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

histidine and Parkinsonian Disorders

histidine has been researched along with Parkinsonian Disorders in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Funayama, M; Hattori, N; Li, Y; Matsuura, E; Nishioka, K; Takanashi, M; Takashima, H; Tsuyama, S; Yoshino, H1
Bonifati, V; Farrer, MJ; Ferreira, JJ; Griffith, A; Haugarvoll, K; Kachergus, J; Latsoudis, H; Lin, CH; Plaitakis, A; Ross, OA; Sampaio, C; Spanaki, C; Wu, RM; Zabetian, CP1
Birk Møller, L; Diepold, K; Güttler, F; Hougaard, P; Romstad, A; Rostasy, K; Schütz, B; Wilken, B1

Other Studies

3 other study(ies) available for histidine and Parkinsonian Disorders

ArticleYear
Isolated nigral degeneration without pathological protein aggregation in autopsied brains with LRRK2 p.R1441H homozygous and heterozygous mutations.
    Acta neuropathologica communications, 2018, 10-17, Volume: 6, Issue:1

    Topics: Aged; alpha-Synuclein; Astrocytes; Autopsy; DNA-Binding Proteins; Female; Gene Expression Regulation; Histidine; Homozygote; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Mutation; Neurodegenerative Diseases; Parkinsonian Disorders; Proline; Protein Aggregation, Pathological; Substantia Nigra; tau Proteins

2018
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.
    Parkinsonism & related disorders, 2009, Volume: 15, Issue:6

    Topics: Adult; Arginine; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Haplotypes; Histidine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Parkinsonian Disorders; Polymorphism, Single Nucleotide; Protein Serine-Threonine Kinases

2009
Levodopa-responsive infantile parkinsonism due to a novel mutation in the tyrosine hydroxylase gene and exacerbation by viral infections.
    Movement disorders : official journal of the Movement Disorder Society, 2005, Volume: 20, Issue:6

    Topics: Animals; Antiparkinson Agents; Central Nervous System Viral Diseases; Child, Preschool; DNA Mutational Analysis; Female; Histidine; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Levodopa; Mice; Mutation; Parkinsonian Disorders; Rats; Treatment Outcome; Tyrosine; Tyrosine 3-Monooxygenase

2005