Compounds > histidine
Page last updated: 2024-08-17

histidine and Dystonia

histidine has been researched along with Dystonia in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's2 (40.00)29.6817
2010's1 (20.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
Barone, P; Cicarelli, G; Cuoco, S; Gagliardi, M; Pellecchia, MT; Procopio, R; Quattrone, A; Russillo, MC; Scarpa, A; Sorrentino, C; Talarico, M; Vinciguerra, C1
Borggraefe, I; Fischer, H; Garavaglia, B; Gasser, T; Grundmann, K; Kamm, C; Klein, C; Kullmann, S; Kupsch, A; Lobsien, E; Nardocci, N; Schrader, C; Sharma, M1
Bahman, I; Bhatia, KP; Brüggemann, N; Erogullari, A; Kaiser, FJ; Klein, C; Lohmann, K; Najmabadi, H; Osmanovic, A; Ramirez, A; Schneider, SA; Shafa, MA; Shafiee, K; Winkler, S1
Antonozzi, I; Carducci, C; Criscuolo, C; De Michele, G; De Rosa, A; Filla, A; Giovanniello, T; Menchise, V; Striano, S; Xhoxhi, E1
Hirano, M; Imai, T; Ito, H; Matsumoto, S; Tamaru, Y; Ueno, S1

Other Studies

5 other study(ies) available for histidine and Dystonia

ArticleYear
A novel phenotype in an Italian family with a rare progranulin mutation.
    Journal of neurology, 2022, Volume: 269, Issue:11

    Topics: Arginine; Dysphonia; Dystonia; Frontotemporal Dementia; Histidine; Humans; Intercellular Signaling Peptides and Proteins; Mutation; Phenotype; Progranulins; Respiratory Sounds

2022
Susceptibility to DYT1 dystonia in European patients is modified by the D216H polymorphism.
    Neurology, 2008, Jun-03, Volume: 70, Issue:23

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Aspartic Acid; Child; Dystonia; Genetic Predisposition to Disease; Histidine; Humans; Middle Aged; Molecular Chaperones; Polymorphism, Single Nucleotide; White People

2008
Homozygous THAP1 mutations as cause of early-onset generalized dystonia.
    Movement disorders : official journal of the Movement Disorder Society, 2011, Volume: 26, Issue:5

    Topics: Adult; Apoptosis Regulatory Proteins; Carcinoma; Cell Line, Tumor; Consanguinity; DNA-Binding Proteins; Dystonia; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Histidine; Homozygote; Humans; Iran; Leucine; Male; Middle Aged; Mutation; Nuclear Proteins; Pedigree

2011
A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia.
    Journal of neurology, 2007, Volume: 254, Issue:8

    Topics: Adolescent; Dihydroxyphenylalanine; DNA Mutational Analysis; Dopamine Agents; Dystonia; Family Health; Female; Glutamine; GTP Cyclohydrolase; Histidine; Humans; Mutation

2007
Mutant GTP cyclohydrolase I mRNA levels contribute to dopa-responsive dystonia onset.
    Annals of neurology, 1996, Volume: 40, Issue:5

    Topics: Adult; Amino Acid Sequence; Base Sequence; Circadian Rhythm; Dystonia; Exons; Female; GTP Cyclohydrolase; Histidine; Humans; Introns; Japan; Levodopa; Male; Nuclear Family; Point Mutation; Polymerase Chain Reaction; Proline; RNA, Messenger

1996