tryptophan and Metabolism, Inborn Errors

tryptophan has been researched along with Metabolism, Inborn Errors in 36 studies

Research

Studies (36)

TimeframeStudies, this research(%)All Research%
pre-199033 (91.67)18.7374
1990's2 (5.56)18.2507
2000's1 (2.78)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
GREGORATOS, G; MOSER, RH; VENNES, GJ1
DRUMMOND, KN; GOOD, RA; MICHAEL, AF; ULSTROM, RA1
JEROME, H1
DRUCKMAN, R; FRENCH, JH; GRUETER, BB; O'BRIEN, D1
BICKEL, H1
Albahri, Z; Marklová, E; Nozicková, M1
Brown, RR; Johnson, AM; Price, JM; Yess, N1
Shideler, CE1
Brown, RR; Fischer, MH1
Goodman, SI; Markey, SP1
Batshaw, ML; Heyes, MP; Hopkins, K; McLaughlin, BA; Oster-Granite, ML; Robinson, MB1
Forman, P; Justice, P; Tabahoff, B; Wong, PW1
Brown, RR; Leklem, JE1
Gilka, L1
Anegawa, NJ; Batshaw, ML; Djali, S; Gorry, E; Heyes, MP; Mellits, ED; Robinson, MB1
Francois, J1
Attal, C; Boisse, J; Charpentier, C; Lévy, H; Mozziconacci, P1
Brown, RR; Price, JM; Yess, N1
Chiancone, FM; Mainardi, L; Tenconi, LT1
Mandell, AJ; Spooner, CE1
Grimm, U; Jährig, K; Knapp, A; Lubs, H; Schlenzka, K; Schulz, M1
Barthélémy, JP; Bousquet, B; Civatte, J; Dreux, C; Larregue, M1
Reed, WB1
Hsia, DY1
Feist, D; Kochen, W1
Binazzi, M1
Arakawa, T; Higashi, O; Ohara, K; Tamura, T; Tanno, K1
Buss, EG; Clagett, CO; Farrell, HM; Mallette, MF1
Grosser, V; Hinkel, GK; Kintzel, HW; Knapp, A1
Knapp, A2
Arakawa, T; Nakagawa, H; Tada, K; Yokoyama, Y1
Charpentier, C; Leluc, R; Lemonnier, A2
Attal, C; Boisse, J; Leluc, R; Mozziconacci, P1

Reviews

8 review(s) available for tryptophan and Metabolism, Inborn Errors

ArticleYear
[THE BIOCHEMICAL EFFECTS OF CERTAIN CHROMOSOMES].
    Annales de genetique, 1964, Volume: 7

    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.
    The American journal of medical technology, 1983, Volume: 49, Issue:1

    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.
    International ophthalmology clinics, 1968,Winter, Volume: 8, Issue:4

    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.
    Advances in metabolic disorders, 1965, Volume: 2

    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.
    Science (New York, N.Y.), 1968, Dec-27, Volume: 162, Issue:3861

    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.
    Nutrition reviews, 1974, Volume: 32, Issue:6

    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.
    Birth defects original article series, 1971, Volume: 7, Issue:8

    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.
    Proceedings of the annual meeting of the American Psychopathological Association, 1967, Volume: 56

    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

Other Studies

28 other study(ies) available for tryptophan and Metabolism, Inborn Errors

ArticleYear
CONGENITAL INCLUSION BODY HEMOLYTIC ANEMIA ASSOCIATED WITH EPILEPSY AND DISORDERED PYRIDOXINE METABOLISM.
    Blood, 1964, Volume: 24

    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.
    The American journal of medicine, 1964, Volume: 37

    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.
    Neurology, 1965, Volume: 15

    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].
    Deutsche medizinische Wochenschrift (1946), 1965, May-14, Volume: 90

    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.
    Advances in experimental medicine and biology, 2003, Volume: 527

    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.
    Archives of dermatology, 1967, Volume: 95, Issue:5

    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.
    American journal of medical genetics, 1980, Volume: 5, Issue:1

    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.
    Laboratory and research methods in biology and medicine, 1981, Volume: 6

    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.
    Brain research. Developmental brain research, 1995, Dec-21, Volume: 90, Issue:1-2

    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.
    Pediatric research, 1976, Volume: 10, Issue:8

    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.
    Journal of the National Cancer Institute, 1976, Volume: 56, Issue:6

    Topics: Aged; Female; Humans; Kynurenine; Male; Metabolism, Inborn Errors; Middle Aged; Pyridoxine; Tryptophan; Urinary Bladder Neoplasms

1976
Schizophrenia, a disorder of tryptophan metabolism.
    Acta psychiatrica Scandinavica. Supplementum, 1975, Volume: 258

    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.
    Pediatric research, 1992, Volume: 32, Issue:4

    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].
    Annales de pediatrie, 1964, Mar-02, Volume: 11, Issue:3

    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].
    Acta vitaminologica et enzymologica, 1973, Volume: 27, Issue:5

    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].
    Das Deutsche Gesundheitswesen, 1972, Sep-28, Volume: 27, Issue:39

    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].
    Annales de biologie clinique, 1972, Volume: 30, Issue:6

    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].
    Monatsschrift fur Kinderheilkunde, 1971, Volume: 119, Issue:7

    Topics: Child, Preschool; Epilepsy, Tonic-Clonic; Humans; Metabolism, Inborn Errors; Pyridoxine; Tryptophan; Vitamin B 6 Deficiency

1971
[Pathogenesis of photodermatosis].
    Minerva medica, 1972, Apr-11, Volume: 63, Issue:27

    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.
    The Tohoku journal of experimental medicine, 1968, Volume: 94, Issue:1

    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.
    Biochimica et biophysica acta, 1969, Dec-23, Volume: 194, Issue:2

    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].
    Schweizerische medizinische Wochenschrift, 1970, Jul-04, Volume: 100, Issue:27

    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].
    Zeitschrift fur die gesamte innere Medizin und ihre Grenzgebiete, 1967, Mar-01, Volume: 22, Issue:5

    Topics: Hartnup Disease; Humans; Kynurenine; Metabolism, Inborn Errors; Tryptophan

1967
Vitamin B6 dependent xanthurenic aciduria (the second report).
    The Tohoku journal of experimental medicine, 1968, Volume: 95, Issue:2

    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].
    Annales de pediatrie, 1964, Mar-02, Volume: 11, Issue:3

    Topics: Humans; Indoles; Metabolism, Inborn Errors; Tryptophan

1964
[Biochemical and analytical bases of the exploration of phenylalanine metabolism].
    Annales de pediatrie, 1964, Mar-02, Volume: 11, Issue:3

    Topics: Humans; Intellectual Disability; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Tryptophan; Tyrosine

1964
["Borderline" forms of phenylketonuria].
    Annales de pediatrie, 1964, Mar-02, Volume: 11, Issue:3

    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].
    Deutsche Zeitschrift fur Verdauungs- und Stoffwechselkrankheiten, 1965, Volume: 25, Issue:4

    Topics: Asthma; Eczema; Humans; Kynurenic Acid; Leg Ulcer; Metabolism, Inborn Errors; Pyridoxine; Tryptophan; Urticaria; Xanthurenates

1965