cystathionine has been researched along with Inborn Errors of Metabolism in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 8 (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 |
|---|---|
| Martin-DeLeon, PA | 1 |
| Endres, W; Wuttge, B | 1 |
| Athar, HS; Hasnain, SN | 1 |
| Harper, PS | 1 |
| Zakim, D | 1 |
| Brown, DA; Gaha, TJ; McLeay, AC; Smith, A; Wilcken, B | 1 |
| Frimpter, GW | 1 |
| Yoshida, T | 1 |
2 review(s) available for cystathionine and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Differential diagnosis and diseases due to enzyme changes.
Topics: Adrenal Hyperplasia, Congenital; Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Biological Transport, Active; Cell Membrane; Cystathionine; Diagnosis, Differential; Enzymes; Feedback; Galactosemias; Glycogen Storage Disease; Humans; Lesch-Nyhan Syndrome; Metabolism, Inborn Errors; Mucopolysaccharidoses; Mutation; Phenylketonurias; Tay-Sachs Disease; Vitamins | 1979 |
Biochemical foundations of preventive medicine: the study of abnormal enzymes.
Topics: Amino Acid Metabolism, Inborn Errors; Cystathionine; Cystathionine gamma-Lyase; Erythrocytes; Genes, Recessive; Genetic Variation; Glucosephosphate Dehydrogenase Deficiency; Glucuronosyltransferase; Glycogen Storage Disease Type I; Humans; Isoenzymes; Kinetics; Metabolism, Inborn Errors; Methylmalonic Acid; Orotic Acid; Purine-Pyrimidine Metabolism, Inborn Errors; Pyridoxine | 1974 |
6 other study(ies) available for cystathionine and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Occurrence of secondary cystathioninuria in children with inherited metabolic disorders, liver diseases, neoplasms, cystic fibrosis and celiac disease.
Topics: Adolescent; Age Factors; Bile Ducts; Celiac Disease; Child; Child, Preschool; Cystathionine; Cystic Fibrosis; Cytomegalovirus Infections; Humans; Infant; Liver Diseases; Metabolism, Inborn Errors; Neoplasms | 1978 |
Enzyme abnormalities in man and the role of their identification in preventive medicine.
Topics: Amino Acid Metabolism, Inborn Errors; Clinical Enzyme Tests; Cystathionine; Homogentisic Acid; Humans; Metabolism, Inborn Errors; Phenylalanine; Propionates | 1976 |
Inborn errors of metabolism-the relationship of clinical and biochemical abnormalities.
Topics: Cystathionine; Diseases in Twins; Glutamine; Homocystinuria; Humans; Infant, Newborn; Intellectual Disability; Lesch-Nyhan Syndrome; Metabolism, Inborn Errors; NADH, NADPH Oxidoreductases; Phenotype; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias | 1973 |
Screening for metabolic diseases in New South Wales.
Topics: Australia; Biological Assay; Chromatography, Paper; Cystathionine; Cystinuria; Female; Hartnup Disease; Homocystinuria; Humans; Infant, Newborn; Male; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Seasons | 1973 |
Recurrent urinary tract calculi possibly due to inherited cystathioninuria.
Topics: Adult; Aerospace Medicine; Chronic Disease; Cystathionine; Humans; Male; Metabolism, Inborn Errors; Pyridoxine; Urinary Calculi | 1973 |
[Vitamin B 6 dependency].
Topics: Child; Cystathionine; Female; Homocystinuria; Humans; Infant; Male; Metabolism, Inborn Errors; Pyridoxine; Xanthurenates | 1973 |