tryptophan and Amino Acid Transport Disorder, Neutral

tryptophan has been researched along with Amino Acid Transport Disorder, Neutral in 64 studies

Research

Studies (64)

Timeframe	Studies, this research(%)	All Research%
pre-1990	56 (87.50)	18.7374
1990's	5 (7.81)	18.2507
2000's	3 (4.69)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
CRAWFORD, MA; GIRAO, CB; LOUGHRIDGE, LW; MILNE, MD	1
HALVORSEN, K; HALVORSEN, S	1
ASATOOR, AM; CRASKE, J; LONDON, DR; MILNE, MD	1
REDDY, V; SRIKANTIA, SG; VENKATACHALAM, PS	1
DEMEULEMEESTER, F	1
HJELT, L; LAHIKAINEN, T; OHMAN, S; VISAKORPI, JK	1
DELAEY, P; HOOFT, C; SNOECK, J; TIMMERMANS, J	3
FOIS, A; LECCHINI, L	1
KIMMIG, J	1
HERSOV, LA; RODNIGHT, R	1
Milovanović, DD	1
Ohura, T	1
Jones, PM; Lambert, AM; Pillai, PM; Wong, PW	1
Bender, DA	1
Bielenberg, J	1
Takita, H	1
Dakeishi, M; Inoue, K; Koizumi, A; Manabe, M; Nozaki , J; Ohura, T; Wada, Y	1
Caspary, WF	1
Grimm, U; Knapp, A; Reddemann, H; Schlenzka, K; Schmitz, KW; Schmitz, W; Schulz, M; Smetan, M	1
Korzon, M; Korzon, T	1
Dickerson, JW; Wiryanti, J	1
Clifton, JA	1
Baru, IM; Shul'ga, IuD	1
Alpers, DH; Armbrustmacher, V; Feigin, RD; Prensky, AL; Tahmoush, AJ	1
Darby, WJ; McNutt, KW; Todhunter, EN	1
Aubry, P; Hernandorena, X; Le Bras, R; Thomas, J; Zimmer, C	1
Brune, GG; Pflughaupt, KW	1
Bachmann, C; Endres, W; Hadorn, HB; Herschkowitz, N; Ibel, H; Plöchl, E; Roscher, A; Schmidtke, K	1
Milovanović, DD; Milovanović, L; Radulović, D; Stanković, B	1
Butler, IJ; Jonas, AJ	1
Furuya, T; Orihara, T; Tochikubo, K; Tsuchiya, K	1
Baudin, B; Bodin, F; Coudray-Lucas, C; Giboudeau, J; Nguyen Dinh, F; Valla, D	1
Arakawa, T; Morikawa, T; Tada, K	1
Kitabatake, M; Nakao, T; Oyanagi, K; Takagi, M	1
Attal, C; Boisse, J; Charpentier, C; Lévy, H; Mozziconacci, P	1
Jepson, JB	1
Milne, MD	2
Asatoor, AM; Navab, F	1
Brune, GG; Brune, RM; Wiskemann, A	1
Kniazev, IuA; Vakhrusheva, LL	1
Mandell, AJ; Spooner, CE	1
Kruglov, BV; Lebedev, VP; Levitina, NO; Tabolin, VA	1
Boisse, J; Moatti, N	1
Antener, I; Bartelheimer, HK; Grüttner, R; Rybak, C	1
Alpers, DH; Thier, SO	1
Menne, F	1
Groth, U; Rosenberg, LE	1
Reihl, W; Sapira, JD; Scheib, ET; Shapiro, AP; Somani, S	1
Alpers, DH; Bartoscas, CS; Bixby, EM; Shih, VE; Thier, SO	1
Bar-Or, R; Cohen, BE; Jepson, JB; Pollak, S; Szeinberg, A	1
Asatoor, AM; Cheng, B; Edwards, KD; Lant, AF; Matthews, DM; Milne, MD; Navab, F; Richards, AJ	2
Bertaud, J; Lambertz, J; Paupe, J; Vialatte, J	1
Knapp, A	1
Berger, R; Broyer, M	1
Jepson, JB; Smith, HG; Smith, WR	1
Bissanti, A; Mainardi, L	1
Gershon, ES; Shader, RI	1
Martin, GM; Platter, H	1

Reviews

14 review(s) available for tryptophan and Amino Acid Transport Disorder, Neutral

Article	Year
[Hartnup disorder: Pathogenesis, pathophysiology, and therapy]. Nihon rinsho. Japanese journal of clinical medicine, 2006, Volume: 64 Suppl 2 Topics: Amino Acid Transport Systems, Neutral; Child; Cloning, Molecular; Genotype; Hartnup Disease; Humans; Infant; Infant, Newborn; Mutation; Niacinamide; Phenotype; Serotonin; Tryptophan	2006
Biochemistry of tryptophan in health and disease. Molecular aspects of medicine, 1983, Volume: 6, Issue:2 Topics: Animals; Appetite Regulation; Brain Chemistry; Depressive Disorder; Female; Hartnup Disease; Humans; Male; Malignant Carcinoid Syndrome; Pellagra; Pineal Gland; Rats; Schizophrenia; Serotonin; Sleep; Tryptophan; Tryptophan Hydroxylase; Tryptophan Oxygenase; Urinary Bladder Neoplasms	1983
[Hartnup syndrome. A rare metabolic disease]. Medizinische Monatsschrift fur Pharmazeuten, 1993, Volume: 16, Issue:6 Topics: Consanguinity; Hartnup Disease; Humans; Niacinamide; Tryptophan	1993
[Hartnup disease]. Ryoikibetsu shokogun shirizu, 1998, Issue:19 Pt 2 Topics: Amino Acids; Diagnosis, Differential; Hartnup Disease; Humans; Prognosis; Tryptophan	1998
[Nephrolithiasis and the gastrointestinal tract]. Zeitschrift fur Gastroenterologie. Verhandlungsband, 1979, Volume: 16 Topics: Amino Acids; Biological Transport; Calcium Oxalate; Cystinuria; Dehydration; Digestive System; Glutamine; Hartnup Disease; Humans; Kidney Calculi; Niacinamide; Oxalates; Solubility; Tryptophan	1979
[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
Niacin. Nutrition reviews, 1975, Volume: 33, Issue:10 Topics: Adolescent; Adult; Aged; Chemical Phenomena; Chemistry; Child; Child, Preschool; Dose-Response Relationship, Drug; Female; Hartnup Disease; Humans; Infant; Infant, Newborn; Leucine; Male; Middle Aged; Nicotinic Acids; Nutritional Requirements; Pellagra; Pregnancy; Tryptophan	1975
[Metabolism of tryptophan and its significance in pathology of childhood]. Pediatriia, 1972, Volume: 51, Issue:2 Topics: Child, Preschool; Cushing Syndrome; Diabetes Mellitus, Type 1; Down Syndrome; Female; Hartnup Disease; Hodgkin Disease; Humans; Infant; Pediatrics; Phenylketonurias; Tryptophan; Vitamin B 6 Deficiency	1972
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
[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
Disorders of intestinal transport of amino acids. American journal of diseases of children (1960), 1969, Volume: 117, Issue:1 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
[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
Transport of amino acids and peptides in the gut and the kidney. The Scientific basis of medicine annual reviews, 1971 Topics: Adult; Alanine; Amino Acids; Animals; Biological Transport, Active; Digestive System; Glycine; Hartnup Disease; Histidine; Humans; Hydrolysis; Intestinal Absorption; Kidney; Kidney Tubules; Leucine; Lysine; Methionine; Peptides; Phenylalanine; Proteins; Rats; Serine; Threonine; Tryptophan; Valine	1971

Other Studies

50 other study(ies) available for tryptophan and Amino Acid Transport Disorder, Neutral

Article	Year
The metabolic disorder in Hartnup disease. The Quarterly journal of medicine, 1960, Volume: 29 Topics: Ataxia; Hartnup Disease; Humans; Metabolic Diseases; Pellagra; Tryptophan	1960
Hartnup disease. Pediatrics, 1963, Volume: 31 Topics: Amino Acids; Hartnup Disease; Humans; Indoles; Metabolic Diseases; Niacin; Niacinamide; Pellagra; Proteins; Tryptophan	1963
Indole production in Hartnup disease. Lancet (London, England), 1963, Jan-19, Volume: 1, Issue:7273 Topics: Amino Acids; Ataxia; Hartnup Disease; Humans; Indoles; Pellagra; Tryptophan	1963
CLINICAL AND BIOCHEMICAL FEATURES OF A CASE OF HARTNUP DISEASE. British medical journal, 1964, Feb-01, Volume: 1, Issue:5378 Topics: Biochemical Phenomena; Biochemistry; Child; Genetics, Medical; Hartnup Disease; Humans; Indican; Indoleacetic Acids; Kidney; Kidney Diseases; Pellagra; Renal Aminoacidurias; Tryptophan; Urine	1964
[THE CLINICAL FORM OF HARTNUP'S DISEASE]. Acta paediatrica Belgica, 1963, Volume: 17 Topics: Diagnosis, Differential; Friedreich Ataxia; Hartnup Disease; Humans; Indican; Indoles; Infant; Metabolic Diseases; Niacin; Niacinamide; Pellagra; Tryptophan; Urine	1963
HARTNUP DISEASE IN TWO SIBLINGS. CLINICAL OBSERVATIONS AND BIOCHEMICAL STUDIES. Annales paediatriae Fenniae, 1964, Volume: 10 Topics: Adolescent; Ataxia; Child; Eczema; Genetics, Medical; Hartnup Disease; Humans; NAD; NADP; Niacin; Nicotinic Acids; Pellagra; Protein Deficiency; Renal Aminoacidurias; Siblings; Tryptophan	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
BIOCHEMICAL ASPECTS OF THE HARTNUP DISEASE. II. SOME OBSERVATIONS ON RATS ABOUT TRYPTOPHAN METABOLISM. Annales paediatrici. International review of pediatrics, 1964, Volume: 202 Topics: Child; Clinical Enzyme Tests; Hartnup Disease; Humans; Indican; Indoles; Kidney; Kynurenine; Metabolic Diseases; Neomycin; Niacin; Niacinamide; Nicotinic Acids; Nystatin; Pellagra; Rats; Renal Aminoacidurias; Tryptophan; Urine	1964
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
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
[METABOLIC DISORDERS IN POLYMORPHIC LIGHT DERMATOSES AND RECENT RESULTS OF INVESTIGATIONS IN CONNECTION WITH THE HARTNUP SYNDROME]. Archiv fur klinische und experimentelle Dermatologie, 1964, Jun-25, Volume: 219 Topics: Hartnup Disease; Humans; Indoles; Phenothiazines; Photosensitivity Disorders; Skin Diseases; Toxicology; Tryptophan; Urine	1964
Hartnup disease in psychiatric practice: clinical and biochemical features of three cases. Journal of neurology, neurosurgery, and psychiatry, 1960, Volume: 23 Topics: Hartnup Disease; Humans; Pellagra; Tryptophan	1960
A clinicobiochemical study of tryptophan and other plasma and urinary amino acids in the family with Hartnup disease. Advances in experimental medicine and biology, 2003, Volume: 527 Topics: Adolescent; Adult; Amino Acids; Child, Preschool; Female; Genes, Recessive; Hartnup Disease; Heterozygote; Homozygote; Humans; Hydroxyindoleacetic Acid; Male; Pedigree; Tryptophan	2003
Observations on nicotinic acid therapy in Hartnup disease. Archives of disease in childhood, 1967, Volume: 42, Issue:226 Topics: Hartnup Disease; Humans; Indican; Indoleacetic Acids; Kidney; Kynurenine; Nicotinic Acids; Renal Aminoacidurias; Tryptophan	1967
Treatment of Hartnup disease with nicotinic acid. Nutrition reviews, 1984, Volume: 42, Issue:7 Topics: Cerebellar Ataxia; Child; Female; Hartnup Disease; Humans; Male; Niacin; Niacinamide; Pellagra; Tryptophan	1984
Homozygosity mapping to chromosome 5p15 of a gene responsible for Hartnup disorder. Biochemical and biophysical research communications, 2001, Jun-08, Volume: 284, Issue:2 Topics: Child; Chromosome Mapping; Chromosomes, Human, Pair 4; Chromosomes, Human, Pair 5; Consanguinity; Female; Genes, Recessive; Genetic Linkage; Genetic Markers; Hartnup Disease; Homozygote; Humans; Japan; Lod Score; Male; Middle Aged; Pedigree; Tryptophan	2001
[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
Pellagra and mental disturbance. The Proceedings of the Nutrition Society, 1978, Volume: 37, Issue:2 Topics: Animals; Brain; Diet; Hartnup Disease; Humans; Mental Disorders; Nicotinic Acids; Pellagra; Pyridoxine; Rats; Schizophrenia; Tryptophan; Zea mays	1978
[Some hereditary disorders of intestinal resorption with renal dysfunction]. Der Internist, 1976, Volume: 17, Issue:7 Topics: Arginine; Child; Chlorides; Cystine; Cystinuria; Diarrhea; Female; Galactose; Glucose; Hartnup Disease; Humans; Infant, Newborn; Intestinal Absorption; Kidney Diseases; Lysine; Malabsorption Syndromes; Male; Pedigree; Tryptophan	1976
[Case of Hartnup's disease]. Klinicheskaia meditsina, 1977, Volume: 55, Issue:4 Topics: Adult; Female; Hartnup Disease; Humans; Serotonin; Tryptophan	1977
Hartnup disease. Clinical, pathological, and biochemical observations. Archives of neurology, 1976, Volume: 33, Issue:12 Topics: Adolescent; Adult; Amino Acids; Cerebellar Cortex; Cerebral Cortex; Cerebral Ventricles; Female; Geniculate Bodies; Hartnup Disease; Humans; Male; Muscles; Occipital Lobe; Pedigree; Purkinje Cells; Tryptophan	1976
[Letter: Permanent indicanuria. Heterozygote form of Hartnup's disease?]. La Nouvelle presse medicale, 1975, Mar-01, Volume: 4, Issue:9 Topics: Adult; Hartnup Disease; Heterozygote; Humans; Indican; Malabsorption Syndromes; Male; Pedigree; Tryptophan	1975
Tryptophan metabolism in nervous disease. Acta vitaminologica et enzymologica, 1975, Volume: 29, Issue:1-6 Topics: Acute Disease; Child; Hartnup Disease; Hepatolenticular Degeneration; Humans; Infant; Phenylketonurias; Porphyrias; Tryptophan	1975
Hartnup syndrome, progressive encephalopathy and allo-albuminaemia. A clinico-pathological case study. European journal of pediatrics, 1992, Volume: 151, Issue:12 Topics: Amino Acids; Blood Protein Disorders; Brain; Brain Chemistry; Child, Preschool; Female; Hartnup Disease; Humans; Serum Albumin; Tryptophan	1992
Tryptophan and its metabolites in a family with Hartnup disease. Advances in experimental medicine and biology, 1991, Volume: 294 Topics: Adolescent; Adult; Child; Female; Hartnup Disease; Humans; Hydroxyindoleacetic Acid; Intestinal Absorption; Kidney Tubules, Proximal; Kynurenine; Male; Tryptophan; Xanthurenates	1991
Use of ethyl esters of tryptophan to bypass the absorption defect in Hartnup disease. Nutrition reviews, 1990, Volume: 48, Issue:1 Topics: Dose-Response Relationship, Drug; Hartnup Disease; Humans; Tryptophan	1990
Circumvention of defective neutral amino acid transport in Hartnup disease using tryptophan ethyl ester. The Journal of clinical investigation, 1989, Volume: 84, Issue:1 Topics: Amino Acids; Animals; Biological Transport; Child, Preschool; Female; Hartnup Disease; Humans; Hydrolysis; Hydroxyindoleacetic Acid; Male; Niacinamide; Rats; Rats, Inbred Strains; Serotonin; Tryptophan	1989
[A case of Hartnup disease]. Nihon Hifuka Gakkai zasshi. The Japanese journal of dermatology, 1988, Volume: 98, Issue:1 Topics: Adult; Amino Acids; Female; Hartnup Disease; Humans; Niacinamide; Skin; Tryptophan	1988
[Association of celiac disease and Hartnup's disease? Value of the tryptophan loading test]. Gastroenterologie clinique et biologique, 1986, Volume: 10, Issue:2 Topics: Celiac Disease; Hartnup Disease; Humans; Male; Middle Aged; Tryptophan	1986
Tryptophan load and uptake of tryptophan by leukocytes in Hartnup disease. The Tohoku journal of experimental medicine, 1966, Volume: 90, Issue:4 Topics: Adolescent; Amino Acids; Chromatography, Paper; Female; Hartnup Disease; Humans; Indoleacetic Acids; Kynurenine; Leukocytes; Male; Niacinamide; Tryptophan	1966
Hartnup disease. The Tohoku journal of experimental medicine, 1967, Volume: 91, Issue:4 Topics: Adult; Amino Acids; Chromatography, Paper; Female; Hartnup Disease; Humans; Liver; Male; Niacinamide; Pedigree; Tryptophan	1967
[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
Indole metabolism in Hartnup disease. Advances in pharmacology, 1968, Volume: 6, Issue:Pt B Topics: Animals; Hartnup Disease; Humans; Indoles; Niacinamide; Rats; Tryptophan	1968
Hartnup disease. The Biochemical journal, 1969, Volume: 111, Issue:3 Topics: Child; Child, Preschool; Female; Hartnup Disease; Humans; Infant; Infant, Newborn; Male; Nervous System Diseases; Niacinamide; Renal Tubular Transport, Inborn Errors; Tryptophan; Vitamin B Deficiency	1969
Studies on intestinal absorption of amino acids and a dipeptide in a case of Hartnup disease. Gut, 1970, Volume: 11, Issue:5 Topics: Adult; Alanine; Amino Acids; Chromatography, Paper; Dipeptides; Female; Hartnup Disease; Histidine; Humans; Intestinal Absorption; Intestine, Small; Niacinamide; Phenylalanine; Radiography; Tryptophan	1970
[Tryptophan metabolism in patients with pellagra]. Archiv fur dermatologische Forschung, 1970, Volume: 240, Issue:1 Topics: Acetaminophen; Administration, Oral; Adult; Aged; Child, Preschool; Female; Hartnup Disease; Humans; Hydroxyindoleacetic Acid; Indoleacetic Acids; Kynurenine; Middle Aged; Niacinamide; Pellagra; Tryptamines; Tryptophan	1970
[Hartnup disease (author's transl)]. Monatsschrift fur Kinderheilkunde, 1973, Volume: 121, Issue:9 Topics: Adolescent; Amino Acids; Child; Feces; Female; Hartnup Disease; Hippurates; Histidine; Humans; Malabsorption Syndromes; Nicotinic Acids; Pyridoxine; Renal Aminoacidurias; Tryptophan; Tyrosine	1973
Transport of dibasic amino acids, cystine, and tryptophan by cultured human fibroblasts: absence of a defect in cystinuria and Hartnup disease. The Journal of clinical investigation, 1972, Volume: 51, Issue:8 Topics: Adult; Amino Acids; Arginine; Biological Transport; Cell Line; Cells, Cultured; Cystine; Cystinuria; Female; Fibroblasts; Hartnup Disease; Humans; Infant; Lysine; Male; Mutation; Skin; Tryptophan	1972
Some observations concerning mammalian indoxyl metabolism and its relationship to the formation of urinary indigo pigments. Metabolism: clinical and experimental, 1971, Volume: 20, Issue:5 Topics: Animals; Chromatography, Paper; Chromatography, Thin Layer; Diet; Female; Glucuronidase; Hartnup Disease; Humans; Indican; Indoles; Malabsorption Syndromes; Mass Spectrometry; Mineral Oil; Neomycin; Pyelonephritis; Rats; Sodium Chloride; Sunlight; Tryptophan	1971
Studies of intestinal transport defect in Hartnup disease. Gastroenterology, 1971, Volume: 61, Issue:4 Topics: Adolescent; Biological Transport; Carbon Isotopes; Child; Culture Techniques; Feces; Genes, Recessive; Hartnup Disease; Humans; Intellectual Disability; Intestinal Mucosa; Jejunum; Leucine; Lysine; Male; Methionine; Phenylalanine; Proline; Tryptophan	1971
Observations on urinary excretion of indolylacryloyl glycine. Clinica chimica acta; international journal of clinical chemistry, 1965, Volume: 11, Issue:6 Topics: Chromatography, Paper; Cross Infection; Escherichia coli; Genetics, Medical; Glycine; Hartnup Disease; Humans; In Vitro Techniques; Indoles; Intestines; Proteus; Tryptophan; Urine	1965
Intestinal absorption of two dipeptides in Hartnup disease. Gut, 1970, Volume: 11, Issue:5 Topics: Adult; Animals; Dipeptides; Female; Glycine; Hartnup Disease; Humans; Intestinal Absorption; Phenylalanine; Rats; Tryptophan	1970
Intestinal absorption of dipeptides and corresponding free amino acids in Hartnup disease. Clinical science, 1970, Volume: 39, Issue:1 Topics: Amino Acids; Animals; Dipeptides; Glycine; Hartnup Disease; Humans; Intestinal Absorption; Intestine, Small; Phenylalanine; Rats; Tryptophan	1970
[Pellagroid syndrome with pseudo-myopathic signs cured with pyridoxine]. Annales de pediatrie, 1970, Dec-02, Volume: 17, Issue:12 Topics: Child, Preschool; Diagnosis, Differential; Female; Hartnup Disease; Humans; Infant; Lupus Erythematosus, Systemic; Muscular Diseases; Neurologic Manifestations; Pellagra; Pyridoxine; Skin Manifestations; Tryptophan; Vitamin B 6 Deficiency	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
[Hartnup disease]. La Presse medicale, 1968, Jan-06, Volume: 76, Issue:1 Topics: Hartnup Disease; Humans; Indican; Renal Aminoacidurias; Tryptophan	1968
Interconversions of indolic acids by bacteria and rat tissue--possible relevance to Hartnup disorder. Clinical science, 1968, Volume: 34, Issue:2 Topics: Animals; Chromatography, Thin Layer; Electrophoresis; Hartnup Disease; Humans; Indoles; Injections, Intraperitoneal; Intestine, Small; Intubation, Gastrointestinal; Kidney; Liver; Male; Phenylketonurias; Rats; Tryptophan	1968
[Various current findings in the problem of pellagra]. Acta vitaminologica et enzymologica, 1968, Volume: 22, Issue:3 Topics: Alcoholism; Deficiency Diseases; Diet; Feeding Behavior; Hartnup Disease; Humans; Isoniazid; Isonicotinic Acids; Italy; Kynurenine; Mexico; Pellagra; Thiosemicarbazones; Tryptophan; United States; Zea mays	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
Tryptophane transport in cultures of human fibroblasts. Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.), 1966, Volume: 123, Issue:1 Topics: Biological Transport; Culture Techniques; Cystinuria; Fibroblasts; Hartnup Disease; Humans; Kinetics; Tryptophan	1966