Compounds > tryptophan

tryptophan and Cerebellar Ataxia

tryptophan has been researched along with Cerebellar Ataxia in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19905 (62.50)18.7374
1990's2 (25.00)18.2507
2000's1 (12.50)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
FOIS, A; LECCHINI, L1
Fenton, DA; Toseland, PA; Wilkinson, JD1
Deguchi, K; Takahashi, N; Takeuchi, H; Yuki, N1
Ichikawa, H; Kawamura, M; Sugita, K; Suzuki, M; Watanabe, Y; Yuki, N1
Ase, AR; Lalonde, R; Le Marec, N; Reader, TA1
Forman, P; Justice, P; Tabahoff, B; Wong, PW1
Bender, DA; McCreanor, GM; Salih, MA1

Other Studies

8 other study(ies) available for tryptophan and Cerebellar Ataxia

ArticleYear
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
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
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
[Immunoadsorption therapy on Fisher's syndrome--removal ability of anti-ganglioside antibodies by tryptophan-linked immunoadsorbent].
    Rinsho shinkeigaku = Clinical neurology, 1995, Volume: 35, Issue:8

    Topics: Adult; Autoantibodies; Cerebellar Ataxia; Female; Gangliosides; Gels; Humans; Immunosorbent Techniques; Ophthalmoplegia; Phenylalanine; Polyvinyl Alcohol; Reflex, Abnormal; Reflex, Stretch; Syndrome; Tryptophan

1995
[Removal ability of IgG anti-GQ1b antibody in immunoadsorption therapy for Fisher syndrome--comparison of the removal ability between tryptophane column and phenylalanine column].
    Rinsho shinkeigaku = Clinical neurology, 1996, Volume: 36, Issue:2

    Topics: Adult; Autoantibodies; Cerebellar Ataxia; Female; Gangliosides; Humans; Immunoglobulin G; Immunosorbent Techniques; Ophthalmoplegia; Phenylalanine; Polyradiculoneuropathy; Reflex, Abnormal; Syndrome; Tryptophan

1996
Differential effects of L-trytophan and buspirone on biogenic amine contents and metabolism in Lurcher mice cerebellum.
    Neuroscience letters, 2000, Feb-25, Volume: 280, Issue:3

    Topics: 3,4-Dihydroxyphenylacetic Acid; Animals; Biogenic Amines; Buspirone; Cerebellar Ataxia; Cerebellum; Disease Models, Animal; Dopamine; Female; Heterozygote; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Mice; Mice, Neurologic Mutants; Norepinephrine; Serotonin; Tryptophan

2000
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
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