pyridoxine has been researched along with Deficiency, Mental in 77 studies
4,5-bis(hydroxymethyl)-2-methylpyridin-3-ol: structure in first source
vitamin B6 : Any member of the group of pyridines that exhibit biological activity against vitamin B6 deficiency. Vitamin B6 deficiency is associated with microcytic anemia, electroencephalographic abnormalities, dermatitis with cheilosis (scaling on the lips and cracks at the corners of the mouth) and glossitis (swollen tongue), depression and confusion, and weakened immune function. Vitamin B6 consists of the vitamers pyridoxine, pyridoxal, and pyridoxamine and their respective 5'-phosphate esters (and includes their corresponding ionized and salt forms).
| Excerpt | Relevance | Reference |
|---|---|---|
| "In pyridoxine dependent epilepsy (PDE), patients usually present with neonatal seizures." | 7.88 | Pyridoxine dependent epilepsy: Is late onset a predictor for favorable outcome? ( Benoist, JF; Bok, LA; de Rooy, RLP; Halbertsma, FJ; Lunsing, RJ; Mills, PB; Plecko, B; Schippers, HM; Struijs, EA; Valence, S; van Hasselt, PM; van Spronsen, FJ; Whalen, S; Wohlrab, G, 2018) |
| "Pyridoxine-dependent epilepsy is a rare autosomal recessive disorder." | 7.69 | Glutamate in pyridoxine-dependent epilepsy: neurotoxic glutamate concentration in the cerebrospinal fluid and its normalization by pyridoxine. ( Baumeister, FA; Egger, J; Gsell, W; Shin, YS, 1994) |
| "We report intermittent seizures, lethargy, and Cohen's syndrome in a 4-year-old girl with hyper-beta-alaninemia and a partial deficiency of beta-alanyl-alpha-ketoglutarate transaminase (AKT)." | 7.69 | Pyridoxine-responsive hyper-beta-alaninemia associated with Cohen's syndrome. ( Barton, NW; Bernardini, I; Brady, RO; Higgins, JJ; Kaneski, CR, 1994) |
| "Pyridoxine-dependency is a rare autosomal recessive disorder causing a severe seizure disorder of prenatal or neonatal onset, psychomotor retardation and death in untreated patients." | 6.38 | Pyridoxine-dependent seizures, clinical and therapeutic aspects. ( Girardin, E; Haenggeli, CA; Paunier, L, 1991) |
| "In pyridoxine dependent epilepsy (PDE), patients usually present with neonatal seizures." | 3.88 | Pyridoxine dependent epilepsy: Is late onset a predictor for favorable outcome? ( Benoist, JF; Bok, LA; de Rooy, RLP; Halbertsma, FJ; Lunsing, RJ; Mills, PB; Plecko, B; Schippers, HM; Struijs, EA; Valence, S; van Hasselt, PM; van Spronsen, FJ; Whalen, S; Wohlrab, G, 2018) |
| "Pyridoxine-dependent epilepsy is a rare autosomal recessive disorder." | 3.69 | Glutamate in pyridoxine-dependent epilepsy: neurotoxic glutamate concentration in the cerebrospinal fluid and its normalization by pyridoxine. ( Baumeister, FA; Egger, J; Gsell, W; Shin, YS, 1994) |
| "We report intermittent seizures, lethargy, and Cohen's syndrome in a 4-year-old girl with hyper-beta-alaninemia and a partial deficiency of beta-alanyl-alpha-ketoglutarate transaminase (AKT)." | 3.69 | Pyridoxine-responsive hyper-beta-alaninemia associated with Cohen's syndrome. ( Barton, NW; Bernardini, I; Brady, RO; Higgins, JJ; Kaneski, CR, 1994) |
| " Methionine restriction initiated neonatally prevented mental retardation, retarded the rate of lens dislocation, and may have reduced the incidence of seizures." | 3.67 | The natural history of homocystinuria due to cystathionine beta-synthase deficiency. ( Andria, G; Boers, GH; Bromberg, IL; Cerone, R; Levy, HL; Mudd, SH; Pettigrew, KD; Pyeritz, RE; Skovby, F; Wilcken, B, 1985) |
| "Pyridoxine-dependency is a rare autosomal recessive disorder causing a severe seizure disorder of prenatal or neonatal onset, psychomotor retardation and death in untreated patients." | 2.38 | Pyridoxine-dependent seizures, clinical and therapeutic aspects. ( Girardin, E; Haenggeli, CA; Paunier, L, 1991) |
| "Homocystinuria was diagnosed in 15 (0." | 1.29 | Clinical and biochemical studies in homocystinuria. ( Das, GP; Kabra, M; Kaur, M; Suri, M; Verma, IC, 1995) |
| "Homocystinuria was studied in 27 patients from 15 families in New South Wales." | 1.26 | Homocystinuria in New South Wales. ( Turner, G; Wilcken, B, 1978) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 65 (84.42) | 18.7374 |
| 1990's | 5 (6.49) | 18.2507 |
| 2000's | 6 (7.79) | 29.6817 |
| 2010's | 1 (1.30) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| de Rooy, RLP | 1 |
| Halbertsma, FJ | 1 |
| Struijs, EA | 1 |
| van Spronsen, FJ | 1 |
| Lunsing, RJ | 1 |
| Schippers, HM | 1 |
| van Hasselt, PM | 1 |
| Plecko, B | 1 |
| Wohlrab, G | 1 |
| Whalen, S | 1 |
| Benoist, JF | 1 |
| Valence, S | 1 |
| Mills, PB | 1 |
| Bok, LA | 1 |
| CORBO, S | 1 |
| McGEER, EG | 1 |
| TISCHLER, B | 2 |
| HIRTZ, G | 1 |
| JIMENEZESPINOSA, L | 1 |
| LOPEZROSAT, V | 1 |
| GUARDIOLAPLA, J | 1 |
| KOHLMANN, T | 1 |
| RETT, A | 1 |
| COCHRANE, WA | 1 |
| VERGA, G | 1 |
| HOTTINGER, A | 1 |
| BERGER, H | 1 |
| KRAUTHAMMER, W | 1 |
| Baynes, K | 1 |
| Farias, ST | 1 |
| Gospe, SM | 1 |
| Buoni, S | 1 |
| Di Bartolo, RM | 1 |
| Molinelli, M | 1 |
| Palmeri, S | 1 |
| Zannolli, R | 1 |
| LEVI, S | 1 |
| FALORNI, ML | 1 |
| Alkan, A | 1 |
| Kutlu, R | 1 |
| Aslan, M | 1 |
| Sigirci, A | 1 |
| Orkan, I | 1 |
| Yakinci, C | 1 |
| Rankin, PM | 1 |
| Harrison, S | 1 |
| Chong, WK | 1 |
| Boyd, S | 1 |
| Aylett, SE | 1 |
| PENTA, P | 1 |
| Frimpter, GW | 1 |
| Greenberg, AJ | 1 |
| Hilgartner, M | 1 |
| Fuchs, F | 1 |
| Perry, TL | 2 |
| Robinson, GC | 1 |
| Teasdale, JM | 1 |
| Hansen, S | 2 |
| Goldsmith, LA | 1 |
| Schoonderwaldt, HC | 1 |
| Boers, GH | 2 |
| Cruysberg, JR | 1 |
| Schulte, BP | 1 |
| Slooff, JL | 1 |
| Thijssen, HO | 1 |
| Gualtieri, CT | 1 |
| Golden, RN | 1 |
| Fahs, JJ | 1 |
| Coburn, SP | 2 |
| Schaltenbrand, WE | 1 |
| Mahuren, JD | 1 |
| Clausman, RJ | 1 |
| Townsend, D | 1 |
| Ellman, G | 3 |
| Silverstein, CI | 2 |
| Zingarelli, G | 2 |
| Schafer, EW | 1 |
| Silverstein, L | 1 |
| Baumeister, FA | 1 |
| Gsell, W | 1 |
| Shin, YS | 1 |
| Egger, J | 1 |
| Higgins, JJ | 1 |
| Kaneski, CR | 1 |
| Bernardini, I | 1 |
| Brady, RO | 1 |
| Barton, NW | 1 |
| Kaur, M | 1 |
| Kabra, M | 1 |
| Das, GP | 1 |
| Suri, M | 1 |
| Verma, IC | 2 |
| Kodentsova, VM | 1 |
| Vrzhesinskaia, OA | 1 |
| Kharitonchik, LA | 1 |
| Vodiasova, NA | 1 |
| Iakushina, LM | 1 |
| Spirichev, VB | 1 |
| Matsumura, R | 1 |
| Burd, L | 1 |
| Stenehjem, A | 1 |
| Franceschini, LA | 1 |
| Kerbeshian, J | 1 |
| Grimm, U | 7 |
| Knapp, A | 7 |
| Schmitz, W | 7 |
| Smetan, M | 5 |
| Schmitz, KW | 5 |
| Reddemann, H | 4 |
| Schulz, M | 6 |
| Schlenzka, K | 3 |
| Siva Sankar, DV | 1 |
| Wilcken, B | 2 |
| Turner, G | 1 |
| Springer, NS | 1 |
| Fricke, NL | 1 |
| Schlenska, K | 1 |
| Machill, G | 1 |
| Haenggeli, CA | 1 |
| Girardin, E | 1 |
| Paunier, L | 1 |
| McDaniel, KD | 1 |
| Hestnes, A | 1 |
| Borud, O | 1 |
| Lunde, H | 1 |
| Gjessing, LR | 1 |
| Salfi, M | 1 |
| Mudd, SH | 1 |
| Skovby, F | 1 |
| Levy, HL | 2 |
| Pettigrew, KD | 1 |
| Pyeritz, RE | 1 |
| Andria, G | 1 |
| Bromberg, IL | 1 |
| Cerone, R | 1 |
| Chanowitz, J | 1 |
| Ganger, E | 1 |
| Teichmann, H | 1 |
| Knaape, HH | 1 |
| Love, DL | 1 |
| Crawford, LE | 1 |
| Seidenberg, M | 1 |
| Shaw, KN | 1 |
| Lieberman, E | 1 |
| Koch, R | 1 |
| Donnell, GN | 1 |
| Murphy, JV | 1 |
| Sabater, J | 1 |
| Ricós, C | 1 |
| Schulze, M | 1 |
| Wolfram, G | 1 |
| Gröbe, H | 2 |
| Palm, D | 1 |
| Müller, KM | 1 |
| AvRuskin, TW | 1 |
| Kang, ES | 1 |
| Notermans, SL | 1 |
| Blazsó, S | 1 |
| Carson, NA | 1 |
| Dunn, HG | 1 |
| Dolman, CL | 1 |
| Hagge, W | 1 |
| Tang, TT | 1 |
| Good, TA | 1 |
| Dyken, PR | 1 |
| Johnsen, SD | 1 |
| McCreadie, SR | 1 |
| Sy, ST | 1 |
| Lardy, HA | 1 |
| Rudolph, FB | 1 |
| Crawhall, JC | 1 |
| Bir, K | 1 |
| Purkiss, P | 1 |
| Stanbury, JB | 1 |
| Campos Júnior, Mde S | 1 |
| Hoineff, S | 1 |
| Broyer, M | 1 |
| Berger, R | 1 |
| Ekelund, H | 1 |
| Gamstorp, I | 2 |
| Von Studnitz, W | 1 |
| Scott, CR | 1 |
| Dassell, SW | 1 |
| Clark, SH | 1 |
| Chiang-Teng, C | 1 |
| Swedberg, KR | 1 |
| Dubois, B | 1 |
| Balmelle, J | 1 |
| Fontaine, G | 1 |
| Sinclair, S | 1 |
| Tada, K | 2 |
| Yokoyama, Y | 2 |
| Nakagawa, H | 2 |
| Yoshida, T | 1 |
| Arakawa, T | 2 |
| Neu, W | 1 |
| Kelly, S | 1 |
| Copeland, W | 1 |
| Meeuwisse, G | 1 |
| Tryding, N | 1 |
| Heeley, AF | 2 |
| Piesowicz, AT | 1 |
| McCubbing, DG | 2 |
| Bartsocas, CS | 1 |
| Crawford, JD | 1 |
| Thier, SO | 1 |
| Breakey, WR | 1 |
| Shepherd, J | 1 |
| Berlow, S | 1 |
8 reviews available for pyridoxine and Deficiency, Mental
| Article | Year |
|---|---|
[PYRIDOXINE IN THE PATHOGENESIS AND THERAPY OF NEUROLOGIC AND PSYCHIATRIC DISEASES].
Topics: Alcoholism; Brain Diseases; Chorea; Extrapyramidal Tracts; Genetics, Medical; Humans; Intellectual D | 1963 |
Pyridoxine-dependent seizures and cognition in adulthood.
Topics: Adult; Agenesis of Corpus Callosum; Anticonvulsants; Cognition Disorders; Electroencephalography; Ep | 2003 |
Tyrosinemia II: lessons in molecular pathophysiology.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Animals; Ascorbic Acid; Child; Child, Preschool; E | 1983 |
New developments in pediatric psychopharmacology.
Topics: Adolescent; Adult; Aggression; Anorexia Nervosa; Antidepressive Agents, Tricyclic; Autistic Disorder | 1983 |
[Homocystinuria].
Topics: Central Nervous System Diseases; Diagnosis, Differential; Homocystinuria; Humans; Infant, Newborn; I | 2000 |
Nutrition and drug therapy for persons with developmental disabilities.
Topics: Anticonvulsants; Antidepressive Agents; Appetite; Dextroamphetamine; Drug-Related Side Effects and A | 1975 |
Pyridoxine-dependent seizures, clinical and therapeutic aspects.
Topics: Female; Humans; Infant; Infant, Newborn; Intellectual Disability; Pyridoxine; Seizures | 1991 |
[Hypsarrhythmia].
Topics: Brain Diseases; Child; Child, Preschool; Cortisone; Diagnosis, Differential; Electroencephalography; | 1969 |
3 trials available for pyridoxine and Deficiency, Mental
| Article | Year |
|---|---|
New developments in pediatric psychopharmacology.
Topics: Adolescent; Adult; Aggression; Anorexia Nervosa; Antidepressive Agents, Tricyclic; Autistic Disorder | 1983 |
Effect of megavitamin treatment on mental performance and plasma vitamin B6 concentrations in mentally retarded young adults.
Topics: Adolescent; Adult; Dose-Response Relationship, Drug; Female; Humans; Intellectual Disability; Intell | 1983 |
[Possibilities and limitations of influencing concentration disorders in school children with organic brain-induced reduced achievement capabilities].
Topics: Acetates; Achievement; Central Nervous System Stimulants; Cerebral Palsy; Child; Clinical Trials as | 1972 |
67 other studies available for pyridoxine and Deficiency, Mental
| Article | Year |
|---|---|
Pyridoxine dependent epilepsy: Is late onset a predictor for favorable outcome?
Topics: Age of Onset; Aldehyde Dehydrogenase; Epilepsy; Female; Genotype; Humans; Infant; Intellectual Disab | 2018 |
[Retarded children treated with combined glutamic acid and pyridoxine].
Topics: Glutamates; Glutamic Acid; Intellectual Disability; Pyridoxine; Vitamin B 6 | 1952 |
Vitamin B6 and mental deficiency; the effects of large doses of B6 (pyridoxine) in phenylketonuria.
Topics: Humans; Intellectual Disability; Phenylketonurias; Pyridoxine; Vitamin B 6 | 1959 |
[Effects of pyridoxine in the treatment of retarded mental development].
Topics: Diet, Reducing; Intellectual Disability; Pyridoxine; Vitamin B 6 | 1960 |
[THE ACTION OF B-85 ON MONGOLISM AND OTHER FORMS OF OLIGOPHRENIA].
Topics: Down Syndrome; Electroencephalography; Intellectual Disability; Meclizine; Pyridoxine | 1963 |
[CLINICAL AND PSYCHOLOGICAL STUDIES ON THE EFFECT OF PYRITHIOXIN IN BRAIN-DAMAGED CHILDREN AND ADOLESCENTS].
Topics: Adolescent; Antidepressive Agents; Brain; Brain Damage, Chronic; Brain Injuries; Cerebral Palsy; Chi | 1963 |
NUTRITION RESEARCH IN PAEDIATRICS.
Topics: Canada; Child; Diet; Diet Therapy; Epilepsy; Epilepsy, Absence; Humans; Infant; Infant Nutritional P | 1964 |
[CLINICAL OBSERVATIONS ON THE PROBLEM OF VITAMIN B 6 METABOLISM].
Topics: Body Fluids; Electroencephalography; Encephalitis; Epilepsy; Humans; Intellectual Disability; Pyrido | 1964 |
Atypical BECTS and homocystinuria.
Topics: Adolescent; Adult; Anticonvulsants; Child; Diet Therapy; Drug Resistance; Electroencephalography; Ep | 2003 |
[Psychologic tests in phrenasthenia treated with glutamic acid and pyridoxine].
Topics: Glutamic Acid; Intellectual Disability; Psychological Tests; Pyridoxine | 1950 |
Pyridoxine-dependent seizures: magnetic resonance spectroscopy findings.
Topics: Aspartic Acid; Brain Damage, Chronic; Child; Choline; Consanguinity; Creatine; Diagnosis, Differenti | 2004 |
Pyridoxine-dependent seizures: a family phenotype that leads to severe cognitive deficits, regardless of treatment regime.
Topics: Administration, Oral; Adolescent; Aldehyde Dehydrogenase; Anticonvulsants; Brain; Child; Child, Pres | 2007 |
Observations on frenasthenics treated with glutamic acid and pyridoxine.
Topics: Glutamic Acid; Intellectual Disability; Pyridoxine | 1949 |
Cystathioninuria: management.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Amniotic Fluid; Child; Child, Preschool; C | 1967 |
Concurrence of cystathioninuria, nephrogenic diabetes insipidus and severe anemia.
Topics: Anemia; Anemia, Sideroblastic; Blood Transfusion; Diabetes Insipidus; Humans; Infant, Newborn; Intel | 1967 |
Neurologic manifestations of homocystinuria.
Topics: Adult; Diagnosis, Differential; Ectopia Lentis; Female; Homocystinuria; Humans; Intellectual Disabil | 1981 |
Vitamin-mineral supplement fails to improve IQ of mentally retarded young adults.
Topics: Adolescent; Adult; Double-Blind Method; Edema; Evoked Potentials; Female; Humans; Intellectual Disab | 1984 |
Glutamate in pyridoxine-dependent epilepsy: neurotoxic glutamate concentration in the cerebrospinal fluid and its normalization by pyridoxine.
Topics: Adrenocorticotropic Hormone; Electroencephalography; Epilepsy; gamma-Aminobutyric Acid; Genes, Reces | 1994 |
Pyridoxine-responsive hyper-beta-alaninemia associated with Cohen's syndrome.
Topics: 4-Aminobutyrate Transaminase; Abnormalities, Multiple; beta-Alanine; Child; Female; Humans; Intellec | 1994 |
Clinical and biochemical studies in homocystinuria.
Topics: Child; Child, Preschool; Developing Countries; Ectopia Lentis; Female; Homocystinuria; Humans; Incid | 1995 |
[Study of the relationship between indicators of provision with vitamins B2 and B6 of children 7-10 years of age with mental retardation].
Topics: Child; Creatinine; Erythrocytes; Female; Humans; Intellectual Disability; Male; Pyridoxine; Riboflav | 1997 |
A 15-year follow-up of a boy with pyridoxine (vitamin B6)-dependent seizures with autism, breath holding, and severe mental retardation.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Anticonvulsants; Autistic Disorder; Diagnosis, Dif | 2000 |
[Tryptophan metabolism and oligophrenia (author's transl)].
Topics: Amino Acid Metabolism, Inborn Errors; Down Syndrome; Epilepsy; Hartnup Disease; Humans; Intellectual | 1978 |
[Tryptophan metabolism and oligophrenia. Part 2: Personal studies].
Topics: Adolescent; Adult; Child; Humans; Intellectual Disability; Kynurenine; Pyridoxine; Serotonin; Trypto | 1978 |
Plasma levels of folates, riboflavin, vitamin B6, and ascorbate in severely disturbed children.
Topics: Adolescent; Affective Symptoms; Ascorbic Acid; Autistic Disorder; Child; Child Behavior Disorders; C | 1979 |
Homocystinuria in New South Wales.
Topics: Adolescent; Adult; Australia; Bone and Bones; Child; Child, Preschool; Ectopia Lentis; Female; Folic | 1978 |
[Tryptophan metabolism research in oligophrenic children. 4.: Activity and possibility of activating hepatic kynureninase after vitamin B6 treatment].
Topics: Adolescent; Child; Enzyme Activation; Humans; Hydrolases; Intellectual Disability; Liver; Pyridoxine | 1975 |
[Determination of kynureninase activity in oligophrenic children with hereditary taint, before and after vitamin B6 treatment].
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child; Humans; Hydrolases; Intellectual Dis | 1975 |
Pharmacologic treatment of psychiatric and neurodevelopmental disorders in children and adolescents (Part 2).
Topics: Adolescent; Antipsychotic Agents; Autistic Disorder; Benzodiazepines; Child; Chlorpromazine; Haloper | 1986 |
Cystathioninuria in a profoundly mentally retarded woman with spastic tetraplegia, deafness and abnormal liver function tests.
Topics: Cystathionine; Deafness; Female; Humans; Intellectual Disability; Liver Function Tests; Middle Aged; | 1987 |
Vitamin B6 status measures of an institutionalized mentally retarded population.
Topics: Adult; Aspartate Aminotransferases; Energy Intake; Erythrocytes; Feeding Behavior; Humans; Instituti | 1986 |
The natural history of homocystinuria due to cystathionine beta-synthase deficiency.
Topics: Adolescent; Adult; Child; Child, Preschool; Clinical Enzyme Tests; Cystathionine beta-Synthase; Fema | 1985 |
Thyroid and vitamin-mineral supplement fail to improve IQ of mentally retarded adults.
Topics: Adult; Humans; Intellectual Disability; Intelligence; Pyridoxine; Thyroxine; Trace Elements; Vitamin | 1985 |
[Studies on tryptophan metabolism in oligophrenic children. 2. Vitamin-dependent enzyme patterns (B1, B2, B6) and excretion of the tryptophan metabolites kynurenin, xanthurenic acid, trigonellinamide, and N-methylpyridone].
Topics: Child; Female; Humans; Hydrolases; Intellectual Disability; Kynurenine; Liver; Male; NADP; Pyridoxin | 1974 |
Treatment of homocystinuria with a low-methionine diet, supplemental cystine, and a methyl donor.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Choline; Cys | 1968 |
Leukocyte pyridoxal phosphate and alkaline phosphatase in Down's syndrome and other retardates.
Topics: Adolescent; Adrenal Cortex Hormones; Adult; Aldehydes; Alkaline Phosphatase; Body Surface Area; Depr | 1969 |
Cystathioninuria.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Carcinoma, Hepatocellular; Child, Preschoo | 1967 |
Efficacy of recommended therapeutic regimens in Leigh's disease.
Topics: Brain Stem; Drug Therapy, Combination; Encephalomalacia; Glutamine; Humans; Intellectual Disability; | 1974 |
Abnormalities of tryptophan metabolism (kynurenine pathway) found in a group of 830 mentally retarded children.
Topics: Child; Child, Preschool; Chromatography, Paper; Female; Humans; Infant; Infant, Newborn; Intellectua | 1974 |
[Increased kynurenine excretion and tryptophan loading in oligophrenic children with and without familial disposition].
Topics: Administration, Oral; Adolescent; Child; Female; Humans; Intellectual Disability; Kynurenine; Male; | 1972 |
[Studies on tryptophan metabolism in oligophrenic children. 1. Results on the excretion of kynurenic acid and xanthurenic acid following administration of tryptophan and their dependence on vitamin B 6 supply].
Topics: Child; Coenzymes; Humans; Intellectual Disability; Kynurenic Acid; Pyridoxine; Tryptophan; Xanthuren | 1973 |
[Homocystinuria: clinical picture, therapy and results in 8 patients].
Topics: Body Weight; Child; Child, Preschool; Cystine; Dietary Proteins; Female; Hair; Homocystine; Homocyst | 1973 |
[Pathogenesis of cerebral damage in homocystinuria].
Topics: Brain; Brain Diseases; Cerebrovascular Disorders; Child; Electroencephalography; Epilepsy; Female; H | 1973 |
Cystathioninuria, mental retardation, and juvenile diabetes mellitus.
Topics: Adolescent; Child; Consanguinity; Cystathionine; Diabetes Mellitus; Diabetes Mellitus, Type 1; Homoz | 1974 |
[On the pharmacotherapeutic treatment of cerebral palsy. II. Treatment of oligophrenia and epilepsy].
Topics: Cerebral Palsy; Child; Child, Preschool; Chlorpromazine; Epilepsy; Epilepsy, Absence; Glutamates; Hu | 1965 |
Chemical pathology of amino acid diseases.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Chemical Phenomena; Chemistry; Child; Child | 1968 |
Necrotizing encephalomyelopathy. Report of a case with manifestations resembling Behr's syndrome.
Topics: Autopsy; Brain; Brain Stem; Cerebellar Ataxia; Child; Diagnosis, Differential; Encephalomalacia; Hum | 1972 |
[Amino acid metabolism and mental retardation].
Topics: Diet Therapy; Female; Homocystinuria; Humans; Intellectual Disability; Intelligence; Male; Methionin | 1972 |
Pathogenesis of Leigh's encephalomyelopathy.
Topics: Brain Stem; Encephalomalacia; Female; Gluconeogenesis; Glutamine; Humans; Infant; Intellectual Disab | 1972 |
Sulfur amino acids as precursors of beta-mercaptolactate-cysteine disulfide in human subjects.
Topics: Adult; Anilides; Cysteine; Diet; Dietary Proteins; Disulfides; Electrophoresis; Female; Humans; Inte | 1971 |
[Effects of gamma-aminobutyric acid combined with vitamin B6 in mentally retarded children].
Topics: Adolescent; Aminobutyrates; Child; Humans; Intellectual Disability; Pyridoxine | 1968 |
[Clinical data on a drug with a base of gamma-aminobutyric acid and vitamin B6 in the treatment of cerebral paralysis, oligophrenia and behavior disorders in children].
Topics: Aminobutyrates; Cerebral Palsy; Child; Child Behavior Disorders; Child, Preschool; Female; Humans; I | 1968 |
[Cystathioninuria].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Chromatography; Chromosome Aberrations; Chromosom | 1969 |
Apparent response of impaired mental development, minor motor epilepsy and ataxia to pyridoxine.
Topics: Amino Acid Metabolism, Inborn Errors; Ataxia; Child; Child, Preschool; Electroencephalography; Epile | 1969 |
Cystathioninemia: a benign genetic condition.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Butyrates; Child; Child, Preschool; Congeni | 1970 |
[Value of Encephabol in child neuropsychiatry].
Topics: Child; Child Behavior Disorders; Child, Preschool; Female; Humans; Intellectual Disability; Male; Py | 1970 |
Homocystinuria. Report of two cases in siblings.
Topics: Child; Cystine; Diet Therapy; Female; Folic Acid; Homocystinuria; Humans; Intellectual Disability; L | 1970 |
Vitamin B6 dependent xanthurenic aciduria.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Aspartate Aminotransferases; Autoanalysis; | 1967 |
[Results of treatment with Encephabol juice in pediatrics].
Topics: Child; Child, Preschool; Dosage Forms; Humans; Intellectual Disability; Pyridoxine; Sulfides | 1967 |
A hypothesis on the homocystinuric's response to pyridoxine.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Chemistry, Clinical; Cysteine; Homocystinuria; Hum | 1968 |
Effect of phenytoin on the tryptophan load test.
Topics: Adolescent; Age Factors; Child; Child, Preschool; Diagnosis, Differential; Epilepsy; Female; Humans; | 1968 |
The biochemical and clinical effect of pyridoxine in children with brain disorders.
Topics: Aminohippuric Acids; Child; Child, Preschool; Female; Humans; Infant; Intellectual Disability; Kynur | 1968 |
Vitamin B6 dependent xanthurenic aciduria (the second report).
Topics: Acids; Amino Acids; Aspartate Aminotransferases; Child, Preschool; Erythrocytes; Female; Humans; Hyd | 1968 |
A defect in intestinal amino acid transport in Lowe's syndrome.
Topics: Adult; Arginine; Biopsy; Carbon Isotopes; Cataract; Child, Preschool; Glaucoma; Glycine; Humans; Int | 1969 |
Tryptophan loading in tuberous sclerosis.
Topics: Adolescent; Adult; Anticonvulsants; Body Weight; Epilepsy; Female; Humans; Intellectual Disability; | 1969 |
Effect of pyridoxine on the metabolism of tryptophan and branched-chain amino acids in two mentally retarded sibs.
Topics: Child, Preschool; Female; Humans; Intellectual Disability; Isoleucine; Leucine; Male; Pyridines; Pyr | 1966 |
Studies in cystathioninemia.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Chromatography, Paper; Cystinuria; Humans; Intelle | 1966 |