homocystine has been researched along with Metabolism, Inborn Errors in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (50.00) | 18.7374 |
| 1990's | 2 (20.00) | 18.2507 |
| 2000's | 3 (30.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hogan, K; Laxova, R; Rosenblatt, DS; Selzer, RR | 1 |
| Guthrie, R; Naylor, EW; Talbot, HW | 1 |
| Cooper, BA; Dilling, LA; Haworth, JC; Lue-Shing, H; Rosenblatt, DS; Seargeant, LE; Surtees, RA | 1 |
| Andersson, HC; Shapira, E | 1 |
| Beatty, S; Lloyd, IC; Patton, N; Wraith, JE | 1 |
| Amirthalakshmi, S; Ramakrishnan, S; Sulochana, KN; Tamilselvi, R; Vasanthi, SB | 1 |
| Enzenauer, J; Matz, D; Menne, F | 1 |
| Sviatkina, OB; Vel'tishchev, IuE | 1 |
| Abeles, RH; Dreyfus, PM; Levy, HL; Mudd, SH; Schulman, JD | 1 |
| Abeles, RH; Jennedy, JP; Levy, HL; Mudd, SH | 1 |
1 review(s) available for homocystine and Metabolism, Inborn Errors
| 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 |
9 other study(ies) available for homocystine and Metabolism, Inborn Errors
| Article | Year |
|---|---|
Adverse effect of nitrous oxide in a child with 5,10-methylenetetrahydrofolate reductase deficiency.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; 5,10-Methylenetetrahydrofolate Reductase (FADH2); Anesthetics, Inhalation; Cells, Cultured; DNA Mutational Analysis; Fatal Outcome; Fibroblasts; Folic Acid; Genes, Recessive; Homocysteine; Homocystine; Humans; Hyperhomocysteinemia; Infant; Male; Metabolism, Inborn Errors; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Nitrous Oxide; Oxidoreductases; Point Mutation; Polymorphism, Genetic; RNA | 2003 |
Neonatal urine screening for metabolic disease with auxotrophic strains of Bacillus subtilis.
Topics: Bacillus subtilis; Biological Assay; Homocystine; Humans; Infant, Newborn; Lysine; Metabolism, Inborn Errors; Mutation; Uracil | 1982 |
Symptomatic and asymptomatic methylenetetrahydrofolate reductase deficiency in two adult brothers.
Topics: Adult; Betaine; Enzyme Stability; Folic Acid; Homocystine; Humans; Male; Metabolism, Inborn Errors; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Nervous System Diseases; Oxidoreductases Acting on CH-NH Group Donors; Paraparesis, Tropical Spastic | 1993 |
Biochemical and clinical response to hydroxocobalamin versus cyanocobalamin treatment in patients with methylmalonic acidemia and homocystinuria (cblC).
Topics: Child; Child, Preschool; Female; Growth; Homocystine; Homocystinuria; Humans; Hydroxocobalamin; Infant; Male; Metabolism, Inborn Errors; Methylmalonic Acid; Vitamin B 12 | 1998 |
Optic atrophy in association with cobalamin C (cblC) disease.
Topics: Age of Onset; Child, Preschool; Consanguinity; Female; Follow-Up Studies; Homocystine; Homocystinuria; Humans; Metabolism, Inborn Errors; Methylmalonic Acid; Optic Atrophy; Vitamin B 12 | 2000 |
Homocystinuria with congenital/developmental cataract.
Topics: Adult; Cataract; Child; Chromatography, Paper; Female; Homocystine; Homocystinuria; Humans; Male; Mass Screening; Metabolism, Inborn Errors; Methionine; Pyridoxine | 2000 |
[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 |
A derangement in B12 metabolism associated with homocystinemia, cystathioninemia, hypomethioninemia and methylmalonic aciduria.
Topics: Acidosis; Amino Acids; Aminobutyrates; Brain; Chromatography, Paper; Fibroblasts; Homocystine; Humans; Hydro-Lyases; Infant, Newborn; Infant, Newborn, Diseases; Isomerases; Kidney; Liver; Male; Malonates; Metabolism, Inborn Errors; Methionine; Transferases; Vitamin B 12; Vitamin B 12 Deficiency | 1970 |
A derangement in B 12 metabolism leading to homocystinemia, cystathioninemia and methylmalonic aciduria.
Topics: Amino Acid Metabolism, Inborn Errors; Aminobutyrates; Brain; Homocysteine; Homocystine; Homocystinuria; Humans; Infant; Kidney; Liver; Male; Malonates; Metabolism, Inborn Errors; Methionine; Sulfides; Transferases; Vitamin B 12 | 1969 |