Compounds > tryptophan

tryptophan and Friedreich Disease

tryptophan has been researched along with Friedreich Disease in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19905 (71.43)18.7374
1990's0 (0.00)18.2507
2000's1 (14.29)29.6817
2010's1 (14.29)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
De Smet, S; Foury, F; Leidgens, S1
DEMEULEMEESTER, F1
DELAEY, P; HOOFT, C; SNOECK, J; TIMMERMANS, J1
FISCHL, J; RABIAH, S1
FOIS, A; LECCHINI, L1
Botez, MI; Young, SN1
Curzon, G; Robinson, N; Theaker, P1

Other Studies

7 other study(ies) available for tryptophan and Friedreich Disease

ArticleYear
Frataxin interacts with Isu1 through a conserved tryptophan in its beta-sheet.
    Human molecular genetics, 2010, Jan-15, Volume: 19, Issue:2

    Topics: Amino Acid Sequence; Conserved Sequence; Frataxin; Friedreich Ataxia; Humans; Iron-Binding Proteins; Mitochondrial Proteins; Models, Biological; Molecular Conformation; Molecular Sequence Data; Protein Binding; Protein Structure, Secondary; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Sequence Alignment; Tryptophan

2010
[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
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
DETERMINATION OF FREE AND TOTAL INDOLE-3-ACETIC ACID AND OF THE INDOLE INDEX.
    Clinical chemistry, 1964, Volume: 10

    Topics: Friedreich Ataxia; Humans; Indoleacetic Acids; Indoles; Intestines; Kynurenine; Metabolism; Myotonia; Phenylketonurias; Poisoning; Research; Schizophrenia; 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
Biogenic amine metabolites and thiamine in cerebrospinal fluid in heredo-degenerative ataxias.
    The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, 2001, Volume: 28, Issue:2

    Topics: Adult; Aged; Female; Friedreich Ataxia; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Magnetic Resonance Imaging; Male; Methoxyhydroxyphenylglycol; Middle Aged; Olivopontocerebellar Atrophies; Severity of Illness Index; Thiamine; Tomography, Emission-Computed, Single-Photon; Tomography, X-Ray Computed; Tryptophan

2001
Excretion of tryptophan metabolites in Friedreich's ataxia.
    Journal of clinical pathology, 1965, Volume: 18, Issue:6

    Topics: Friedreich Ataxia; Humans; Hydroxyindoleacetic Acid; Indoleacetic Acids; Kynurenine; Tryptophan; Urine

1965