creatine deficiency syndromes -- assoc. with autism-s-d
- ??Representational drift (in neuroscience)
- ?Per2AS, noncoding gene of sleep/wake cycle in mice
- Carol Donner author of The Magic Anatomy Book
- ?Encephalitis with Anti-SOX1 Antibodies, Anti-SOX1 encephalitis
- ??Ketamine bladder syndrome
- ???Carbonyl stress - or is it covered in Reactive carbonyl species?
- Traboulsi syndrome - corneal issues
- ??Anticholinergic cognitive burden score, ACB score
- ??Alpers-Huttenlocher syndrome - is the same as Alpers disease?
- ??DDX3X-Related Neurodevelopmental Disorder
- ??Presence hallucinations in Parkinson's
- Metzincin, or Metzincin family of enzymes
- Duplication 9p, 9p duplication syndrome
- ADAMTSL family
- ??Ewing-like sarcoma
- ??CIC-DUX4 fusion sarcoma
- Hypothyroid myopathy - Hoffman's syndrome in adults case
- OGT-linked Congenital Disorder of Glycosylation (OGT-CDG) discovered in 2021
- ??Monocyte-to-HDL-cholesterol ratio (MHR), elevated in keratoconus
- ?Phenylalanine deficiency - iatrogenic condition resulting from strict Phe-restricted diet -- Case (2013)
- ??BH4 loading test, not sure
- ?Pterin-4-alpha-carbinolamine dehydratase deficiency, a form of BH4 deficiency
- ?Miners' nystagmus - early 20th century
- Protocadherin 19, PCDH19
- Mitochondrial folate transporter or SLC25A32 - OMIM 138840,
- ??Riboflavin-responsive exercise intolerance (single patient, OMIM 616839)
- First case: 14 yo girl (2016)
- New case in a 52 yo patient (2017)
- Three patients (2021)
- ??Riboflavin-responsive exercise intolerance (single patient, OMIM 616839)
- ??pseudo-methylenetetrahydrofolate syndrome induced by folic acid overdose
- ?Syndrome of Irreversible Lithium-Effectuated Neurotoxicity
- ?Childhood Trauma Questionnaire
- ??Large neutral amino acids relevant to BH4 deficiency, PKU
- Seymour Kaufman (1924-2009), biochemist, discoverer of BH4
- DNAJC12 deficiency - OMIM 617384
- ?Phenylalanine loading test can be used to detect disorders of metabolism presenting BH4 without HPA
- ?Masaya Segawa (1936-2014) - Segawa disease, GTP cyclohydrolase I deficiency
- ??phenylalanine loading test
- 5,10-Methenyltetrahydrofolate synthetase - deficiency of this reminds of CFD
- Pierson syndrome
- Howard Allen Pearson (-2016)
- Newcastle Mitochondrial Disease Ratings Scale after the city
- LIC syndrome -- NSMCE3 gene
- Fried syndrome assoc. w/mutations in AP1S2 (a gene assoc with a case of Cerebral folate deficiency)
- ?Reversal learning - тест на переучивание навыка
- ?Spadin - Spadin is a synthetic peptide derived from sortilin which was shown to block TREK-1 with high affinity. Spadin antidepressant activity appears to be mediated through PI3K and Akt activation.
- Riboflavin transporter deficiency or Riboflavin transporter deficiency neuronopathy
- see Brown–Vialetto–Van Laere syndrome - the same
- Thiamine-responsive basal ganglia disease (source) OMIM
- NEDAMSS syndrome described in 2018
- ?Bronchodilator reversibility test in COPD
- ?The Wessler test in animals has been used extensively for over 40 years as a laboratory measure of in vivo hypercoagulability.
- ?Intra-Extra Dimensional Set Shift - a take on the Wisconsin Card Test
- ??Chorioretinal atrophy associated with Cerebral folate deficiency in one case report.
- focal electrically administered seizure therapy, or FEAST
- Separate Theta-burst stimulation or TBS
- ?Reward positivity potential, or RewP
- Pierson syndrome OMIM 60949
- ?Familial temporal lobe epilepsy, esp. type 7 assoc with RELN
- Harel-Yoon syndrome
- ?Luft disease - the rarest yet the earliest to be described
- CAD deficiency
- Hydromethylthionine - used to treat dementia
- ?Noncoring needle (Huber needle)
- cblC type methylmalonic acidemia, CblC type methylmalonic acidemia
- Tyrosine hydroxylase deficiency - associated (?) with cerebral folate deficiency? case report, case report
- ???Folate-binding proteins assay
- ??Unmetabolized folic acid might be harmful in excess
- ?Methylcobalamin deficiency complementation group G OMIM 250940
- also called Homocystinuria-megaloblastic anemia, cblG complementation type
- Caused by mutations of Methionine synthase
- ?Disorders of intracellular cobalamin metabolism
- ?Uchida-Kraepelin test requires focused effort and attention
- ?Autosomal dominant adult-onset demyelinating leukodystrophy - linked to Lamin B1 mutations, OMIM 169500
- ?Lamin B1 deficiency - in rare cases, depression? (Lisa Pan)
- Deep anterior lamellar keratoplasty
- ?STXBP1 syndrome
- ??Dysfunctional Attitude Scale
- ?Red blood cell folate - an indicator of the folate status
- Adaptinopathy such as the Pettigrew syndrome
- Pyridoxamine 5′-phosphate oxidase (PNPO) deficiency
- DNAJC12-deficient hyperphenylalaninemia
- Glutamate formimidoyltransferase deficiency - elevated folates
- MTHFD1 deficiency - rare; may cause cerebral folate deficiency
- MTHFS deficiency - very rare, only two cases by 2019
- GTP-cyclohydrolase deficiency - a single case of treatment-resistant depression
- ?5,10-methenyltetrahydrofolate synthetase deficiency
- ?Brittle cornea syndrome
- ?Methylfolate trap hypothesis - гипотеза метилфолатной (фолатной) ловушки
- ?Dihydropteridine reductase deficiency - accompanied by Cerebral folate deficiency (PMID 30916789)
- ?Serine deficiency syndromes - a cause of Cerebral Folate Deficiency?
- ?BK virus nephropathy in kidney transplant cases
- Pettigrew syndrome
- ??Zinc and depression - similar to Magnesium and depression
- SLC39A8 - zinc transporter associated with schizophrenia 2019 news
- ??LA-DGLA ratio - zinc status test (with the colon between them, not the dash)
- ???Leucovorin rescue - I'd like to understand how and why it works exactly, and describe the mechanism
- Tsukushi proteoglycan, a member of the secreted small leucine-rich repeat proteoglycan (SLRP) family
- ??? Something about GRIN2A-related disorders?
- ??Dihydrofolate reductase deficiency - associated with cerebral folate deficiency PMID 21310277
- Glutamate formiminotransferase deficiency - OMIM #229100, folate metabolism
- " is the second most common of the known inherited disorders of folate metabolism" 18 cases
- faciobrachial dystonic seizures (FBDS)
- ?Autosomal dominant lateral temporal epilepsy (ADLTE) - some cases associated with mutations of Reelin
- Functional methionine synthase deficiency - CblE and CblG defects, related to folate metabolism
- GTP cyclohydrolase I deficiency - severe depression healed by tetrahydrobiopterine analogue
- ??Small extracellular vesicle, from PMID 30535257
- ???Magnesium load test (chronic latent magnesium deficiency - does it exist?)
- ???Sleep variability
- ?Polycythemia-paraganglioma-somatostatinoma syndrome established in 2016, HIF2alpha gene (source)
- ?Urinary metanephrines test for pheochromocytoma diagnosis
- Sheehan Disability Scale
- Iowa singing social stress test - compare with Trier social stress test
- Withanoside IV from Ashwagandha promotes memory via the RET oncogene.. yikes
- ?Continuous recognition task (CRT); persons with disrupted orbitofrontal cortices make errors in repeated CRT (rCRT)
- ??KINARM test of brain function
- ??Selective reminding test
- Descemet's membrane endothelial keratoplasty
- ??DEX/CRH test - an alternative to the Dexamethasone suppression test
- ??Postoperative delirium
- ?LGI1 encephalitis (a limbic encephalitis)
- ???Chromaffin tumour - with links to Pheochromocytoma and Paraganglioma
- ???Subclinical Cushing's syndrome
- ??Isolated adrenocorticotropic hormone deficiency
- ??Factitious Cushing's syndrome
- ?Secondary hypothermia
- Urinary free cortisol
- Ectopic Cushing's disease - make a standalone
- Inferior petrosal sinus sampling - make a standalone article
- ?Desmopressin test, DDAVP challenge - used to help differentiate between Cushing's syndrome\disease and pseudo-Cushing's
- Subclinical hypercortisolism
- Ureterovesical junction obstruction
- Outer radial glia
- Posterior keratoconus - see the review
- Elovanoid
- ?Deglycosylation of proteins and antibodies, for instance, by PNGase F
- ?Taganay National Park
- ?Vacuum blotting (in electrophoresis)
- ?A-tailing (genetics)
- ?Soybean casein digest medium
- ?Isoenzyme Analysis
- ?2-delta-delta-CT Method in real-time PCR
- ?Freezing point depression osmometer
- ?WEHI-13VAR cell culture used to assess TNF-alpha activity
- ?Data-dependent acquisition (mass-spectrometry)
- ?Paraffin film
- ?Capillary isoelectric focusing, cIEF
- ?Perfusion bioreactor
- ?Pipette tip solid-phase extraction
- ?Relative standard curve method
- ?Isolation of mononuclear cells from blood by centrifugation
- ?Isotype control antibody, or simply Isotype control
- ?Cascade immunization for detecting host cell protein (residual)
- ?Host cell protein analysis using CHO (hamster ovarian cell lines)
- ?Membrane filtration method in Ph.
- ?Direct inoculation method in pharmacopoeia
- ??Mixed melting point - a technique in analytical chemistry
- ??External standard - a calibration method on par with Standard addition and Internal standard (HPLC)
- ?Bioequivalence study - ru:Исследование биоэквивалентности
- ?Sulfated ash and Residue on ignition (pharma)
- ?Robustness test (in analytical method validation)
- ?Syndrome of pituitary resistance to thyroid hormone, Syndrome of PRTH
- Cavernous sinus syndromes
- ?Reverse pseudohyperkalemia
- ?Vertical lathe - ru:Карусельный станок
- Plug rolling process, also Stiefer rolling process, after its inventor R. C. Stiefel - ru:Горячая прокатка труб на оправке
- Flying shears - ru:Летучие ножницы
- Pilger mill - ru:Пилигримовый стан
- Fretz-Moon process - production of pipes
- ?? cortisol/DHEAS-ratio - high in treatment-resistant depression
- ru:Оленьи Ручьи - Olenii Ruchii (Park, Russia)
- (??) Ectopic ACTH syndrome
- ru:Климзо, Борис Николаевич - Boris Klimzo, translator
- ?Sodium tetrahydroxoaluminate
- ru:Восточно-Уральский заповедник - East Urals Nature Reserve (nuclear contamination area)
- ?Fohl's test to detect sulfur-containing amino acids
- 1-ethoxypropane or Ethyl propyl ether
- ?Inorganic esters as a standalone article
- Kucherov reaction (from redir) - ru:Реакция Кучерова (acetylene to acetaldehyde using HgSO4)
- ru:Павлов, Михаил Александрович- Mikhail Alexandrovich Pavlov
- ??Thr92Ala polymorphism of DIO2
- SLCO1C1 - transports the thyroid hormone T4 across the BBB into the brain. (OMIM)
- ?Corneal biomechanics - hysteresis, resistance factor, etc.
- ?Whickham Survey (thyroid disorders)
- ?Myoedema - hypothyroidism
- ?Hoffman syndrome Hoffman's syndrome- in hypothyroidism
- ?Oxidative Stress Index
- Laser-Induced Forward Transfer (LIFT)
- Laser-Assisted Bioprinting, Laser-assisted bioprinting
- May Walk - ru:Майская прогулка
- Mikhail Semiryaga - ru:Семиряга, Михаил Иванович (WWII, germany, diplomacy)
- ?George Magnus - "the age of aging"
- ?1977 Constitution of Afghanistan - abrogated following the Zaur Revolution (27 April 1978)
- ???Ramamoorthy Gopalakrishnan - "The Geography and Politics of Afghanistan" (1983)
- Mikhail Ionov - ru:Ионов, Михаил Ефремович - military expeditions to the Pamir region in the 1890s
- Alexey Levinson - ru:Левинсон, Алексей Георгиевич (sociologist)
- ??Afghanistan's provincial councils - exist from 2005
- Henry E. Hale - Russian studies
- National Ulema Council of Afghanistan
- Karategin - ru:Каратегин - hist. independent part of Tajikistan; site of insurgency in 1990s
- Mirzo Zieev (died 2009) - former Tajik Emergency Minister said to be linked to IMU
- Islamic Committee of Russia - ru:Исламский комитет России
- Uwe Halbach - de:Uwe Halbach
- State Commission for Religious Affairs of Kyrgyzstan
- ??Kathrin Lenz-Raymann - "Securitization of Islam" (Central Asia, 2015)
- Kathleen Collins (author) - "Clan Politics and Regime Transition in Central Asia"
- Regional Anti-Terrorist Structure of the SCO
- ru:Чёрный тюльпан (Екатеринбург) - Black Tulip (monument)
- Ministry of North Caucasus Affairs, Minkavkaz - ru:Министерство Российской Федерации по делам Северного Кавказа (from 2014)
- ??Nogai Batallion - ru:Ногайский батальон
- and the upplaced Vilayat Nogay steppe
- Abbas Kebedov - ru:Кебедов, Аббас Кебедович a founder of the 1990 IRP
- Bagauddin Kebedov - ru:Кебедов, Багаутдин Магомедович - ideologue of Dagestani Islamist militancy
- Alexander Alexandrovich Ignatenko - ru:Игнатенко, Александр Александрович (Islam expert)
- ?? Ahlu Sunna - ru:Ахлю Сунна (Дагестан, салафиты)
- Paul J. Murphy - "Wolves of Islam"
- Matthew Evangelista - "Chechen Wars" (2002)
- ?Stephen R. Bowers - post-USSR, North Caucasus studies
- Chechen presidential election, 1997
- Chechen presidential election, 2004
- ?Yoav Karny (Yo'av Karny) - author of articles and one book on Chechnya (Highlanders)
- Chabanmakhi - ru:Чабанмахи
- Alexei Malashenko - ru:Малашенко, Алексей Всеволодович (ru Islam researcher)
- Jamaat Ansarullah, Tajikistan
- Nadir Khachilayev - Russia's Muslim Union
- National Strategy Institute (Russia);
- Rustam Burnashev - good articles on Central Asia
- Adeeb Khalid - de:Abeeb Khalid - history of Central Asia since 1860
- Naum Nim - ru:Ним, Наум
- National Counterterrorism Committee (Russia) (established in February 2006)
- Walter Reich - author of "Origins of Terrorism" (1990)
- Kirill Nourzhanov - author of Tajikistan: a political and social history (2013)
- Tajikistan's National Reconciliation Commission 1997-2000
- 1997 Tajikistan Peace Agreement - "General Agreement on the Establishment of Peace and National Accord in Tajikistan"
- Kokand Autonomy - ru:Туркестанская автономия
- Kamoludin Abdullaev Камолуддин Абдуллаев - Tajik historian
- Usman Ghazi - IMU leader (?)
- Free Russia Foundation
- Oinihol Bobonazarova - human rights, Tajikistan
- Mullo Abdullo Rakhimov - Islamist militant killed in Tajikistan
- Tajikistan Council of Ulems or Shuroi Ulamo
- People's Front of Tajikistan, or Popular Front of Tajikistan (c.war 1992-7)
- 1877 Chechnya and Dagestan uprising - ru:Восстание 1877 года в Чечне и Дагестане
- Lena Jonson - books on Central Asia
- Batken events (1999) - ru:Баткенские события
- People's Movement of Uzbekistan - 28 May 2011, Berlin
- Islamic Renaissance Party (Astrakhan, 1990-1992 (or 1994?))
- Akhmet Yarlykapov - Caucasus expert - ru:Ярлыкапов, Ахмет Аминович
- Mairbek Vatchagaev - Chechen historian, Maskhadov rep., several books
- Yavus Akhmadov - Chechen historian - ru:Ахмадов, Явус Зайндиевич
- Emil Souleimanov - auhtor on Chechen modern history
- ru:Межвоенный кризис в Чечне - interbellum crisis in Chechnya, Wahhabism crisis in Chechnya
- Philip Shishkin, author of "Restless Valley"
- ?Shahrbanou Tadjbakhsh - Central Asia scholar, author
- Gordon M. Hahn - "Russia’s Islamic Threat" (2007)
- Jeffrey Haynes - books on religious movements and international relations
- Pierre-Arnaud Chouvy - "Opium"
- Alexander Marshall - Glasgow Uni., author of "Afghanistan: How the West Lost Its Way"
- ?Afghanistan-Central Asia Dialogue
- David Mansfield (author) - author on Afghanistan
- Caspian Anti-Drug Five, Central Asian Anti-Drug Quartet
- Sebastien Peyrouse, author of books on Central Asia
- George Gavrilis, author of "The Dynamics of Interstate Boundaries", articles on Central Asia
- Central Asia Drug Action Programme (CADAP)
- Matvei Shaposhnikov - ru:Шапошников, Матвей Кузьмич (refused to use tanks during the Novocherkassk protests in 1960s
- Alexander Knyazev - ru:Князев, Александр Алексеевич
- Vasili Tyorkin
- Border Management Programme in Central Asia (BOMCA)
- Istanbul Process on Regional Security and Cooperation for a Secure and Stable Afghanistan - Heart of Asia Process (2014 review)
- Turkmenistan-Afghanistan-Tajikistan Railway
- 3 Hut Uprising - Kabul, February 22, 1980
- Rein Müllerson - author of books on Central Asia
- ru:Орлуша - Russian poet
- CASA-1000 electricity project
- Depictive construction, Depictive predicate - see Secondary predicate
- Beads task - Jumping to conclusions; metacognitive
- ?Salience attribution test, SAT
- ?Amylase/Creatinine Clearance Ratio - helpful in pancreatitis DDx
- ?Hyperamylasemia, a standalone page
- ?Mitokine - inter-mitochondrial signal (putative yet?)
- ?Cocaine-induced leukoencephalopathy - see Levamisole
- ru:Хивинский поход (1839—1840) - Khiva Campaign (1839-1840)
- EXBS, Export Control and Related Border Security program
- ru:Бой на 12-й заставе Московского погранотряда -
- ru:Группа Пограничных войск России в Республике Таджикистан
- Helmand River Water Treaty Iran / Afghanistan, 1973-75
- Urrets-Zavalia syndrome - questioned by some; linked to keratoconus
- Wallis and Matilda - marv Aussie folk band (Pioneers album/Banjo Pat.)
- Isopropylbenzene hydroperoxide - rubber production; see Cumen process
- Cerebral edema in diabetic ketoacidosis, CEDKA
- Glycated albumin - a rival of Hb1ac
- Specular microscope - used to visualize corneal endothelium
- TGF-beta signalopathies share the mechanism with the Marfan syndrome
- ?Primary angiitis of the central nervous system, PACNS
- ?Status dissociatus
- Blistering, a quaint treatment for madness in 1800s
- multiple pituitary hormone deficiency, MPHD - genes PROP1 or Pit1 (also called POU1F1)
- HANAC syndrome
- ?Corneal hysteresis
- ?flow-mediated dilatation
- ?Granulocyte-Angiotensin System, Granulocyte-angiotensin system
- Juvenile-onset dystonia
- Baraitser-Winter Syndrome
- ?Human antigen R, or HuR, is lowered in KC
- ?sublinical hypercortisolism (->diabetes)
- ?hypercortisolism
- ?Hypothalamic hypopituitarism
- Monetary Incentive Delay Task, MID task
- amorfrutins fight the diabetes
- Brown-McLean syndrome
- ru:Человек в футляре (фильм) - Chelovek v futliare
- Vortex keratopathy
- Cerebral hyperperfusion syndrome
- ?Postprandial hypotension
- Ophelia syndrome = Hodgkin's lymphoma + Limbic encephalitis
- Borjeson-Forssman-Lehmann syndrome
- Floppy eyelid syndrome
- + L-arginine: test of endothelial function
- Autoimmune Encephalopathy? - link
- maxillary sinusotomy
- ? Stress-induced hyperthermia (SIH)
- ru:Чулаки, Михаил Михайлович -
- Anti-AMPA Receptor Encephalitis
- Anti-GABA Receptor Encephalitis
- ?Idiopathic Hypothalamic Dysfunction
- ?activity-dependent neuroprotective protein, ADNP
- Neoplastic Lumbosacral Plexopathy or Neoplastic lumbosacral plexopathy or simply NLP
- ??Gordon Holmes spinocerebellar ataxia syndrome, Gordon Holmes spinocerebellar ataxia
- α-Methylacyl-CoA racemase deficiency or AMACR deficiency, see AMACR
- Adult Polyglucosan Body Disease? or just Glycogen storage disease type IV
- Mitochondrial DNA depletion syndrome (OMIM 609560, 251880); DGUOK gene
- Navajo neurohepatopathy (NNH; 256810)
- Mitochondrial myopathy with diabetes OMIM 500002
- ?Rolf Luft, MD, PhD (1914-2007)
- extremely strange Luft's disease
- a separate page for the Ragged red fibre \ Ragged red fiber?
- Edaravone for stroke-like episodes
- ?Mitochondrial DNA depletion syndrome (OMIM 251880)
- ?Mountain car problem, Mountain-car problem
- ?Alpers-Huttenlocher-like disease
- ru:Портик Нового Эрмитажа
- ?maximal cycle test PMID 8603770
- ?hyperglycemic clamp
- Chromosome 3-linked frontotemporal dementia (OMIM 600795) - CHMP2B gene
- Corneal Hysteresis?
- Ocular Response Analyzer?
- Cyclooxygenase Deficiency (see eMed)
- X-linked Leigh's syndrome\X-linked Leigh syndrome (OMIM 308930)
- ru:Ямская гоньба - ?
- ru:Шумлянский, Александр Михайлович Alexander Shumliansky
- ru:Скачет красная конница - The Red Cavalry Riding
- ru:Николашка - Nikolashka
- ?Atopic IgE responsiveness OMIM 147050
- Pyotr G. Likhachov (1758-1813) - ru:Лихачёв, Пётр Гаврилович
- ?Diadochokinetic rate
- ?minimal hepatic encephalopathy (MHE) unsure, seems to be promoted by one person (Bajaj), but interesting
- review at World J Gasto
- Indian review (2009), incl. pathogenesis
- Melatonin and sleep inversion
- ru:Китоврас - Kitovras
- ?Amitosis? - ru:Амитоз
- Trichoblasts form plant root hairs
- ..and atrichoblasts
- Initiating cell (tip of the plant root)
- Lomasome - ru:Ломасома (in fungal cells)
- ?Axon initial segment (AIS)
- ru:Змиёвская балка
- chromosome 9q subtelomere deletion syndrome (9qSTDS)
- Tonoplast intrinsic protein
- Brittle cornea syndrome OMIM 229200
- ru:Остер, Григорий Бенционович
- ru:Мемориал воинской славы (Кутаиси)
- Hapters, another kind of lichen roots
- Rhizines, Rhizoid-like lichen "roots"
- ru:Баранецкий, Осип Васильевич
- ru:Пётр Телушкин - Pyotr Telushkin
- Huntington disease-like (HDL1, HDL2, HDL3; see OMIM)
- Anti-NMDA receptor encephalitis
The disorder has received several names, including acute diffuse lymphocytic meningoencephalitis,2,3 acute reversible limbic encephalitis,4 acute juvenile female nonherpetic encephalitis,1 or juvenile acute nonherpetic encephalitis.
- pregnenolone sulfate
- Spotted cystic neovascular macular dystrophy (discovered)
- Louis-Victor Marcé PMID 2687917
- Isoallopregnanolone
- Steroid myopathy,Corticosteroid-induced myopathy, eMedicine
- Vogel's conflict test, Vogel test
- Allotetrahydrocortisol (Allo-THF)
- 3alpha-5alpha-androstan-diol, neurosteroid derivative of testosterone
- ?Maternal separation (in animals)
- adrenoglomerulotropin - ru:Адреногломерулотропин
- SKF 105,111 - 5-alpha-reductase inhibitor
- 3alpha-hydroxysteroidoxidoreductase
- ru:Уралмаш (район) - Uralmash (district)
- ru:Колпеница - Kolpenitsa
- ??dihydrophil hydratase
- ru:Однодворцы - Odnodvoretz
- ru:Онгаро, Франка
- Hereditary angioedema type III OMIM 610618
- Segawa Syndrome omim 605407
- Pitt-Hopkins Syndrome
- cholesterol sulfate
- Neurogliaform cells (source)
- Corticosterone methyloxidase type 1 deficiency (omim)
- Corticosterone methyloxidase type 2 deficiency (omim)
- ?Acute swim stress, btw: sex difference in NMDA activation, prob neurosteroid related
- AllotetrahydroDOC, a neurosteroid
- ?John Weir Perry
- ?Adrenal rest = Accessory adrenal = Marchand's adrenals = Testicular adrenal rest tissue = Testicular adrenal rest tumour (TART)
- (see Felix Jacob Marchand)
- see PMID 11739428 (high-prev. in CAH)
- see a review of rests in CAH
- Adrenal hemorrhage (?) eMedicine
- SKC mouse (keratoconus but doubtable) PMID 11773012
- isoketals, isoketal
- Neuroprostane, Neuroprostanes
- Pigmented paravenous chorioretinal atrophy
- S-nitrosocysteine, NO generator
- ??Superoxide dismutase mimetics
- ??Nitrotyrosine denitrase
- Nitrosoperoxycarbonate (catabolism of peroxynitrite)
- ?nitrotryptophan 6-nitrotryptophan
- ru:Любищев, Александр Александрович - Alexander Alexandrovich Lyubischev
- ru:Трофейные бригады - trophy brigades
- ?presynaptic active zone
- ?conserved dopamine neurotrophic factor, CDNF
- ?mesencephalic astrocyte-derived neurotrophic factor, MANF
- ?Wessely ring - Immune Ring of Wessely - Wessely immune ring
- ?Tumstatin
- ?Anastellin
- ?Cholinergic rebound
- ?middle face patch, face patch system (here)
- ?mitochondrial membrane potential
- Fluorochrome-labeled inhibitors of caspases, FLICA
- Endoplasmic reticulum stress
- Neuroferritinopathy
- Julius Hallervorden Nazi and Iron overload
- ?Neurodegeneration with brain iron accumulation (NBIA)
- Long-Evans Cinnamon rat, LEC rat, a model of Wilson's disease
- 3-Morpholinosydnonimine (SIN-1), NO release
- Sorsby's fundus dystrophy (TIMP3)
- Salzmann nodular corneal degeneration
- hyperimmunoglobulin E recurrent infection syndrome
- Emotion Recognition Task
- neuronal nuclear antigen, NeuN
- Transferrin family
- ?MTHFR deficiency (OMIM 236250)
- Sticky fixation (brain dev)
- GABA-glutamine cycle
- Scurfy mouse
- ?Lipid keratopathies (fish-eye disease etc)
- Argpyrimidine
- Synoviocyte
- Royal College of Surgeons Rat
- ?neuroectodermal sphere
- György Buzsáki
- ?Pandit Rajan and Sajan Mishra
- Goblet neuron,Goblet interneuron
- ?One-carbon metabolism
- Dystrophia Helsinglandica
- Dystrophia Smolandiensis
- ?Urrets-Zavalia syndrome
- Dependence receptor
- HOMER protein family - D'oh
- ?Corneal sensitivity, Corneal sensitivity test
- (Cochet-Bonnet aesthesiometer )
- Terrien's marginal degeneration
- mention anterior corneal mosaic?
- ? crocodile shagreen
- ? corneal hydrops
- Pattern separation (neurogenesis)
- Wavefront aberrometer, aberrometer
- Wavefront aberrometry, aberrometry
- Zoogloea ie Indian sea rice
- Endothelial keratoplasty
- Descemet Stripping Endothelial Keratoplasty, DSEK,DSAEK
- Terrien's marginal corneal degeneration or Terrien marginal corneal degeneration
- ru:Бензобарбитал - Benzobarbital
- ru:Сикорский, Иван Алексеевич-Ivan Alexeevich Sikorsky
- Antidepressant Apathy Syndrome (?)
- Corneal melt, corneal melting, Corneoscleral melting
- Neurotrophic keratopathy
- Diabetic keratopathy ?
- Joanna Moncrieff ?
- Small leucine-rich proteoglycan family, SLRP family
- Peters anomaly OMIM 604229
- Grayson-Wilbrandt dystrophy
- ? Hale's colloidal iron stain
- cribriform mesenchyme
- Lipid hydroperoxide
- α,β-unsaturated aldehydes or alpha,beta-unsaturated aldehydes or OαβUA, such as 4-HNE
- Bullous disease, autoimmune bullous disease
- dermal-epidermal junction (?)
- ? Interstitial neurons (PMID 19543540)
- anti-p200 pemphigoid
- gamma-oryzanol from Rice bran oil
- Advanced lipoxidation end-products (see AGE)
- ru:Ноль (группа) - Nol' (rock band)
- Transferrin family
- Corneal Langerhans cells (?)
- Harboyan syndrome
- ? sickness syndrome (cytokines and depression)
- Small leucine-rich proteoglycans
- Mucin ball due to CL wear
- Scheimpflug ocular imaging
- Mitochondrial oxidative stress (? PMID 18341705)
- Puerarin (NOS, inflammation?)
- epikeratoplasty
- leukocyte common antigen-related (LAR) subfamily of receptor PTPs, LAR-RPTP PMID 15674434
- Millon Index of Personality Styles (MIPS)
- neuroleptic-induced deficit syndrome (NIDS) (PMID 8866773) ?
- ru:Старик Букашкин - Old man Bukashkin
- ru:Кобрин, Владимир Михайлович Vladimir Kobrin
- ru:Игры с ножом Russian knife games
- TUR syndrome
- Polydendrocyte or NG2 cell (??)
- The Republic of SHKID
- ru:Акмолинский лагерь жён изменников Родины
- Nonsynonymous mutation (Nonsynonymous polymorphism?)
- Double bouquet cell (= fusiform cell?) Important: PMID 15846784
- DNA methyltransferase-1 - overexpressed (postmortem: PMID 17259861) in psychosis, downregulates GAD67 and Reelin in GABAergic interneurons of schizophrenia and bipolar patients.
- GABAergic interneuron - I'm not sure but there seems to be an extensive array of GABAergic interneuron subtypes - 14 subtypes according to Gupta et al, 2000. PMID 10634775
- GABA membrane transporter-1, or GAT-1 - seems to be decreased in schizophrenia.(Also: PMID 15365220) Seems also to be increased by antipsychotics in mice: PMID 15467974. There are clinical studies of GAT-1 inhibitor tiagabine as an add-on in schizophrenia: 1 2.
- or maybe just GABA transporters for a start.
- Axo-axonic cell (?)
- "Reelin and GAD67 are not the only genes whose expression is down-regulated in GABAergic neurons of SZ and BP+ patients. For example, the expression of GABA transporter (GAT1) (30), parvalbumin (25) or N-methyl-d-aspartate receptor subunits (15) is also down-regulated in GABAergic neurons of SZ and BP+ patients." [1] Got to be investigated. GAT1 and parvalbumin decrease seems to occur in disctinct GABAergic interneuron populations from the reelin-containing cells. So it seems.
- Meynert cell - a specialized pyramidal neuron of the visual cortex.
- Line bisection task (?) - used to detect visuospatial neglects.
- BHLH-PAS superfamily of transcription factors - maybe.
- Wide arbor cell (?)
- Postsynaptic density 95 or PSD95, or, more rightly, DISCS LARGE, DROSOPHILA, HOMOLOG OF, 4; DLG4
- NMDA subunit NR2A, NMDA subunit NR2B - OMIM links: 1, 2.
- Abnormal involuntary movement scale, AIMS - measuring tardive dyskinesia.
- Continuous Performance Test, Identical Pairs Version, or CPT-IP
- PirB - in cahoots with MHC class I; affects neuronal circuitry. [2]; [3].
- Antisaccade task
- P50 sensory gating test (or P50 (evoked potential)?) - lack of ihnibition in schizophrenia.
- Binocular depth inversion (?)
- Salvianolic Acid (?)
- Miraxion - artificial eicosapentaenoic acid.
- Artificial cornea (keratoprosthesis)
- Contingent Negative Variation (??)
- Maternal deprivation (??)
- visual backward masking, motion integration (PMID 17487285)
- Go-NoGo task disruption in ADHD, schizophrenia.
- KIBRA protein associated with memory performance. (OMIM)
- Kinectin, a microtubule-associated protein.
- Oculomotor delayed response task, ODR
- Etazolate, PDE inhibitor.
- trisynaptic pathway in hippocampus.
- preparing to overcome prepotency task, or POP task which is based on Simon spatial incompatibility effect
- Social defeat or social defeat stress - may be a risk factor in schizophrenia.
- Uchida-Kraepelin test(?)
- septohippocampal pathway
- RGS proteins (?)
- granular retrosplenial cortex (?)
- Sprague effect - "an unusual phenomenon known as the Sprague effect. Complete removal of the visual cortex on one side of the brain renders animals unable to see anything in the half of the visual field opposite the surgical site. Yet a tiny cut to the midbrain restores the animal's ability to detect and approach moving entities, even though it still can't distinguish one object from another."
- Herpes Encephalitis
- Maternal immune activation - behaviour changes in rodents similar to schizophrenia, autism; probably via IL-6 cytokine.
- Binding immunoglobulin protein (immunoglobulin heavy chain binding protein ), BiP, a.k.a. Grp78
- PSE-Catego (?) psychiatric diagnostic system
- Glutamate carboxypeptidase III, GCPIII
- Glucose Tolerance Factor
- fluorodopa 18F, FDOPA
- Steroid dementia, Steroid dementia syndrome
- kynurenine metabolic pathway
- 5-hydroxyindole acetic acid, or simply 5-hydroxyindole, a metabolite of tryptophan.
- Brachydactyly mental retardation syndrome, OMIM 600430
- methylazoxymethanol acetate model of schizophrenia, MAM model of schizophrenia
- methylazoxymethanol acetate
- Quinolinic acid
- dystrophin-associated protein complex, DPC
- Biogenesis of lysosome-related organelles complex 2, BLOC-2
- Biogenesis of lysosome-related organelles complex 3, BLOC-3
- Sandy (mouse) or SDY, a dysbindin knockout mouse.
- X-linked chronic granulomatous disease (caused by a mutation in NADPH oxidase subunit genes; OMIM link)
- Optogenetics (?)
- Kendler's Structured Interview for Schizotypy
- oriens-lacunosum moleculare (O-LM) interneurons
- Corticogenesis
- periventricular nodular heterotopia: In a normal brain, much of the gray matter (consisting mostly of nerve cells) appears on the brain’s surface, while white matter (consisting mostly of nerve fibers, or “wiring,” connecting areas of gray matter) runs deeper in the brain. In PNH, nodules of gray matter sit deep in the brain’s core, in the white matter; they failed to migrate out to the surface as the brain was developing.
- Forced normalization (?) - psychotic symptoms associated with seizure control in epilepsy (described here).
- Unertan syndrome - see Ulas family
- Default network (brain)
- Ivy cells of the hippocampus
- Use-dependent plasticity
- Animal models of schizophrenia
- The cytomatrix active zone (CAZ) is a specialized cellular structure regulating release of vesicles
- nail fold (nailfold plexus visibility, NPV, as a sign of schizophrenia assoc. w\neg. symp.)
- dopaminergic retrorubral field (?)
- cognitive remediation therapy, cognitive remediation
- dysgranular cortex(?)
- intermediate progenitor cells of subventricular zone which participate in adult neurogenesis.
- ventricular zone - below the SVZ; home of radial glia cells
- globuli cells of mushroom bodies
- Chromosome 3p deletion syndrome
- subpial granular layer, important transient structure.
- Poivre Atoll
- Oligodendrocyte progenitor cell
- endothelial cell density, endothelial cell count of cornea (decreased in keratoconus)
- specular microscope
- atropinic coma therapy,Atropine coma therapy
- Trail Making Test
- Mexidol
- Spidery neuron
- MEDNIK syndrome
- Interpersonal Reactivity Index
- Pink spots in schizophrenia (0:
Articles to expand and improve
- Secondary predicate
- Rickets - if "Magnesium-dependent vitamin-D-resistant rickets" is a real thing, add a mention.
- Antiphospholipid syndrome - add info on psychiatric presentations (antibodies to annexins? Annexins are linked to p11, which is implicated in depression)
Articles to improve:
- ATP6V0C - mention neurodevelopmental disorder with or without febrile seizures
- SLC7A5 - amino acid brain transporter; autism spectrum disorder (see the Talk page)
- Multiple acyl-CoA dehydrogenase deficiency - add mention of late onset cases (paper)
- GRIN1 subunit of the NMDAr: mutations -> developmental delay, seizures, ataxia (three OMIM entities)
- UBE3B - mutations cause a developmental disorder and affect BCKDK, which also causes a developmental disorder
- TMLHE - associated with autism, although with a low penetrance?
- https://pubmed.ncbi.nlm.nih.gov/25943046/ - "The patient's neurodevelopmental deficits responded favorably to oral carnitine supplementation"
- Brain carnitine deficiency causes nonsyndromic autism with an extreme male bias: A hypothesis
- PDXK mutations cause polyneuropathy responsive to PLP supplementation. Movement restored in patients.
- Hyperprolinemia type II - behavioral problems, hallucinations (review)
- PCDH19 - is cerebral folate deficiency a typical feature of PCDH19-related epilepsy? Mention, if so.
- Pay attention to the SZ-associated genes discovered in this study
- Are POLG mutations associated with cerebral folate deficiency? Mention, if so.
- Visceroptosis - add images from here
- Cerebral small vessel disease (CSVD)
- Methylenetetrahydrofolate reductase deficiency - add information on the severe (though rare) forms of the disease (review in PMID 26872964 (2016)). Such forms can manifest as psychosis and mental degradation accompanied by seizures. Very interesting.
- MODY 2 - very interesting
- Folate deficiency - add section on cerebral folate deficiency assoc. with catatonia and other psych symptoms
- Hereditary folate malabsorption - read, investigate
- Paraganglioma - add mention of "cluster 1" and "cluster 2" (genetics-based classification)
- Cushing's syndrome - add description of the cyclic\intermittent Cushing's syndrome review here 2007
- Cell bank
- Microcarrier - used for growing cells in bioreactors;
- Dilution cloning
- Microextrusion
- Corticogenesis
- Zinin reaction
- Thiocyanatoiron - hydrated form
Would be great to translate:
Articles I've contributed to
Acceptability of sources in medical articles
- WP:MEDRS - on acceptable sources.
- WP:WHYMEDRS - background
- WP:MEDFAQ - draft on when primary sources might be useful
Questionable sources
- Wikipedia:Finding images tutorial
- Wikipedia:Copyright_assistance
- Wikipedia:Image use policy
- Wikipedia:Wikimedia sister projects
- Portal:Neuroscience
- Portal:Mind and Brain
- WikiProject Russia
- Portal:Artificial_intelligence
- HTML-to-Wiki converter
- WikiEd
- Wikipedia:Citing_sources
- Template:Cite journal
- Template:Doi
- Wikipedia:Translation
- Article traffic statistics
Tools for protein infobox
I assert to be the same user as commons:User:CopperKettle --CopperKettle 14:03, 22 February 2007 (UTC)
- Sherurcij (talk · contribs · deleted contribs · logs · filter log · block user · block log) - a thoughful self-description
- Tjo3ya (talk · contribs · deleted contribs · logs · filter log · block user · block log) Timothy Osborne, a grammarian (Stack Exchange)
- Libi Rubinsky (talk · contribs · deleted contribs · logs · filter log · block user · block log) - my sister (hi)
- TimVickers (talk · contribs · deleted contribs · logs · filter log · block user · block log) (director of MolCelBio project)
- Lilac_Soul (talk · contribs · deleted contribs · logs · filter log · block user · block log) (psychiatry, 1978, Netherlands)
- Joachimherz (talk · contribs · deleted contribs · logs · filter log · block user · block log) - Joachim Herz, neuroscience, Reelin, lipid signaling
- Psychiatrick (talk · contribs · deleted contribs · logs · filter log · block user · block log) (human rights, particularly in psychiatry)
- LittleHow (talk · contribs · deleted contribs · logs · filter log · block user · block log) - good-quality articles on neuropsychology
- User:Boghog2
- Jmh649 (talk · contribs · deleted contribs · logs · filter log · block user · block log), a Canadian Doc.
- User:EverSince
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- User:Shelbypark (history of psychiatry, asylums in Australia)
- User:Garrondo (psychologist from Spain; FA: Alz)
- Xasodfuih (talk · contribs · deleted contribs · logs · filter log · block user · block log) (neuroscience\hormones?)
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- Sphilbrick (talk · contribs · deleted contribs · logs · filter log · block user · block log) (Connecticut, Bayesian methods)
- Rajakhr (talk · contribs · deleted contribs · logs · filter log · block user · block log), critical of psychiatry
- Rjanag (talk · contribs · deleted contribs · logs · filter log · block user · block log), Chinese (?), psychology
- Wikipedia:Unusual articles
- Troškūnai - a Baltic town
- Brandy Clark - good country, sad in good way
- Marc Cohn (the cure, 1995)
- Natalie Merchant, breathtaking rendition of Gerard Manley Hopkins' poem at 17:00
- Linda Thompson (singer), nice Brit folk