Compounds > histidine
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histidine and Adult-Onset Dystonias

histidine has been researched along with Adult-Onset Dystonias in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's3 (60.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Alechine, E; Caputo, M; Corach, D; Irisarri, M; Micheli, FE; Pellene, LA; Perandones, C; Roca, CU1
Blanchard, A; Brice, A; Calender, A; Cif, L; Claustres, M; Clot, F; Collod-Beroud, G; Dhaenens, CM; Dürr, A; Frédéric, MY; Lesca, G; Martinez, M; Molinari, N; Sablonniere, B; Tuffery-Giraud, S; Vidailhet, M1
Herzfeld, T; Korinthenberg, R; Müller, U1
Burgunder, JM; Chen, Y; Huang, R; Shang, HF; Song, W1
Amouri, R; Driss, A; Hentati, F; Kefi, M; Murayama, K; Nishino, I1

Other Studies

5 other study(ies) available for histidine and Adult-Onset Dystonias

ArticleYear
Analysis of D216H polymorphism in Argentinean patients with primary dystonia.
    Journal of neurogenetics, 2013, Volume: 27, Issue:1-2

    Topics: Adolescent; Adult; Age of Onset; Argentina; Aspartic Acid; Child; Dystonic Disorders; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Histidine; Humans; Male; Middle Aged; Molecular Chaperones; Polymorphism, Single Nucleotide; Young Adult

2013
The p.Asp216His TOR1A allele effect is not found in the French population.
    Movement disorders : official journal of the Movement Disorder Society, 2009, Apr-30, Volume: 24, Issue:6

    Topics: Alleles; Aspartic Acid; DNA Mutational Analysis; Dystonic Disorders; France; Gene Frequency; Histidine; Humans; Molecular Chaperones; Polymorphism, Single Nucleotide

2009
D216H polymorphism within TOR1A does not affect penetrance in DRD and is not a general modifier in primary dystonia.
    Movement disorders : official journal of the Movement Disorder Society, 2011, Volume: 26, Issue:1

    Topics: Aspartic Acid; Dystonic Disorders; Family Health; Female; Gene Frequency; Histidine; Humans; Male; Molecular Chaperones; Penetrance; Polymorphism, Genetic

2011
Assessment of D216H DYT1 polymorphism in a Chinese primary dystonia patient cohort.
    European journal of neurology, 2012, Volume: 19, Issue:6

    Topics: Adult; Aged; Asian People; Asparagine; Dystonic Disorders; Female; Follow-Up Studies; Genetic Association Studies; Genetic Predisposition to Disease; Histidine; Humans; Male; Middle Aged; Molecular Chaperones; Polymorphism, Single Nucleotide; Young Adult

2012
Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy.
    Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:5

    Topics: Adult; DNA Mutational Analysis; Dystonic Disorders; Extremities; Family Health; Female; Histidine; Humans; Leucine; Male; Methionine; Middle Aged; Multienzyme Complexes; Muscle, Skeletal; Mutation; Myositis, Inclusion Body; Staining and Labeling; Threonine; Tunisia

2005