tryptophan and Amino Acid Metabolism Disorders, Inborn

tryptophan has been researched along with Amino Acid Metabolism Disorders, Inborn in 86 studies

Research

Studies (86)

Timeframe	Studies, this research(%)	All Research%
pre-1990	62 (72.09)	18.7374
1990's	12 (13.95)	18.2507
2000's	7 (8.14)	29.6817
2010's	3 (3.49)	24.3611
2020's	2 (2.33)	2.80

Authors

Authors	Studies
Akasaka, Y; Ichioka, H; Ikegaya, H; Kondo, H; Kondou, H	1
Bernstein, L; Coughlin, CR; Drumm, M; Rohr, F; Yannicelli, S	1
Fukuwatari, T; Ohno, T; Sano, M; Shibata, K	1
Andrade, VS; de Andrade, RB; de Castro, FL; Garcia, C; Gemelli, T; Nunes, ML; Oliveira, L; Rojas, DB; Wannmacher, CM	1
Ashmore, C; Chakrapani, A; Daly, A; Gokmen-Ozel, H; Hendriksz, C; MacDonald, A; Preece, MA; Vijay, S	1
CSALAY, L; HORVATH, G; SOS, J	1
ASCHKENASY, A; NATAF, B	1
ARAKAWA, T; ITO, H; TADA, K; WADA, Y	1
BARNESS, LA; BESSELMAN, D; MELLMAN, WJ; TEDESCO, TA	1
CLODI, PH; DEUTSCH, E; NIEBAUER, G	1
DELAEY, P; HOOFT, C; SNOECK, J; TIMMERMANS, J	2
FOIS, A; LECCHINI, L	2
CLAMP, JR; KOMROWER, GM; WESTALL, RG; WILSON, V	1
ANDERSON, JA; DOEDEN, D; DRUMMOND, KN; GOOD, RA; MICHAEL, AF	1
DRUMMOND, KN; GOOD, RA; MICHAEL, AF; ULSTROM, RA	1
BICKEL, H	1
Cornelio, AR; de Souza Wyse, AT; Dutra-Filho, CS; Rodrigues, V; Wajner, M; Wannmacher, CM	1
Cornelio, A; Dutra-Filho, CS; Feksa, LR; Wajner, M; Wannmacher, CM; Wyse, AT	1
de Souza Wyse, AT; Dutra-Filho, CS; Feksa, LR; Latini, A; Rech, VC; Wajner, M; Wannmacher, CM	1
Cheng, KC; Connor, JR; Goodman, SI; Housman, C; Jacobs, RE; LaNoue, K; Lazovic, J; O'Callaghan, JP; Simpson, I; Woontner, M; Zinnanti, WJ	1
Amaral, MF; Dutra-Filho, CS; Feksa, LR; Feksa, PB; Koch, GD; Latini, A; Leipnitz, G; Rech, VC; Wajner, M; Wannmacher, CM	1
Komrower, GM; Westall, R	1
Benevenga, NJ; Steele, RD	1
Beemer, FA; Duran, M; Janssen, B; Wadman, SK; Wendel, U	1
Fenton, DA; Toseland, PA; Wilkinson, JD	1
Martin, JR; Mellor, CS; Snedden, W	2
Fraser, FC; Martin, JR; Mellor, CS	1
Inoue, F; Kinugasa, A; Matsuo, S; Sawada, T; Takeuchi, Y; Yoshioka, H	1
Endo, F; Hoshide, R; Ishikawa, K; Kato, I; Kiwaki, K; Koike, E; Komaki, S; Matsuura, T; Oyanagi, K; Suzuki, Y	1
Rohr, F; Warman, ML; Yannicelli, S	1
Cotton, RG; Dianzani, I; Howells, DW; Ponzone, A; Saleeba, JA; Smooker, PM	1
Dalton, RN; Howard, RS; Olpin, SE; Prevett, MC	1
Emons, D; Haverkamp, F; Kreft, B; Woelfle, J	1
Iguchi, T; Imai, J; Kawai, M; Murayama, K; Sakai, Y; Shimizu, H; Sumi, T; Yamaguchi, S; Yoshida, I	1
Takita, H	1
Krákorová, I; Makovicková, H; Marklová, E	1
Prats Viñas, J	1
Pratt, OE	1
Kamyshev, NG; Ponomarenko, VV; Smirnova, GP	1
Grimm, U; Knapp, A; Reddemann, H; Schlenzka, K; Schmitz, KW; Schmitz, W; Schulz, M; Smetan, M	1
Korzon, M; Korzon, T	1
Brandt, NJ; Christensen, E; Gregersen, N; Grøn, IH; Rasmussen, K	1
Kyllerman, M; Steen, G	1
Tada, K	1
Reddi, OS; Reddy, KR; Reddy, MV	1
Bhatti, A; Sur, AM	1
Barashnev, IuI; Grimm, U; Kazantseva, LZ; Knapp, A; Vel'tishchev, IuE	1
Batshaw, M; Brusilow, S; Kulovich, S; Nyhan, W; Spector, E; Thoene, J; Walser, M	1
Brandt, NJ; Brandt, S; Christensen, E; Gregersen, N; Gron, I; Rasmussen, K	1
Breslich, DJ; Goodman, SI; Moe, PG; Norenberg, MD; Shikes, RH	1
Gates, SC; Higgins, JV; Wilson, CM; Wilson, RW	1
Grimm, U; Knapp, A; Machill, G; Reddemann, H; Schlenzka, K; Schmitz, KW; Schmitz, W; Schulz, M; Smetan, M	1
Inoue, F; Kinugasa, A; Kodo, N; Matsuo, S; Sawada, T; Takeuchi, Y; Yamanaka, H; Yoshioka, H	1
Chen, Y; Wu, L; Xiong, Q	1
Kakinuma, H; Sato, H; Tsuchiya, M; Yokoyama, Y	1
Batshaw, ML; Coyle, JT; Hyman, SL; Jankel, W; Parke, JC; Porter, C; Thomas, GH	1
Colombo, JP	1
Berbis, P; Garnier, JP; Jouve, I; Privat, Y	1
Bender, DA; McCreanor, GM; Salih, MA	1
Francois, J	1
Chiancone, FM; Mainardi, L; Tenconi, LT	1
Brissaud, HE	1
Binazzi, M; Calandra, P	1
Kruglov, BV; Lebedev, VP; Levitina, NO; Tabolin, VA	1
Boisse, J; Moatti, N	1
Tabolin, VA	1
Hategan, D; Luca, N; Voiculescu, V	1
Nair, KR; Virmani, V	1
Price, JM	1
Menne, F	1
Buist, NR; Ferry, PC; Ramberg, DA; Strandholm, JJ	1
Kahn, LI	1
Carpenter, DG; Carter, CH	1
Knapp, A	1
Arakawa, T; Nakagawa, H; Tada, K; Yokoyama, Y; Yoshida, T	1
Heilmann, HH; Knapp, A; Wolfram, G	1
Gusev, EI	1
Orsini, A; Perrimond, H; Pierron, H; Vovan, L	1
Scriver, CR; Whelan, DT	1
Jérôme, H	1
Tada, K; Yokoyama, Y	1
Gershon, ES; Shader, RI	1

Reviews

13 review(s) available for tryptophan and Amino Acid Metabolism Disorders, Inborn

Article	Year
Adverse effects of excessive consumption of amino acids. Annual review of nutrition, 1984, Volume: 4 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Brain; Cattle; Diet; Disease Models, Animal; Ethionine; Fenclonine; Glycine; Growth Disorders; Histidine; Humans; Methionine; Nerve Tissue Proteins; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Pneumonia, Atypical Interstitial, of Cattle; Serine; Stereoisomerism; Sulfhydryl Compounds; Tissue Distribution; Tryptophan; Tyrosine; Vitamin A	1984
Nutrition support for glutaric acidemia type I. Journal of the American Dietetic Association, 1994, Volume: 94, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Child; Child, Preschool; Dietary Proteins; Female; Food, Formulated; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant; Infant, Newborn; Lysine; Male; Mitochondria; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Riboflavin; Tryptophan	1994
[Blue diaper syndrome]. Ryoikibetsu shokogun shirizu, 1998, Issue:19 Pt 2 Topics: Amino Acid Metabolism, Inborn Errors; Biomarkers; Diagnosis, Differential; Humans; Indigo Carmine; Indoles; Infant; Infant, Newborn; Prognosis; Syndrome; Tryptophan	1998
The transport of metabolizable substances into the living brain. Advances in experimental medicine and biology, 1976, Volume: 69 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Biological Transport, Active; Blood Glucose; Blood-Brain Barrier; Brain; Glucose; Haplorhini; Humans; Hyperglycemia; Insulin; Ketone Bodies; Lactates; Neurotransmitter Agents; Papio; Phenylalanine; Pyruvates; Rats; Renal Aminoacidurias; Thyroid Hormones; Tryptophan	1976
[Clinical importance of tryptophan metabolism disorders]. Polski tygodnik lekarski (Warsaw, Poland : 1960), 1978, May-08, Volume: 33, Issue:19 Topics: Amino Acid Metabolism, Inborn Errors; Hartnup Disease; Humans; Neoplasms; Pyridoxine; Tryptophan; Tryptophan Oxygenase; Vitamin B 6 Deficiency; Xanthurenates	1978
Urea cycle disorders, hyperammonemia and neurotransmitter changes. Enzyme, 1987, Volume: 38, Issue:1-4 Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Animals; Brain Chemistry; Rats; Serotonin; Tryptophan	1987
[Disorders of tryptophan metabolism in dermatology]. Annales de dermatologie et de venereologie, 1987, Volume: 114, Issue:12 Topics: Amino Acid Metabolism, Inborn Errors; Humans; Skin Diseases; Tryptophan	1987
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
[Chief clinical syndromes in children with tryptophan metabolism disorders (literature survey)]. Voprosy okhrany materinstva i detstva, 1972, Volume: 17, Issue:6 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Carboxy-Lyases; Child; Child, Preschool; Diabetes Mellitus; Glutamates; Hartnup Disease; Humans; Hydrolases; Intestinal Absorption; Intestinal Mucosa; Kidney; Kynurenine; Liver; Metabolic Diseases; Neurologic Manifestations; Nicotinic Acids; ortho-Aminobenzoates; Pyridoxal; Pyridoxine; Skin Manifestations; Tryptophan; Vitamin B 6 Deficiency; Xanthurenates	1972
[Amino acid transfer systems and their importance in pathology. II. Specific abnormalities in renal and intestinal amino acid transfer]. Annales de biologie clinique, 1973, Volume: 31, Issue:4 Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Cystine; Female; Glycine; Hartnup Disease; Humans; Infant; Lysine; Malabsorption Syndromes; Male; Methionine; Renal Tubular Transport, Inborn Errors; Tryptophan	1973
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
Factors which alter the metabolism of tryptophan. Medical journal of Osaka University, 1968, Volume: 19, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Animals; Contraceptives, Oral; Female; Humans; Kynurenine; Nicotinic Acids; Tryptophan; Vitamin B 6 Deficiency; Xanthurenates	1968
[Feeble mindedness caused by genetic disorders of amino acid metabolism]. Hippokrates, 1968, May-31, Volume: 39, Issue:10 Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Citrulline; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Hydroxyproline; Intellectual Disability; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Proline; Sarcosine; Succinates; Transferases; Tryptophan; Valine	1968

Other Studies

73 other study(ies) available for tryptophan and Amino Acid Metabolism Disorders, Inborn

Article	Year
Sudden death of a 2-year-old child due to alpha-ketoadipic aciduria. Forensic science, medicine, and pathology, 2022, Volume: 18, Issue:4 Topics: Adipates; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Death, Sudden; Humans; Lysine; Male; Tryptophan	2022
Inconsistencies in the Nutrition Management of Glutaric Aciduria Type 1: An International Survey. Nutrients, 2020, Oct-16, Volume: 12, Issue:10 Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Child; Child Nutritional Physiological Phenomena; Child, Preschool; Diet Therapy; Dietary Proteins; Female; Glutaryl-CoA Dehydrogenase; Humans; Infant; Infant Nutritional Physiological Phenomena; Infant, Newborn; Lysine; Male; Practice Guidelines as Topic; Recommended Dietary Allowances; Surveys and Questionnaires; Tryptophan	2020
The urinary ratio of 3-hydroxykynurenine/3-hydroxyanthranilic acid is an index to predicting the adverse effects of D-tryptophan in rats. Journal of nutritional science and vitaminology, 2014, Volume: 60, Issue:4 Topics: 3-Hydroxyanthranilic Acid; Amino Acid Metabolism, Inborn Errors; Animals; Diet; Hydrolases; Kynurenine; Male; Rats, Wistar; Tryptophan; Weight Gain	2014
Creatine and pyruvate prevent behavioral and oxidative stress alterations caused by hypertryptophanemia in rats. Molecular and cellular biochemistry, 2012, Volume: 362, Issue:1-2 Topics: Amino Acid Metabolism, Inborn Errors; Animals; Behavior, Animal; Creatine; Male; Oxidative Stress; Pyruvic Acid; Rats; Rats, Wistar; Tryptophan	2012
Dietary practices in glutaric aciduria type 1 over 16 years. Journal of human nutrition and dietetics : the official journal of the British Dietetic Association, 2012, Volume: 25, Issue:6 Topics: Adolescent; Adult; Age Factors; Amino Acid Metabolism, Inborn Errors; Biomarkers; Brain Diseases; Brain Diseases, Metabolic; Carnitine; Child; Child, Preschool; Diet, Protein-Restricted; Dietary Proteins; Dietetics; Disabled Persons; Early Diagnosis; Enteral Nutrition; Female; Glucose; Glutaryl-CoA Dehydrogenase; Humans; Lysine; Male; Practice Patterns, Physicians'; Severity of Illness Index; Tryptophan; United Kingdom; Young Adult	2012
[Mechanism of histamine resistance due to amino acid deficiency]. Kiserletes orvostudomany, 1954, Volume: 6, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Biochemical Phenomena; Histamine; Histamine Agents; Methionine; Tryptophan	1954
[Effects exercised on the rat by the exclusive deprivation of sulfurated amino acids, of lysine or of tryptophan on the power to concentrate iodides by the thyroid in the absence of any dietary iodine]. Comptes rendus des seances de la Societe de biologie et de ses filiales, 1961, Volume: 155 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Antifibrinolytic Agents; Iodides; Iodine; Lysine; Rats; Thyroid Gland; Tryptophan; Viscera	1961
CONGENITAL TRYPTOPHANURIA WITH DWARFISM ("H" DISEASE-LIKE CLINICAL FEATURES WITHOUT INDICANURIA AND GENERALIZED AMINOACIDURIA):--A PROBABLY NEW INBORN ERROR OF TRYPTOPHAN METABOLISM. The Tohoku journal of experimental medicine, 1963, Jul-25, Volume: 80 Topics: Amino Acid Metabolism, Inborn Errors; Ataxia; Dwarfism; Genetics, Medical; Humans; Intellectual Disability; Metabolic Diseases; Tryptophan; Urine	1963
INDOLYLACROYL GLYCINE EXCRETION IN A FAMILY WITH MENTAL RETARDATION. Clinica chimica acta; international journal of clinical chemistry, 1963, Volume: 8 Topics: Amino Acid Metabolism, Inborn Errors; Body Fluids; Child; Glycine; Humans; Hydrogen-Ion Concentration; Indoles; Intellectual Disability; Kidney; Neomycin; Pharmacology; Proteins; Renal Aminoacidurias; Tryptophan; Urine	1963
[A CLINICAL PICTURE WITH POIKILODERMA-LIKE SKIN CHANGES, AMINOACIDURIA AND INDOLACETURIA. CONTRIBUTION TO DATA ON HARTNUP SYNDROME]. Archiv fur klinische und experimentelle Dermatologie, 1964, Jan-15, Volume: 218 Topics: Amino Acid Metabolism, Inborn Errors; Chromatography; Dermatology; Humans; Indoles; Infant; Metabolic Diseases; Renal Aminoacidurias; Tryptophan; Urine	1964
BIOCHEMICAL ASPECTS OF THE HARTNUP DISEASE. I. RESULTS OF INTRAVENOUS AND ORAL TRYPTOPHAN LOADING TESTS IN A CASE OF HARTNUP DISEASE. Annales paediatrici. International review of pediatrics, 1964, Volume: 202 Topics: Amino Acid Metabolism, Inborn Errors; Biomedical Research; Friedreich Ataxia; Genetics, Medical; Hartnup Disease; Humans; Indican; Indoles; Infant; Intestines; Metabolic Diseases; Neomycin; Niacin; Niacinamide; Nicotinic Acids; Nystatin; Pellagra; Renal Aminoacidurias; Tryptophan; Urine	1964
[URINARY ELIMINATION OF THE METABOLITES OF TRYPTOPHAN IN NEUROLOGICAL DISEASES IN CHILDREN. 1. RESULTS IN HYPSARRHYTHMIA, EPILEPSY AND MENTAL RETARDATION WITHOUT CONVULSIONS]. Rivista di clinica pediatrica, 1963, Volume: 72 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Child; Chromatography; Epilepsy; Humans; Infant; Infant, Newborn; Intellectual Disability; Metabolism; Renal Aminoacidurias; Seizures; Spasms, Infantile; Tryptophan; Urine; Xanthurenates	1963
BIOCHEMICAL ASPECTS OF THE HARTNUP DISEASE. III. GENERAL DISCUSSION AND CONCLUSIONS. Annales paediatrici. International review of pediatrics, 1964, Volume: 202 Topics: Amino Acid Metabolism, Inborn Errors; Child; Drug Therapy; Feces; Hartnup Disease; Humans; Indican; Indoles; Metabolic Diseases; Niacin; Niacinamide; Nicotinic Acids; Pellagra; Renal Aminoacidurias; Tryptophan; Urine	1964
HYDROXYKYNURENINURIA: A CASE OF ABNORMAL TRYPTOPHAN METABOLISM PROBABLY DUE TO A DEFICIENCY OF KYNURENINASE. Archives of disease in childhood, 1964, Volume: 39 Topics: Amino Acid Metabolism, Inborn Errors; Child; Chromatography; Electrophoresis; Humans; Hydrolases; Kynurenic Acid; Kynurenine; Metabolic Diseases; Niacin; ortho-Aminobenzoates; Proteins; Pyridoxine; Spectrophotometry; Tryptophan; Urine; Xanthurenates	1964
ACUTE CEREBELLAR ATAXIA ASSOCIATED WITH SOME FEATURES OF THE HARTNUP SYNDROME. PRESENTATION OF A CASE. Helvetica paediatrica acta, 1964, Volume: 19 Topics: Amino Acid Metabolism, Inborn Errors; Cerebellar Ataxia; Child; Chromatography; Drug Therapy; Electroencephalography; Friedreich Ataxia; Hartnup Disease; Humans; Indoles; Italy; Neomycin; Niacin; Nicotinic Acids; Nystagmus, Pathologic; Renal Aminoacidurias; Tryptophan; Urine	1964
TRYPTOPHAN METABOLISM IN MAN. The Journal of clinical investigation, 1964, Volume: 43 Topics: Amino Acid Metabolism, Inborn Errors; Calcium; Child; Glucuronates; Humans; Indican; Indoleacetic Acids; Intestinal Absorption; Kynurenine; Male; Metabolism; ortho-Aminobenzoates; p-Aminohippuric Acid; Pyridines; Tryptophan; Urine; Xanthurenates	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
[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
Tryptophan reduces creatine kinase activity in the brain cortex of rats. International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience, 2004, Volume: 22, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases, Metabolic, Inborn; Cerebral Cortex; Creatine Kinase; Disease Models, Animal; Down-Regulation; Energy Metabolism; Glutathione; Oxidative Stress; Rats; Rats, Wistar; Tryptophan	2004
The effects of the interactions between amino acids on pyruvate kinase activity from the brain cortex of young rats. International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience, 2005, Volume: 23, Issue:6 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Binding Sites; Brain Diseases, Metabolic, Inborn; Cerebral Cortex; Cystine; Energy Metabolism; Feedback, Physiological; Nerve Degeneration; Phenylalanine; Pyruvate Kinase; Rats; Rats, Wistar; Serine; Tryptophan	2005
Promotion of oxidative stress by L-tryptophan in cerebral cortex of rats. Neurochemistry international, 2006, Volume: 49, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Animals; Antioxidants; Catalase; Cerebral Cortex; Disease Models, Animal; Down-Regulation; Enzyme Inhibitors; Free Radicals; Glutathione; Lipid Peroxidation; Luminescence; Male; Nerve Degeneration; NG-Nitroarginine Methyl Ester; Nitric Oxide Synthase Type I; Oxidative Stress; Rats; Rats, Wistar; Superoxide Dismutase; Thiobarbituric Acid Reactive Substances; Tryptophan	2006
Mechanism of age-dependent susceptibility and novel treatment strategy in glutaric acidemia type I. The Journal of clinical investigation, 2007, Volume: 117, Issue:11 Topics: Aging; Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases, Metabolic, Inborn; Child; Diet; Disease Models, Animal; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glucose; Glutamic Acid; Glutarates; Glutaryl-CoA Dehydrogenase; Homoarginine; Humans; Lysine; Mice; Mice, Knockout; Mitochondria; Neurons; Nuclear Magnetic Resonance, Biomolecular; Tryptophan	2007
Tryptophan administration induces oxidative stress in brain cortex of rats. Metabolic brain disease, 2008, Volume: 23, Issue:2 Topics: alpha-Tocopherol; Amino Acid Metabolism, Inborn Errors; Animals; Antioxidants; Brain Diseases, Metabolic; Catalase; Cell Death; Cerebral Cortex; Disease Models, Animal; Glutathione; Glutathione Peroxidase; Male; Nerve Degeneration; Neurons; Oxidative Stress; Rats; Rats, Wistar; Superoxide Dismutase; Superoxide Dismutase-1; Taurine; Thiobarbituric Acid Reactive Substances; Tryptophan	2008
Hydroxykynureninuria. American journal of diseases of children (1960), 1967, Volume: 113, Issue:1 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Female; Growth; Humans; Infant, Newborn; Intelligence Tests; Kynurenic Acid; Kynurenine; Kyphosis; Nicotinic Acids; Pyridoxine; Tryptophan; Xanthurenates	1967
A patient with alpha-ketoadipic and alpha-aminoadipic aciduria. Journal of inherited metabolic disease, 1984, Volume: 7, Issue:2 Topics: 2-Aminoadipic Acid; Adipates; Amino Acid Metabolism, Inborn Errors; Amino Acids, Dicarboxylic; Child; Dietary Proteins; Fibroblasts; Humans; Lysine; Male; Pipecolic Acids; Tryptophan	1984
Family exhibiting cerebellar-like ataxia, photosensitivity and shortness of stature - a new inborn error of tryptophan metabolism. Journal of the Royal Society of Medicine, 1983, Volume: 76, Issue:9 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Body Height; Cerebellar Ataxia; Child; Female; Humans; Male; Photosensitivity Disorders; Syndrome; Tryptophan	1983
Familial hypertryptophanemia, tryptophanuria and indoleketonuria. Clinica chimica acta; international journal of clinical chemistry, 1983, Jul-15, Volume: 131, Issue:3 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Chromatography, Gas; Chromatography, High Pressure Liquid; Female; Gas Chromatography-Mass Spectrometry; Humans; Indoles; Male; Tryptophan	1983
Hypertryptophanemia and indoleketonuria in two mentally subnormal siblings. The New England journal of medicine, 1982, Nov-25, Volume: 307, Issue:22 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Humans; Indoleacetic Acids; Indoles; Intellectual Disability; Tryptophan	1982
Familial hypertryptophanemia in two siblings. Clinical genetics, 1995, Volume: 47, Issue:4 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Female; Humans; Male; Pedigree; Psychological Tests; Tryptophan	1995
Efficacy of tryptophan for the treatment of nonketotic hyperglycinemia: a new therapeutic approach for modulating the N-methyl-D-aspartate receptor. Pediatrics, 1995, Volume: 95, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Electroencephalography; Female; Glycine; Humans; Tryptophan	1995
Four newly identified ornithine transcarbamylase (OTC) mutations (D126G, R129H, I172M and W332X) in Japanese male patients with early-onset OTC deficiency. Human mutation, 1994, Volume: 3, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Aspartic Acid; Base Sequence; DNA Mutational Analysis; DNA Primers; DNA, Single-Stranded; Glycine; Histidine; Humans; Infant; Infant, Newborn; Isoleucine; Male; Methionine; Molecular Epidemiology; Molecular Sequence Data; Nucleic Acid Conformation; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Tryptophan; X Chromosome	1994
Two new mutations in the dihydropteridine reductase gene in patients with tetrahydrobiopterin deficiency. Journal of medical genetics, 1993, Volume: 30, Issue:6 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acid Sequence; Aspartic Acid; Base Sequence; Biopterins; Conserved Sequence; Dihydropteridine Reductase; DNA Mutational Analysis; Glycine; Humans; Infant; Infant, Newborn; Male; Molecular Sequence Data; Nucleic Acid Heteroduplexes; Point Mutation; Tryptophan	1993
Glutaric aciduria type 1 in adulthood. Journal of neurology, neurosurgery, and psychiatry, 1996, Volume: 60, Issue:3 Topics: Amino Acid Metabolism, Inborn Errors; Dystonia; Female; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Lysine; Middle Aged; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Tryptophan	1996
Subdural hemorrhage as an initial sign of glutaric aciduria type 1: a diagnostic pitfall. Pediatric radiology, 1996, Volume: 26, Issue:11 Topics: Amino Acid Metabolism, Inborn Errors; Atrophy; Cisterna Magna; Developmental Disabilities; Diagnosis, Differential; Female; Frontal Lobe; Glutarates; Glutaryl-CoA Dehydrogenase; Hematoma, Subdural; Humans; Infant; Lysine; Magnetic Resonance Imaging; Movement Disorders; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Psychomotor Performance; Temporal Lobe; Tomography, X-Ray Computed; Tryptophan	1996
Determination of the 8-methyl ether of xanthurenic acid in human serum by high-performance liquid chromatography with fluorescence detection. Journal of chromatography. B, Biomedical applications, 1996, Apr-26, Volume: 679, Issue:1-2 Topics: Amino Acid Metabolism, Inborn Errors; Chromatography, High Pressure Liquid; Ethers; Humans; Kynurenine; Sensitivity and Specificity; Silicon Dioxide; Spectrometry, Fluorescence; Tryptophan; Xanthurenates	1996
Screening for defects in tryptophan metabolism. Journal of chromatography. A, 2000, Feb-18, Volume: 870, Issue:1-2 Topics: Amino Acid Metabolism, Inborn Errors; Chromatography, High Pressure Liquid; Chromatography, Thin Layer; Humans; Sensitivity and Specificity; Spectrophotometry, Ultraviolet; Tryptophan	2000
[Glutaric aciduria type I: an organic acidemia without acidosis with severe movement disorders]. Neurologia (Barcelona, Spain), 2001, Volume: 16, Issue:8 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Carnitine; Child, Preschool; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant; Lysine; Movement Disorders; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Phenotype; Tryptophan	2001
[Motor activity of tryptophan--xanthommatin metabolic pathway mutants in Drosophila melanogaster]. Doklady Akademii nauk SSSR, 1979, Volume: 246, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Animals; Disease Models, Animal; Drosophila melanogaster; Kynurenine; Metamorphosis, Biological; Motor Activity; Mutation; Tryptophan	1979
[Tryptophan metabolism and oligophrenia (author's transl)]. Fortschritte der Neurologie, Psychiatrie, und ihrer Grenzgebiete, 1978, Volume: 46, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Down Syndrome; Epilepsy; Hartnup Disease; Humans; Intellectual Disability; Kynurenine; Pyridoxine; Tryptophan; Xanthurenates	1978
Treatment of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria). Experience with diet, riboflavin, and GABA analogue. The Journal of pediatrics, 1979, Volume: 94, Issue:4 Topics: 2-Aminoadipic Acid; Amino Acid Metabolism, Inborn Errors; Aminobutyrates; Baclofen; Child; Diet Therapy; Dietary Proteins; Female; Glutarates; Humans; Lysine; Male; Oxidoreductases; Riboflavin; Tryptophan	1979
Intermittently progressive dyskinetic syndrome in glutaric aciduria. Neuropadiatrie, 1977, Volume: 8, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Animals; Child; Child, Preschool; Female; Glutarates; Humans; Infant; Infant, Newborn; Language Disorders; Lysine; Movement Disorders; Rabbits; Tryptophan	1977
[Blue diaper syndrome]. Nihon rinsho. Japanese journal of clinical medicine, 1977,Spring, Volume: 35 Suppl 1 Topics: Amino Acid Metabolism, Inborn Errors; Humans; Indican; Infant; Infant, Newborn; Tryptophan	1977
Familial hydroxykynureninuria. Human heredity, 1978, Volume: 28, Issue:3 Topics: Amino Acid Metabolism, Inborn Errors; Child; Consanguinity; Female; Gingival Diseases; Humans; Intellectual Disability; Kynurenine; Male; Pedigree; Stomatitis; Syndrome; Tryptophan; Xanthurenates	1978
Indian childhood cirrhosis: an inherited disorder of tryptophan metabolism? British medical journal, 1978, Aug-19, Volume: 2, Issue:6136 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Child; Ethnicity; Humans; India; Liver Cirrhosis; Tryptophan	1978
[Role of tryptophan metabolism disorders in the etiology of mental retardation in children]. Voprosy okhrany materinstva i detstva, 1978, Volume: 23, Issue:10 Topics: Adolescent; Adult; Aged; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Female; Humans; Intellectual Disability; Male; Middle Aged; Pedigree; Tryptophan	1978
Neonatal citrllinemia: treatment with keto-analogues of essential amino acids. The Journal of pediatrics, 1977, Volume: 90, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Essential; Arginine; Argininosuccinate Synthase; Citrulline; Fibroblasts; Histidine; Humans; Infant; Infant, Newborn; Isoleucine; Leucine; Lysine; Male; Methionine; Phenylalanine; Threonine; Tryptophan; Valine	1977
Glutaric aciduria: clinical and laboratory findings in two brothers. The Journal of pediatrics, 1977, Volume: 90, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Cerebral Palsy; Child; Child, Preschool; Coenzyme A; Consanguinity; Glutarates; Humans; Hydroxylysine; Infant; Infant, Newborn; Lysine; Male; Oxidoreductases; Tryptophan	1977
Glutaric aciduria: biochemical and morphologic considerations. The Journal of pediatrics, 1977, Volume: 90, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Autopsy; Brain; Brain Chemistry; Child; Glutarates; Humans; Hydroxylysine; Infant; Kidney; Liver; Lysine; Male; Mitochondria, Liver; Myocardium; Oxidoreductases; Tryptophan	1977
Alpha-ketoadipic aciduria: a description of a new metabolic error in lysine-tryptophan degradation. Pediatric research, 1975, Volume: 9, Issue:6 Topics: Adipates; Adolescent; Amino Acid Metabolism, Inborn Errors; Humans; Intellectual Disability; Keto Acids; Lysine; Male; Tryptophan	1975
[Determination of kynureninase activity in oligophrenic children with hereditary taint, before and after vitamin B6 treatment]. Acta biologica et medica Germanica, 1975, Volume: 34?710 Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child; Humans; Hydrolases; Intellectual Disability; Kynurenine; Pyridoxine; Tryptophan	1975
Tryptophan therapy for non-ketotic hyperglycinaemia. Journal of inherited metabolic disease, 1992, Volume: 15, Issue:3 Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Female; Glycine; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Tryptophan	1992
The ocular abnormalities of blue diaper syndrome. Metabolic, pediatric, and systemic ophthalmology (New York, N.Y. : 1985), 1991, Volume: 14, Issue:3-4 Topics: Amino Acid Metabolism, Inborn Errors; Calcinosis; Child; Eye Abnormalities; Humans; Hypercalcemia; Kidney Diseases; Male; Pedigree; Syndrome; Tryptophan; Visual Acuity	1991
Simultaneous determination of urinary creatinine and aromatic amino acids by cation-exchange chromatography with ultraviolet detection. Journal of chromatography, 1991, May-03, Volume: 566, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Cations; Chromatography, High Pressure Liquid; Chromatography, Ion Exchange; Creatinine; Humans; Infant, Newborn; Phenylalanine; Phenylketonurias; Tryptophan; Tyrosine	1991
Anorexia and altered serotonin metabolism in a patient with argininosuccinic aciduria. The Journal of pediatrics, 1986, Volume: 108, Issue:5 Pt 1 Topics: Amino Acid Metabolism, Inborn Errors; Anorexia; Arginine; Argininosuccinic Acid; Child; Dietary Proteins; Feeding and Eating Disorders; Feeding Behavior; Female; Humans; Hydroxyindoleacetic Acid; Serotonin; Sleep, REM; Tryptophan	1986
Lethal familial pellagra-like skin lesion associated with neurologic and developmental impairment and the development of cataracts. Pediatrics, 1985, Volume: 76, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Cataract; Cerebellar Ataxia; Child, Preschool; Consanguinity; Diagnosis, Differential; Female; Humans; Infant; Intellectual Disability; Male; Pedigree; Pellagra; Skin; Syndrome; Tryptophan	1985
[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
[Dietetics of amino acid metabolism disorders]. La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris, 1971, Feb-08, Volume: 47, Issue:7 Topics: Amino Acid Metabolism, Inborn Errors; Diet Therapy; Glycine; Histidine; Homocystinuria; Humans; Isoleucine; Leucine; Phenylketonurias; Tryptophan; Tyrosine; Valine	1971
Tryptophan metabolsim and serum fatty acids in acrodermatitis enteropathica. Archiv fur dermatologische Forschung, 1974, Jun-11, Volume: 249, Issue:4 Topics: Acrodermatitis; Adolescent; Amino Acid Metabolism, Inborn Errors; Aminohippuric Acids; Arachidonic Acids; Child; Child, Preschool; Fatty Acids; Female; Humans; Indoles; Kynurenic Acid; Kynurenine; Linoleic Acids; Malabsorption Syndromes; Male; ortho-Aminobenzoates; Paronychia; Pyridoxine; Quinolines; Tryptophan; Xanthurenates	1974
[Metabolic disorders, their early diagnosis and therapy in newborn infants]. Vestnik Akademii meditsinskikh nauk SSSR, 1973, Volume: 28, Issue:6 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
Biochemical research in two cases of endogenous pellagra. European neurology, 1973, Volume: 10, Issue:4 Topics: Adult; Alanine Transaminase; Amino Acid Metabolism, Inborn Errors; Amino Acids; Aspartate Aminotransferases; Blood Proteins; Humans; Hydroxyindoleacetic Acid; Indican; Male; Middle Aged; Pellagra; Serotonin; Tryptophan	1973
Newer trends in the genetic and biochemical studies in the etiopathogenesis of aminoacidopathies. Neurology India, 1973, Volume: 21, Issue:3 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Base Sequence; Coenzymes; DNA; Enzymes; Genes, Regulator; Humans; Infant; Leucine; Mutation; Pyridoxine; Syndrome; Tryptophan; Vitamin B 12	1973
Copper poppers: a benign cause of blue diapers. Archives of disease in childhood, 1971, Volume: 46, Issue:250 Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Clothing; Color; Copper; Female; Humans; Infant; Malabsorption Syndromes; Tryptophan	1971
From the Clinical Conference St. Louis Children's Hospital. Phenylketonuria. Diagnostic and therapeutic dilemma. Clinical pediatrics, 1970, Volume: 9, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Diet Therapy; Female; Humans; Infant; Intellectual Disability; Phenylalanine; Phenylketonurias; Transaminases; Tryptophan; Tyrosine	1970
Inborn errors of metabolism associated with unusual odors. The Journal of the Florida Medical Association, 1970, Volume: 57, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Fatty Acids; Female; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Malabsorption Syndromes; Maple Syrup Urine Disease; Methionine; Odorants; Phenylalanine; Tryptophan; Valerates	1970
[Skin manifestations in genetic disturbances of the amino acid metabolism]. Dermatologische Monatschrift, 1970, Volume: 156, Issue:5 Topics: Albinism; Amino Acid Metabolism, Inborn Errors; Humans; Melanins; Pigmentation Disorders; Skin Manifestations; Tryptophan	1970
Vitamin B6 dependent xanthurenic aciduria. The Tohoku journal of experimental medicine, 1967, Volume: 93, Issue:2 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Aspartate Aminotransferases; Autoanalysis; Child; Child, Preschool; Chromatography, Thin Layer; Electroencephalography; Female; Humans; Hydrolases; Intellectual Disability; Kynurenic Acid; Liver; Male; Pedigree; Pyridoxal Phosphate; Pyridoxine; Tryptophan; Xanthurenates	1967
[On the pathology of tryptophan metabolism, with a report of another family with a deficiency simulating vitamin B6 deficiency]. Das Deutsche Gesundheitswesen, 1967, Dec-28, Volume: 22, Issue:52 Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child; Diagnosis, Differential; Female; Humans; Male; Tryptophan; Vitamin B 6 Deficiency	1967
[Hyperaminoaciduria in children suffering from progressive muscular dystrophy]. Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952), 1967, Volume: 67, Issue:7 Topics: Adolescent; Alanine; Amino Acid Metabolism, Inborn Errors; Arginine; Aspartic Acid; Child; Child, Preschool; Creatine; Creatinine; Female; Glutamates; Histidine; Humans; Leucine; Lysine; Male; Methionine; Muscular Dystrophies; Nitrogen; Phenylalanine; Serine; Threonine; Tryptophan; Tyrosine; Valine	1967
[Study of amino-aciduria and amino-acidemia in children by chromato-ionophoresis]. Marseille medical, 1967, Volume: 104, Issue:10 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Chromatography; Electrophoresis; Histidine; Humans; Phenylalanine; Tryptophan	1967
Cystathioninuria and renal iminoglycinuria in a pedigree. The New England journal of medicine, 1968, Apr-25, Volume: 278, Issue:17 Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child; Chromatography, Ion Exchange; Chromatography, Paper; Counseling; Female; Glycine; Heterozygote; Humans; Hydroxyproline; Infant; Infant, Newborn; Jaundice; Jews; Male; Metabolic Clearance Rate; Methionine; Middle Aged; Pedigree; Phenotype; Proline; Pyridoxine; Renal Aminoacidurias; Tryptophan	1968
[Abnormalities of the tryptophan metabolism in trisomy 21]. L'union medicale du Canada, 1968, Volume: 97, Issue:7 Topics: Amino Acid Metabolism, Inborn Errors; Humans; Trisomy; Tryptophan	1968
[B6-dependent xanthurenic aciduria]. Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme, 1968, Volume: 13, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Female; Humans; Liver; Male; Pyridoxine; Tryptophan; Xanthurenates	1968
Screening for aminoacidurias in psychiatric inpatients. Archives of general psychiatry, 1969, Volume: 21, Issue:1 Topics: Affective Symptoms; Amino Acid Metabolism, Inborn Errors; Brain Damage, Chronic; Depression; Drug Synergism; Hartnup Disease; Homocystinuria; Hospitals, Psychiatric; Humans; Intellectual Disability; Mass Screening; Massachusetts; Mental Disorders; Methionine; Monoamine Oxidase Inhibitors; Neurotic Disorders; Personality Disorders; Phenylketonurias; Schizophrenia; Substance-Related Disorders; Tryptophan	1969