tryptophan and Inborn Errors of Metabolism

tryptophan has been researched along with Inborn Errors of Metabolism 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 Inborn Errors of Metabolism

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 Inborn Errors of Metabolism

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