taurine has been researched along with Metabolic Diseases in 8 studies
Metabolic Diseases: Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed)
Excerpt | Relevance | Reference |
---|---|---|
"Cystathionine was absent in the cerebrum of a patient with homocystinuria." | 7.64 | HOMOCYSTINURIA: ABSENCE OF CYSTATHIONINE IN THE BRAIN. ( GERRITSEN, T; WAISMAN, HA, 1964) |
"Cystathionine was absent in the cerebrum of a patient with homocystinuria." | 3.64 | HOMOCYSTINURIA: ABSENCE OF CYSTATHIONINE IN THE BRAIN. ( GERRITSEN, T; WAISMAN, HA, 1964) |
"Maternal obesity is associated with obesity and metabolic disorders in offspring." | 1.56 | Long-term effects of a maternal high-fat: high-fructose diet on offspring growth and metabolism and impact of maternal taurine supplementation. ( Gray, C; Li, M; Patel, R; Reynolds, CM; Sloboda, DM; Vickers, MH, 2020) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 5 (62.50) | 18.7374 |
1990's | 2 (25.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (12.50) | 2.80 |
Authors | Studies |
---|---|
Li, M | 1 |
Reynolds, CM | 1 |
Gray, C | 1 |
Patel, R | 1 |
Sloboda, DM | 1 |
Vickers, MH | 1 |
GERRITSEN, T | 1 |
WAISMAN, HA | 1 |
Riva, E | 1 |
Borzani, M | 1 |
Motta, G | 1 |
Giovannini, M | 1 |
Caspary, WF | 1 |
Libert, R | 1 |
Hermans, D | 1 |
Draye, JP | 1 |
Van Hoof, F | 1 |
Sokal, E | 1 |
de Hoffmann, E | 1 |
Jellum, E | 1 |
Thorsrud, AK | 1 |
Time, E | 1 |
Valman, HB | 1 |
Oberholzer, VG | 1 |
Palmer, T | 1 |
8 other studies available for taurine and Metabolic Diseases
Article | Year |
---|---|
Long-term effects of a maternal high-fat: high-fructose diet on offspring growth and metabolism and impact of maternal taurine supplementation.
Topics: Animals; Animals, Newborn; Diet, High-Fat; Dietary Supplements; Female; Fructose; Male; Metabolic Di | 2020 |
HOMOCYSTINURIA: ABSENCE OF CYSTATHIONINE IN THE BRAIN.
Topics: Amino Acids; Brain; Child; Chromatography; Cystathionine; Cystathionine beta-Synthase; Cystine; Homo | 1964 |
[Changes of serum ammonium in various pediatric diseases in relation to the treatment with anti-ammonemic drugs].
Topics: Ammonia; Arginine; Carboxylic Acids; Child, Preschool; Citrates; Female; Humans; Infant; Male; Metab | 1976 |
[Acquired hyperoxaluria and nephrolithiasis in gastrointestinal diseases ("enteral" hyperoxaluria)].
Topics: Carbon Radioisotopes; Gastrointestinal Diseases; Glycine; Glyoxylates; Humans; Intestinal Absorption | 1975 |
Bile acids and conjugates identified in metabolic disorders by fast atom bombardment and tandem mass spectrometry.
Topics: Adrenoleukodystrophy; Bile Acids and Salts; Glycine; Humans; Hydroxylation; Mass Spectrometry; Metab | 1991 |
Capillary electrophoresis for diagnosis and studies of human disease, particularly metabolic disorders.
Topics: Biopsy; Chromatography, High Pressure Liquid; Cystinuria; Electrophoresis; Homocystinuria; Humans; M | 1991 |
[Pathogenesis and therapy of hyperoxaluria].
Topics: Humans; Ileum; Intestinal Diseases; Kidney Calculi; Metabolic Diseases; Oxalates; Taurine | 1973 |
Hyperoxaluria after resection of ileum in childhood.
Topics: Adolescent; Age Factors; Bile; Child; Child, Preschool; Glycine; Humans; Ileum; Infant; Infant, Newb | 1974 |