Compounds > tryptophan

tryptophan and Ataxia

tryptophan has been researched along with Ataxia in 10 studies

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19905 (50.00)18.7374
1990's2 (20.00)18.2507
2000's2 (20.00)29.6817
2010's1 (10.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Berciano, J; Infante, J; Pelayo-Negro, AL; Rodríguez-Oroz, MC; Sánchez-Quintana, C; Tola-Arribas, MA; Volpini, V; Zeviani, M1
Ceuterick, C; De Jonghe, P; Dehaene, I; Dermaut, B; Löfgren, A; Martin, JJ; Moonen, M; Tack, P; Van Broeckhoven, C; Van Goethem, G; Van Zandijcke, M; Ververken, D; Wibail, A1
CRAWFORD, MA; GIRAO, CB; LOUGHRIDGE, LW; MILNE, MD1
ASATOOR, AM; CRASKE, J; LONDON, DR; MILNE, MD1
ARAKAWA, T; ITO, H; TADA, K; WADA, Y1
HJELT, L; LAHIKAINEN, T; OHMAN, S; VISAKORPI, JK1
Bentele, KH; Bürk, K; Habeck, M; Hellenbroich, Y; Kress, W; Schwinger, E; Unkelbach, S; Zühlke, C1
Yuki, N1
Chida, K; Okita, N; Tagawa, Y; Takase, S; Watanabe, S; Yuki, N1
Fumero, S; Monaco, F; Mondino, A; Mutani, R1

Other Studies

10 other study(ies) available for tryptophan and Ataxia

ArticleYear
Screening for POLG W748S and A467T mutations in ataxia patients from Spain.
    Movement disorders : official journal of the Movement Disorder Society, 2012, Sep-01, Volume: 27, Issue:10

    Topics: Adult; Age of Onset; Aged; Alanine; Ataxia; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Middle Aged; Mutation; Polymorphism, Single Nucleotide; Serine; Spain; Threonine; Tryptophan; Young Adult

2012
Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia.
    Neuromuscular disorders : NMD, 2003, Volume: 13, Issue:2

    Topics: Adolescent; Adult; Aged; Arginine; Ataxia; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Electron Transport Complex IV; Female; Genes, Recessive; Heterozygote; Humans; Magnetic Resonance Imaging; Male; Microscopy, Electron; Middle Aged; Molecular Sequence Data; Muscle, Skeletal; Mutation, Missense; Ophthalmoplegia, Chronic Progressive External; Pedigree; Succinate Dehydrogenase; Tryptophan

2003
The metabolic disorder in Hartnup disease.
    The Quarterly journal of medicine, 1960, Volume: 29

    Topics: Ataxia; Hartnup Disease; Humans; Metabolic Diseases; Pellagra; Tryptophan

1960
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
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
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
Aprataxin mutations are a rare cause of early onset ataxia in Germany.
    Journal of neurology, 2004, Volume: 251, Issue:5

    Topics: Ataxia; DNA Mutational Analysis; DNA-Binding Proteins; Exons; Female; Genetic Linkage; Genetic Variation; Germany; Haplotypes; Humans; Male; Microsatellite Repeats; Mutation; Nuclear Proteins; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Tryptophan

2004
Tryptophan-immobilized column adsorbs immunoglobulin G anti-GQ1b antibody from Fisher's syndrome: A new approach to treatment.
    Neurology, 1996, Volume: 46, Issue:6

    Topics: Adolescent; Adult; Aged; Ataxia; Autoantibodies; Autoimmune Diseases; Child; Chromatography, Affinity; Enzyme-Linked Immunosorbent Assay; Female; Gangliosides; Humans; Immunoglobulin G; Immunosorbent Techniques; Male; Middle Aged; Nervous System Diseases; Ophthalmoplegia; Plasmapheresis; Polyradiculoneuropathy; Polyvinyl Alcohol; Syndrome; Tryptophan

1996
[Immunoadsorption therapy for Fisher's syndrome: analysis of the recovery process of external ophthalmoplegia and the removal ability of anti-GQ1b antibodies].
    Rinsho shinkeigaku = Clinical neurology, 1996, Volume: 36, Issue:4

    Topics: Adult; Ataxia; Autoantibodies; Female; Gangliosides; Humans; Immunosorbent Techniques; Male; Middle Aged; Ophthalmoplegia; Reflex, Abnormal; Reflex, Stretch; Syndrome; Tryptophan

1996
Plasma and cerebrospinal fluid tryptophan in multiple sclerosis and degenerative diseases.
    Journal of neurology, neurosurgery, and psychiatry, 1979, Volume: 42, Issue:7

    Topics: Adult; Amino Acids; Ataxia; Female; Humans; Male; Middle Aged; Motor Neurons; Multiple Sclerosis; Neuromuscular Diseases; Tryptophan

1979