tryptophan has been researched along with Carbohydrate Metabolism, Inborn Error in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (85.71) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (14.29) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| De Vivo, DC; Fujii, T; Ho, YY; Ito, M; Kudo, T; Miyajima, T; Shirasaka, Y; Tsang, PT; Wang, D; Wong, HY | 1 |
| Francois, J | 1 |
| Eriksson, O; Hultberg, B; Ockerman, PA | 1 |
| Collipp, PJ; Maddaiah, VT; Sharma, RK; Thomas, JT | 1 |
| Tabolin, VA | 1 |
| Alpers, DH; Thier, SO | 1 |
| Gibbs, DA; Watts, RW | 1 |
2 review(s) available for tryptophan and Carbohydrate Metabolism, Inborn Error
| Article | Year |
|---|---|
Hereditary chorioretinal degeneration and metabolic disturbances.
Topics: Abetalipoproteinemia; Amino Acid Metabolism, Inborn Errors; Animals; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Cystinosis; Cystinuria; Female; Growth Disorders; Humans; Lipid Metabolism, Inborn Errors; Lipids; Lipoproteins; Metabolism, Inborn Errors; Mice; Mucopolysaccharidoses; Rabbits; Rats; Refsum Disease; Retinal Degeneration; Retinal Pigments; Tryptophan | 1968 |
Disorders of intestinal transport of amino acids.
Topics: Amino Acids; Arginine; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Fructose; Galactosemias; Genes, Recessive; Glycine; Hartnup Disease; Humans; Intestinal Absorption; Lysine; Methionine; Phenylketonurias; Proline; Renal Tubular Transport, Inborn Errors; Tryptophan | 1969 |
5 other study(ies) available for tryptophan and Carbohydrate Metabolism, Inborn Error
| Article | Year |
|---|---|
Three Japanese patients with glucose transporter type 1 deficiency syndrome.
Topics: 3-Hydroxybutyric Acid; Adult; Arginine; Brain Diseases, Metabolic, Inborn; Brain Mapping; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Glucose Transporter Type 1; Humans; Japan; Male; Methionine; Mutation, Missense; Positron-Emission Tomography; Threonine; Tryptophan | 2007 |
Urinary amino acids in storage disorders: mucopolysaccharidosis, Gaucher's disease and metachromatic leucodystrophy.
Topics: Adolescent; Adult; Amino Acids; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Diffuse Cerebral Sclerosis of Schilder; Female; Gaucher Disease; Glycolipids; Glycoproteins; Glycosaminoglycans; Humans; Intellectual Disability; Lysosomes; Male; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa; Serine; Threonine; Tryptophan | 1969 |
Abnormal glucose metabolism in diastrophic dwarfism.
Topics: Administration, Oral; Blood Glucose; Carbohydrate Metabolism, Inborn Errors; Child; Cholesterol; Glucose; Glucose Tolerance Test; Glycosaminoglycans; Growth Hormone; Humans; Male; Radiography; Syndrome; Triglycerides; Tryptophan | 1972 |
[Metabolic disorders, their early diagnosis and therapy in newborn infants].
Topics: Adrenal Hyperplasia, Congenital; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Cystic Fibrosis; Fanconi Syndrome; Humans; Hyperbilirubinemia, Hereditary; Immunologic Deficiency Syndromes; Infant; Infant, Newborn; Jaundice, Neonatal; Malabsorption Syndromes; Neurologic Manifestations; Phenylketonurias; Tryptophan | 1973 |
The action of pyridoxine in primary hyperoxaluria.
Topics: Carbohydrate Metabolism, Inborn Errors; Glyoxylates; Humans; Kynurenic Acid; Kynurenine; ortho-Aminobenzoates; Oxalates; Pyridoxine; Tryptophan | 1969 |