homocystine has been researched along with Intellectual Disability in 20 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 20 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| BRENTON, DP; CUSWORTH, DC; GAULL, GE | 1 |
| Smith, SW | 1 |
| Hansen, S; MacDougall, L; Perry, TL; Warrington, PD | 1 |
| Greer, M; Williams, CM | 1 |
| Arakawa, T; Hirono, H; Tada, K; Yoshida, T | 1 |
| Enzenauer, J; Matz, D; Menne, F | 1 |
| Crawford, LE; Hansen, S; Love, DL; Perry, TL; Tischler, B | 1 |
| Sviatkina, OB; Vel'tishchev, IuE | 1 |
| Gröbe, H | 1 |
| Gebala, A; Kozlowska, T | 1 |
| Carson, NA | 1 |
| Charpentier, C; Lemonnier, A; Moatti, N; Pousset, JL | 1 |
| Falk, W | 1 |
| Anders, PW; Curtius, HC; Martenet, AC | 1 |
| Boisse, J | 1 |
| Mudd, SH; Uhlendorf, BW | 1 |
| Harper, JR; Parkinson, MS | 1 |
| Araki, S; Cowen, D; Rowland, LP; Thompson, HL; White, HH | 1 |
| Dolman, CL; Dunn, HG; Perry, TL | 1 |
1 review(s) available for homocystine 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 |
19 other study(ies) available for homocystine and Intellectual Disability
| Article | Year |
|---|---|
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 |
Roentgen findings in homocystinuria.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Female; Homocystine; Homocystinuria; Humans; Intellectual Disability; Male; Marfan Syndrome; Osteoporosis; Radiography; Spinal Diseases; Thoracic Diseases | 1967 |
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 |
Diagnosis of homocystinuria by gas chromatography.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Gas; Chromatography, Ion Exchange; Fluoroacetates; Homocystine; Homocystinuria; Humans; Intellectual Disability; Marfan Syndrome; Quaternary Ammonium Compounds | 1967 |
Homocystinuria: amino acid pattern of the liver.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Autoanalysis; Child, Preschool; Cystine; Homocystine; Homocystinuria; Humans; Hydro-Lyases; Intellectual Disability; Liver; Male; Methionine | 1967 |
[Diagnosis and therapy of 6 hereditary, to mental-deficiency-leading, metabolic disorders. 2].
Topics: Acute Disease; Diagnosis, Differential; Galactose; Galactosemias; Germany, West; Histidine; Homocystine; Homocystinuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Methionine; Phosphotransferases | 1976 |
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; Cystine; Diet Therapy; Female; Follow-Up Studies; Homocystine; Homocystinuria; Humans; Intellectual Disability; Male; Methionine; Pyridoxine; Thrombosis | 1968 |
[Homocystinuria: clinical picture, therapy and results in 8 patients].
Topics: Body Weight; Child; Child, Preschool; Cystine; Dietary Proteins; Female; Hair; Homocystine; Homocystinuria; Humans; Infant; Intellectual Disability; Methionine; Pyridoxine | 1973 |
The role of homocystinuria in the etiopathogenesis of children's mental deficiency.
Topics: Adolescent; Age Factors; Amino Acids; Child, Preschool; False Positive Reactions; Homocystine; Homocystinuria; Humans; Intellectual Disability; Methionine; Methods; Vision Disorders | 1973 |
Chemical pathology of amino acid diseases.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Chemical Phenomena; Chemistry; Child; Child, Preschool; Female; Homocystine; Humans; Hypoglycemia; Infant; Intellectual Disability; Leucine; Male; Maple Syrup Urine Disease; Methionine; Pyridoxine; Valine | 1968 |
[Isolation and identification of a new urinary oxydative metabolite of homocystine].
Topics: Aminobutyrates; Ammonia; Chemical Phenomena; Chemistry; Child; Chromatography, Ion Exchange; Chromatography, Paper; Drug Stability; Electrophoresis; Formates; Homocystine; Humans; Intellectual Disability; Male; Mass Spectrometry; Oxidation-Reduction; Paper; Sulfones | 1971 |
[Abortive form of homocystinuria].
Topics: Adolescent; Child, Preschool; Chromatography; Chromatography, Paper; Diagnosis, Differential; Eye Diseases; Female; Follow-Up Studies; Homocystine; Homocystinuria; Humans; Intellectual Disability; Marfan Syndrome; Methionine; Myopia; Vitreous Body | 1970 |
[Determination of free amino acids in aqueous humor of homocystinuria patients and in control subjects].
Topics: Aged; Amino Acid Metabolism, Inborn Errors; Amino Acids; Aqueous Humor; Autoanalysis; Child; Homocystine; Homocystinuria; Humans; Intellectual Disability; Marfan Syndrome; Methionine; Middle Aged | 1968 |
[Attempted clinical orientation in the diagnosis of amino acid metabolism disorders. I. Urinary symptoms, neuropsychic symptoms and ocular symtpoms].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Eye Diseases; Homocystine; Humans; Intellectual Disability; Metabolic Diseases; Muscular Diseases; Phenylketonurias; Renal Aminoacidurias; Seizures; Urine | 1968 |
Cystathionine synthase in tissue culture derived from human skin: enzyme defect in homocystinuria.
Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Culture Techniques; Fibroblasts; Homocystine; Homocystinuria; Humans; Hydro-Lyases; Intellectual Disability; Methionine; Skin; Transferases | 1968 |
Therapeutic problems of adolescent homocystinuria.
Topics: Child; Diet Therapy; Homocystine; Homocystinuria; Humans; Intellectual Disability; Male; Methionine; Thromboembolism | 1969 |
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 |
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 |