Compounds > tryptophan

tryptophan and Aminoaciduria, Renal

tryptophan has been researched along with Aminoaciduria, Renal in 26 studies

Research

Studies (26)

TimeframeStudies, this research(%)All Research%
pre-199025 (96.15)18.7374
1990's1 (3.85)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
CHANG, LT; CHI, M1
SANECKA-OBACZ, M1
REDDY, V; SRIKANTIA, SG; VENKATACHALAM, PS1
BARNESS, LA; BESSELMAN, D; MELLMAN, WJ; TEDESCO, TA1
HJELT, L; LAHIKAINEN, T; OHMAN, S; VISAKORPI, JK1
CLODI, PH; DEUTSCH, E; NIEBAUER, G1
DELAEY, P; HOOFT, C; SNOECK, J; TIMMERMANS, J3
FOIS, A; LECCHINI, L2
MILNE, MD1
MURTAGH, JJ; RAPPALLINI, C1
CRAWFORD, MA1
VOLKOV, VP1
GROSS, JB; JONES, JD; MAHER, FT; ULRICH, JA1
Jones, PM; Lambert, AM; Pillai, PM; Wong, PW1
Engerman, RL; Kern, TS1
Bellet, H; Cheminal, R; Duran, M; Echenne, B1
Pratt, OE1
Antener, I; Bartelheimer, HK; Grüttner, R; Rybak, C1
Reed, WB1
Aviram, A; Gulyassy, PF; Peters, JH1
Ghosh, D; Green, R1
Berger, R; Broyer, M1
Scriver, CR; Whelan, DT1

Reviews

3 review(s) available for tryptophan and Aminoaciduria, Renal

ArticleYear
[RENAL TUBULAR DISEASES, WITH SPECIAL REFERENCE TO AMINOACIDURIA].
    Recenti progressi in medicina, 1964, Volume: 36

    Topics: Cystinosis; Cystinuria; Galactosemias; Genetics, Medical; Glycine; Hepatolenticular Degeneration; Humans; Kidney; Kidney Diseases; Kidney Tubules; Metabolic Diseases; Metabolism; Multiple Myeloma; Nephrotic Syndrome; Pellagra; Renal Aminoacidurias; Tryptophan; Urine

1964
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
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

Other Studies

23 other study(ies) available for tryptophan and Aminoaciduria, Renal

ArticleYear
AN INVESTIGATION INTO THE PROTEIN METABOLISM OF SCHIZOPHRENICS AND ITS CLINICAL SIGNIFICANCE.
    Chinese medical journal (Peking, China : 1932), 1963, Volume: 82

    Topics: China; Chromatography; Cysteine; Cystine; Indoles; Kidney; Proteins; Renal Aminoacidurias; Schizophrenia; Tryptophan

1963
[DETERMINATION OF TRYPTOPHAN IN THE URINE].
    Polski tygodnik lekarski (Warsaw, Poland : 1960), 1963, Jun-10, Volume: 18

    Topics: Chromatography; Kidney; Renal Aminoacidurias; Tryptophan; Urine

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
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
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
[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
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
[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
[SEROTONIN AND 5-HYDROXYINDOLACETIC ACID IN THE NEWBORN INFANT].
    Minerva pediatrica, 1964, Apr-28, Volume: 16

    Topics: Anemia; Anemia, Aplastic; Cardiovascular System; Gastrointestinal Tract; Humans; Hydroxyindoleacetic Acid; Indoleacetic Acids; Infant; Infant, Newborn; Infant, Newborn, Diseases; Metabolic Diseases; Metabolism; Nervous System; Pellagra; Phenylketonurias; Physiology; Renal Aminoacidurias; Respiratory System; Serotonin; Tryptophan

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
DEGRADATION OF AMINO-ACIDS IN THE LARGE GUT OF EAST AFRICANS AND ITS POSSIBLE SIGNIFICANCE.
    East African medical journal, 1964, Volume: 41

    Topics: Africa; Africa, Eastern; Amino Acids; Biomedical Research; Black People; Chromatography; Dopamine; Fruit; Humans; Hydroxyindoleacetic Acid; Indoleacetic Acids; Indoles; Intestinal Obstruction; Intestine, Large; Intestines; Proteins; Renal Aminoacidurias; Tetracycline; Tryptophan; Urine

1964
[FREE AMINO ACIDS IN THE BLOOD AND URINE OF PATIENTS WITH SOME FORMS OF DERMATOSIS].
    Vestnik dermatologii i venerologii, 1964, Volume: 38

    Topics: Alanine; Amino Acids; Arginine; Aspartic Acid; Blood; Cystine; Dermatitis; Eczema; Erythema Multiforme; Glutamates; Glycine; Histidine; Lupus Erythematosus, Systemic; Lysine; Proteins; Psoriasis; Renal Aminoacidurias; Serine; Skin Diseases; Taurine; Threonine; Toxicology; Tryptophan; Urticaria

1964
ENDOGENOUS RENAL CLEARANCES OF 12 INDIVIDUAL AMINO ACIDS IN FOUR APPARENTLY HEALTHY SUBJECTS AND IN FOUR AMINOACIDURIC PERSONS OF A KINDRED WITH HEREDITARY PANCREATITIS.
    The Journal of laboratory and clinical medicine, 1964, Volume: 63

    Topics: Amino Acids; Arginine; Biomedical Research; Cystine; Genetics, Medical; Glutamates; Healthy Volunteers; Histidine; Isoleucine; Kidney; Leucine; Lysine; Methionine; Pancreatitis; Pancreatitis, Chronic; Phenylalanine; Physiology; Renal Aminoacidurias; Threonine; Tryptophan; Tyrosine; Valine

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
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
Abnormal amino acid concentrations in plasma and urine of experimentally diabetic dogs.
    Research in experimental medicine. Zeitschrift fur die gesamte experimentelle Medizin einschliesslich experimenteller Chirurgie, 1983, Volume: 182, Issue:3

    Topics: Amino Acids; Amino Acids, Branched-Chain; Animals; Arginine; Diabetes Mellitus, Experimental; Dogs; Female; Glutamates; Glutamic Acid; Histidine; Male; Phenylalanine; Renal Aminoacidurias; Tryptophan; Tyrosine

1983
Congenital non-progressive encephalopathy and deafness with intermittent episodes of coma and hyperkynureninuria.
    Journal of inherited metabolic disease, 1996, Volume: 19, Issue:1

    Topics: Algeria; Brain Diseases; Child; Child, Preschool; Coma; Deafness; Female; Humans; Infant; Intellectual Disability; Kynurenine; Male; Pedigree; Renal Aminoacidurias; Tryptophan

1996
[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
Evaluation of amino acid and protein requirements in chronic uremia.
    Archives of internal medicine, 1970, Volume: 126, Issue:5

    Topics: Amino Acids; Biological Transport; Carbon Isotopes; Chronic Disease; Creatinine; Dietary Proteins; Glomerular Filtration Rate; Humans; Intestinal Absorption; Intestine, Small; Kidney Concentrating Ability; Nutritional Requirements; Proteins; Renal Aminoacidurias; Time Factors; Tryptophan; Uremia

1970
Urinary levels of kynurenine and 3-hydroxykynurenine in the rat: effects of triamterene.
    Biochemical and biophysical research communications, 1970, Dec-24, Volume: 41, Issue:6

    Topics: Amino Acids; Animals; Female; Injections, Intraperitoneal; Kynurenine; Metabolism; Mixed Function Oxygenases; Phenylbutyrates; Pteridines; Rats; Renal Aminoacidurias; Tetrahydrofolate Dehydrogenase; Triamterene; Tryptophan; Urination

1970
[Hartnup disease].
    La Presse medicale, 1968, Jan-06, Volume: 76, Issue:1

    Topics: Hartnup Disease; Humans; Indican; Renal Aminoacidurias; Tryptophan

1968
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