homocysteine has been researched along with Intellectual Disability in 17 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 13 (76.47) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (23.53) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chatterjee, A; Chattopadhyay, A; Dutta, S; Mukhopadhyay, K; Sinha, S | 1 |
Burlina, AB; Burlina, AP; Edini, C | 1 |
Bernardino, L; Brito, AP; Fonseca, N; InĂªs, L; Santos, J; Silvestre, I; Vidal, N | 1 |
CARSON, NA; CUSWORTH, DC; DENT, CE; FIELD, CM; NEILL, DW; WESTALL, RG | 1 |
COFFEY, VP | 1 |
EFRON, ML; MACCREADY, RA; MOSER, HW; YOUNG, D | 1 |
BRENTON, DP; CUSWORTH, DC; GAULL, GE | 1 |
Hansen, S; MacDougall, L; Perry, TL; Warrington, PD | 1 |
Erbe, RW; Wang, JC | 1 |
Bassan, H; Fattal-Valevski, A; Gutman, A; Harel, S; Korman, SH; Lerman-Sagie, T | 1 |
Sviatkina, OB; Vel'tishchev, IuE | 1 |
Dillon, MJ; England, JM; Gompertz, D; Goodey, PA; Grant, DB; Hussein, HA; Linnell, JC; Matthews, DM; Mudd, SH; Newns, GH; Seakins, JW; Uhlendorf, BW; Wise, IJ | 1 |
Schimke, RN; Spiro, HR; Welch, JP | 1 |
Araki, S; Cowen, D; Rowland, LP; Thompson, HL; White, HH | 1 |
Dolman, CL; Dunn, HG; Perry, TL | 1 |
Gaitonde, MK; Gaull, G | 1 |
1 review(s) available for homocysteine and Intellectual Disability
Article | Year |
---|---|
[Hereditary anomalies of methionine metabolism in children].
Topics: Age Factors; Child; Flatfoot; Folic Acid; Homocysteine; Homocystine; Homocystinuria; Humans; Intellectual Disability; Kyphosis; Marfan Syndrome; Metabolism, Inborn Errors; Methionine; Scoliosis | 1972 |
16 other study(ies) available for homocysteine and Intellectual Disability
Article | Year |
---|---|
Correlation between cystathionine beta synthase gene polymorphisms, plasma homocysteine and idiopathic mental retardation in Indian individuals from Kolkata.
Topics: Adolescent; Adult; Case-Control Studies; Child; Child, Preschool; Cystathionine beta-Synthase; Female; Gene Frequency; Genotype; Haplotypes; Homocysteine; Humans; Intellectual Disability; Male; Polymorphism, Genetic; Sex Factors; White People; Young Adult | 2009 |
Treatment of extrapyramidal symptoms in a patient with homozygous homocystinuria.
Topics: Adult; Anticonvulsants; Clonazepam; Cystathionine beta-Synthase; Dystonia; Female; Homocysteine; Homocystinuria; Humans; Intellectual Disability | 2002 |
Hyperhomocysteinemia--case report.
Topics: Adult; Cerebrovascular Disorders; Exophthalmos; Female; Homocysteine; Homocystinuria; Humans; Hyperhomocysteinemia; Intellectual Disability | 2003 |
HOMOCYSTINURIA: A NEW INBORN ERROR OF METABOLISM ASSOCIATED WITH MENTAL DEFICIENCY.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Chromatography; Genetics, Medical; Homocysteine; Homocystinuria; Humans; Intellectual Disability; Kidney; Northern Ireland; Renal Aminoacidurias; Urologic Diseases | 1963 |
MENTAL RETARDATION AND THE INBORN ERRORS OF METABOLISM.
Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Arginine; Citrulline; Fructose; Galactosemias; Histidine; Homocysteine; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Renal Aminoacidurias; Vitamin B 6 Deficiency | 1964 |
A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Blood Chemical Analysis; Chromatography; Citrulline; Glycine; Histidine; Homocysteine; Humans; Hydroxyproline; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Proline; Proteins; Renal Aminoacidurias; Urine | 1964 |
HOMOCYSTINURIA: METABOLIC STUDIES ON 3 PATIENTS.
Topics: Amino Acid Metabolism, Inborn Errors; Blood; Child; Genetics, Medical; Homocysteine; Homocystine; Homocystinuria; Humans; Intellectual Disability; Metabolism; Methionine; Neomycin; Urine | 1965 |
Sulfur-containing amino acids in the plasma and urine of homocystinurics.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Chromatography, Paper; Homocysteine; Homocystine; Homocystinuria; Humans; Infant; Infant, Newborn; Intellectual Disability; Iodoacetates; Methionine; Sulfoxides; Sulfur; Ultraviolet Rays | 1967 |
Folate metabolism in humans.
Topics: Amino Acids; Cells, Cultured; Chemical Phenomena; Chemistry; Culture Media; Folic Acid; Folic Acid Deficiency; Fragile X Syndrome; Histidine; Homocysteine; Humans; Intellectual Disability; Lymphocytes; Sex Chromosome Aberrations; Tetrahydrofolates | 1984 |
Methylenetetrahydrofolate reductase deficiency: importance of early diagnosis.
Topics: Betaine; Child, Preschool; Diagnosis, Differential; Fatal Outcome; Fibroblasts; Folic Acid; Hematinics; Homocysteine; Homocystinuria; Homozygote; Humans; Infant; Intellectual Disability; Lipotropic Agents; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Oxidoreductases Acting on CH-NH Group Donors; Treatment Outcome | 2000 |
Mental retardation, megaloblastic anaemia, methylmalonic aciduria and abnormal homocysteine metabolism due to an error in vitamin B12 metabolism.
Topics: Amino Acid Isomerases; Amino Acids; Anemia, Macrocytic; Autopsy; Brain; Brain Chemistry; Cells, Cultured; Child; Culture Media; Fibroblasts; Homocysteine; Humans; Intellectual Disability; Liver; Lung; Lyases; Malonates; Metabolism, Inborn Errors; Methionine; Spleen; Vitamin B 12 | 1974 |
Homocystinuria due to cystathionine synthase deficiency.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Child; Female; Homocysteine; Homocystine; Homocystinuria; Humans; Hydro-Lyases; In Vitro Techniques; Intellectual Disability; Liver; Methionine | 1965 |
Schizophrenia in a patient with a defect in methionine metabolism.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Brain; Female; Homocysteine; Humans; Intellectual Disability; Methionine; Schizophrenia | 1965 |
Homocystinuria.
Topics: Amino Acid Metabolism, Inborn Errors; Brain; Child; Child, Preschool; Female; Homocysteine; Homocystine; Homocystinuria; Humans; Hydro-Lyases; In Vitro Techniques; Intellectual Disability; Intracranial Embolism and Thrombosis; Lens, Crystalline; Male; Methionine; Seizures | 1965 |
Homocystinuria. A recently discovered cause of mental defect and cerebrovascular thrombosis.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Animals; Blood; Blood Coagulation Disorders; Brain; Child; Child, Preschool; Cystine; Electroencephalography; Female; Homocysteine; Homocystine; Homocystinuria; Humans; In Vitro Techniques; Infant; Intellectual Disability; Intracranial Embolism and Thrombosis; Kidney Diseases; Male; Methionine; Taurine; Urine | 1966 |
Homocystinuria: an observation on the inheritance of cystathionine synthase deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Chromatography, Paper; Cystine; Homocysteine; Homocystinuria; Humans; Hydro-Lyases; Intellectual Disability; Lens, Crystalline; Male; Methionine; Middle Aged; Sulfur Isotopes | 1966 |