tryptophan has been researched along with Inborn Errors of Metabolism in 36 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 33 (91.67) | 18.7374 |
1990's | 2 (5.56) | 18.2507 |
2000's | 1 (2.78) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
GREGORATOS, G; MOSER, RH; VENNES, GJ | 1 |
DRUMMOND, KN; GOOD, RA; MICHAEL, AF; ULSTROM, RA | 1 |
JEROME, H | 1 |
DRUCKMAN, R; FRENCH, JH; GRUETER, BB; O'BRIEN, D | 1 |
BICKEL, H | 1 |
Albahri, Z; Marklová, E; Nozicková, M | 1 |
Brown, RR; Johnson, AM; Price, JM; Yess, N | 1 |
Shideler, CE | 1 |
Brown, RR; Fischer, MH | 1 |
Goodman, SI; Markey, SP | 1 |
Batshaw, ML; Heyes, MP; Hopkins, K; McLaughlin, BA; Oster-Granite, ML; Robinson, MB | 1 |
Forman, P; Justice, P; Tabahoff, B; Wong, PW | 1 |
Brown, RR; Leklem, JE | 1 |
Gilka, L | 1 |
Anegawa, NJ; Batshaw, ML; Djali, S; Gorry, E; Heyes, MP; Mellits, ED; Robinson, MB | 1 |
Francois, J | 1 |
Attal, C; Boisse, J; Charpentier, C; Lévy, H; Mozziconacci, P | 1 |
Brown, RR; Price, JM; Yess, N | 1 |
Chiancone, FM; Mainardi, L; Tenconi, LT | 1 |
Mandell, AJ; Spooner, CE | 1 |
Grimm, U; Jährig, K; Knapp, A; Lubs, H; Schlenzka, K; Schulz, M | 1 |
Barthélémy, JP; Bousquet, B; Civatte, J; Dreux, C; Larregue, M | 1 |
Reed, WB | 1 |
Hsia, DY | 1 |
Feist, D; Kochen, W | 1 |
Binazzi, M | 1 |
Arakawa, T; Higashi, O; Ohara, K; Tamura, T; Tanno, K | 1 |
Buss, EG; Clagett, CO; Farrell, HM; Mallette, MF | 1 |
Grosser, V; Hinkel, GK; Kintzel, HW; Knapp, A | 1 |
Knapp, A | 2 |
Arakawa, T; Nakagawa, H; Tada, K; Yokoyama, Y | 1 |
Charpentier, C; Leluc, R; Lemonnier, A | 2 |
Attal, C; Boisse, J; Leluc, R; Mozziconacci, P | 1 |
8 review(s) available for tryptophan and Inborn Errors of Metabolism
Article | Year |
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[THE BIOCHEMICAL EFFECTS OF CERTAIN CHROMOSOMES].
Topics: Alkaline Phosphatase; Chromosome Aberrations; Chromosomes; Electrophoresis; Glucosephosphate Dehydrogenase; Hemoglobins; Humans; Hydroxyindoleacetic Acid; Indoleacetic Acids; Metabolism; Metabolism, Inborn Errors; Proteins; Transferases; Trisomy; Tryptophan; Urine | 1964 |
Vitamin B6: an overview.
Topics: Adult; Animals; Chemical Phenomena; Chemistry; Child; Female; Humans; Infant; Metabolism, Inborn Errors; Pyridoxal Phosphate; Pyridoxine; Rats; Transaminases; Tryptophan; Vitamin B 6 Deficiency | 1983 |
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 |
Testing the functional capacity of the tryptophan-niacin pathway in man by analysis of urinary metabolites.
Topics: Adult; Amides; Amines; Chromatography, Ion Exchange; Equipment and Supplies; Female; Hormones; Humans; Indican; Ion Exchange Resins; Kynurenic Acid; Male; Metabolism, Inborn Errors; Methods; Niacinamide; Nicotinic Acids; Phenols; Pregnancy; Pyridoxine; Spectrophotometry; Tryptophan; Vitamins; Xanthurenates | 1965 |
Psychochemical research studies in man.
Topics: Animals; Behavior; Bipolar Disorder; Brain; Brain Chemistry; Depression; Dihydroxyphenylalanine; Hallucinogens; Hartnup Disease; Humans; Imipramine; Metabolism, Inborn Errors; Models, Neurological; Neurons; Neurotransmitter Agents; Norepinephrine; Phenylketonurias; Psychopharmacology; Sleep, REM; Tryptophan | 1968 |
Metabolic changes in acrodermatitis enteropathica.
Topics: Acrodermatitis; Amino Acid Metabolism, Inborn Errors; Celiac Disease; Diarrhea, Infantile; Fatty Acids, Unsaturated; Humans; Immunity; Immunologic Deficiency Syndromes; Infant; Infant Nutritional Physiological Phenomena; Iodoquinol; Male; Metabolism, Inborn Errors; Nutrition Disorders; Tryptophan | 1974 |
The genetics of the photodermatoses.
Topics: Adolescent; DNA Repair; DNA Replication; Ethnicity; Female; Genes, Dominant; Genes, Recessive; Humans; Indians, North American; Lupus Erythematosus, Systemic; Male; Metabolism, Inborn Errors; Middle Aged; Photosensitivity Disorders; Porphyrias; Porphyrins; Renal Aminoacidurias; Skin Diseases; Tryptophan; Xeroderma Pigmentosum | 1971 |
Biochemical factors in mental retardation.
Topics: 5-Hydroxytryptophan; Animals; Brain Chemistry; Diet Therapy; Female; Guinea Pigs; Haplorhini; Humans; Infant; Intellectual Disability; Intelligence Tests; Male; Metabolism, Inborn Errors; Monoamine Oxidase; Phenylalanine; Phenylketonurias; Rats; Serotonin; Tryptophan; Tyrosine | 1967 |
28 other study(ies) available for tryptophan and Inborn Errors of Metabolism
Article | Year |
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CONGENITAL INCLUSION BODY HEMOLYTIC ANEMIA ASSOCIATED WITH EPILEPSY AND DISORDERED PYRIDOXINE METABOLISM.
Topics: Adolescent; Anemia; Anemia, Hemolytic, Congenital; Bile Pigments; Child; Epilepsy; Erythrocytes; Glutathione; Hemoglobins; Hemosiderosis; Humans; Inclusion Bodies; Kidney Diseases; Liver Diseases; Metabolism; Metabolism, Inborn Errors; Necrosis; Pyridoxine; Tryptophan | 1964 |
THE BLUE DIAPER SYNDROME: FAMILIAL HYPERCALCEMIA WITH NEPHROCALCINOSIS AND INDICANURIA; A NEW FAMILIAL DISEASE, WITH DEFINITION OF THE METABOLIC ABNORMALITY.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Blood Protein Electrophoresis; Chromatography; Electrophoresis; Eye Abnormalities; Humans; Hypercalcemia; Indican; Indoles; Intestinal Absorption; Kidney Diseases; Kidney Function Tests; Lipid Metabolism; Metabolism, Inborn Errors; Nephrocalcinosis; Pathology; Radiography; Spectrophotometry; Tryptophan; Urine; Vitamins | 1964 |
PYRIDOXINE AND INFANTILE MYOCLONIC SEIZURES.
Topics: Amino Acids; Drug Therapy; Electroencephalography; Epilepsies, Myoclonic; Humans; Infant; Kynurenic Acid; Metabolism, Inborn Errors; Myoclonus; Phenytoin; Pyridoxine; Seizures; Spasms, Infantile; Tryptophan; Urine; Xanthurenates | 1965 |
[THE "BLUE DIAPER" SYNDROME].
Topics: Amino Acid Metabolism, Inborn Errors; Eye Abnormalities; Humans; Hypercalcemia; Indoles; Infant; Intestinal Absorption; Kidney Diseases; Metabolism, Inborn Errors; Tryptophan | 1965 |
HPLC profiling of Trp-related metabolites in humans.
Topics: Adolescent; Adult; Aged; Case-Control Studies; Child; Child, Preschool; Chromatography, High Pressure Liquid; Humans; Infant; Metabolism, Inborn Errors; Middle Aged; Photosensitivity Disorders; Skin Diseases; Tryptophan | 2003 |
Tryptophan metabolism. A hitherto unreported abnormality occurring in a family.
Topics: Chlorotrianisene; Electroencephalography; Female; Humans; Injections, Intramuscular; Kynurenine; Male; Metabolism, Inborn Errors; Pyridoxine; Scleroderma, Systemic; Tryptophan | 1967 |
Tryptophan and lysine metabolism in alpha-aminoadipic aciduria.
Topics: 2-Aminoadipic Acid; Amino Acids, Dicarboxylic; Child; Humans; Intellectual Disability; Lysine; Male; Metabolism, Inborn Errors; Tryptophan | 1980 |
Diagnosis of organic acidemias by gas chromatography--mass spectrometry.
Topics: Acid-Base Imbalance; Gas Chromatography-Mass Spectrometry; Humans; Isoleucine; Leucine; Lysine; Metabolism, Inborn Errors; Tryptophan; Valine | 1981 |
Evidence of excitotoxicity in the brain of the ornithine carbamoyltransferase deficient sparse fur mouse.
Topics: Ammonia; Animals; Brain Damage, Chronic; Disease Models, Animal; Glutamine; Hair; Metabolism, Inborn Errors; Mice; Mice, Inbred Strains; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Quinolinic Acid; Tryptophan | 1995 |
A defect in tryptophan metabolism.
Topics: Cerebellar Ataxia; Child; Chromatography, Paper; Drug Eruptions; Humans; Kynurenic Acid; Kynurenine; Male; Metabolic Clearance Rate; Metabolism, Inborn Errors; Nicotinic Acids; Photosensitivity Disorders; Tryptophan; Xanthurenates | 1976 |
Abnormal tryptophan metabolism in a family with a history of bladder cancer.
Topics: Aged; Female; Humans; Kynurenine; Male; Metabolism, Inborn Errors; Middle Aged; Pyridoxine; Tryptophan; Urinary Bladder Neoplasms | 1976 |
Schizophrenia, a disorder of tryptophan metabolism.
Topics: Catecholamines; Diet; Hallucinogens; Humans; Indoles; Metabolism, Inborn Errors; Monoamine Oxidase; Schizophrenia; Tryptophan | 1975 |
Quinolinate in brain and cerebrospinal fluid in rat models of congenital hyperammonemia.
Topics: Acetates; Ammonia; Animals; Brain; Disease Models, Animal; Hydroxyindoleacetic Acid; Male; Metabolism, Inborn Errors; Quinolinic Acid; Rats; Rats, Sprague-Dawley; Tryptophan; Urease | 1992 |
[Tryptophan tolerance test in children].
Topics: Adolescent; Child; Child, Preschool; Down Syndrome; Hartnup Disease; Humans; Infant; Metabolism, Inborn Errors; Phenylketonurias; Seizures; Tryptophan; Vitamin B Deficiency | 1964 |
[Tryptophan metabolism in screening metabolic diseases of the newborn].
Topics: Amino Acid Metabolism, Inborn Errors; Evaluation Studies as Topic; Female; Humans; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature; Liver; Mass Screening; Metabolism, Inborn Errors; Methods; Niacinamide; Pregnancy; Tryptophan; Tryptophan Oxygenase | 1973 |
[Tryptophan metabolism studies in two siblings with oligophrenia and convulsions].
Topics: Child, Preschool; Humans; Infant; Intellectual Disability; Male; Metabolism, Inborn Errors; Seizures; Tryptophan | 1972 |
[Pellagroid syndrome with vitamin B6 deficiency. Biological and clinical study of a case].
Topics: Amino Acids; Cystine; Humans; Indoleacetic Acids; Liver Cirrhosis; Male; Metabolism, Inborn Errors; Methionine; Middle Aged; Pellagra; Serotonin; Sulfur; Taurine; Tryptophan; Vitamin B 6 Deficiency; Xanthurenates | 1972 |
[Studies of tryptophan metabolism in pyridoxin-dependent convulsions].
Topics: Child, Preschool; Epilepsy, Tonic-Clonic; Humans; Metabolism, Inborn Errors; Pyridoxine; Tryptophan; Vitamin B 6 Deficiency | 1971 |
[Pathogenesis of photodermatosis].
Topics: Dermatitis; Humans; Lupus Erythematosus, Systemic; Metabolism, Inborn Errors; Nicotinic Acids; Pellagra; Photosensitivity Disorders; Porphyrias; Skin Diseases; Tryptophan | 1972 |
Formiminotransferase deficiency syndrome associated with megaloblastic anemia responsive to pyridoxine or folic acid.
Topics: Anemia, Macrocytic; Blood Cell Count; Bone Marrow Examination; Cerebral Ventriculography; Erythrocytes; FIGLU Test; Folic Acid; Humans; Infant; Infusions, Parenteral; Injections, Intramuscular; Liver; Male; Metabolism, Inborn Errors; Pyridoxal Phosphate; Tetrahydrofolate Dehydrogenase; Transferases; Tryptophan | 1968 |
The nature of the biochemical lesion in avian renal riboflavinuria. 3. The isolation and characterization of the riboflavin-binding protein from egg albumen.
Topics: Amino Acids; Animals; Buffers; Carbohydrates; Cellulose; Chemical Phenomena; Chemistry; Chickens; Chromatography, Ion Exchange; Cold Temperature; Drug Stability; Electrophoresis; Female; Galactose; Genes, Recessive; Glucosamine; Homozygote; Hydrogen Peroxide; Hydrogen-Ion Concentration; Mannose; Metabolism, Inborn Errors; Methods; Molecular Weight; Mutation; Osmolar Concentration; Ovalbumin; Poultry Diseases; Protein Binding; Proteins; Riboflavin; Sulfides; Time Factors; Tryptophan; Ultracentrifugation | 1969 |
[Vitamin-B6-dependent pediatric diseases. Hereditary pyridoxine-dependent spasms in newborns and xanthurenuria in parents].
Topics: Adult; Female; Humans; Infant, Newborn; Infant, Newborn, Diseases; Metabolism, Inborn Errors; Pregnancy; Pyridoxine; Seizures; Tryptophan; Vitamin B 6 Deficiency; Xanthurenates | 1970 |
[Genetic disorders in tryptophan metabolism].
Topics: Hartnup Disease; Humans; Kynurenine; Metabolism, Inborn Errors; Tryptophan | 1967 |
Vitamin B6 dependent xanthurenic aciduria (the second report).
Topics: Acids; Amino Acids; Aspartate Aminotransferases; Child, Preschool; Erythrocytes; Female; Humans; Hydrolases; Intellectual Disability; Liver; Metabolism, Inborn Errors; Pyridoxine; Tryptophan; Xanthurenates | 1968 |
[Biochemical and analytical bases of exploration of metabolism of tryptophan].
Topics: Humans; Indoles; Metabolism, Inborn Errors; Tryptophan | 1964 |
[Biochemical and analytical bases of the exploration of phenylalanine metabolism].
Topics: Humans; Intellectual Disability; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Tryptophan; Tyrosine | 1964 |
["Borderline" forms of phenylketonuria].
Topics: Adolescent; Child, Preschool; Humans; Infant; Intellectual Disability; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Serotonin; Tryptophan | 1964 |
[Recent studies on a genetic disorder of tryptophan metabolism and its relations to vitamin B6].
Topics: Asthma; Eczema; Humans; Kynurenic Acid; Leg Ulcer; Metabolism, Inborn Errors; Pyridoxine; Tryptophan; Urticaria; Xanthurenates | 1965 |