enkephalin, leucine and Cerebellar Ataxia

enkephalin, leucine has been researched along with Cerebellar Ataxia in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	2 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bakalkin, G; Bertrand, P; Brice, A; Durr, A; Fokkens, MR; Goas, JY; Jezierska, J; Kok, J; Robin, C; Stevanin, G; Verbeek, DS; Watanabe, H; Zagnoli, F	1
Chan, S; Coppola, G; Fogel, BL; Geschwind, DH; Huang, A; Klein, E; Lane, J; Lee, JY; Mamah, C; Osborn, GE; Perlman, S; Wahnich, A	1

Other Studies

2 other study(ies) available for enkephalin, leucine and Cerebellar Ataxia

Article	Year
Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia cases. Journal of neurology, 2013, Volume: 260, Issue:7 Topics: Adolescent; Adult; Age of Onset; Cerebellar Ataxia; Enkephalins; Female; Genetic Linkage; Heterozygote; Humans; Male; Middle Aged; Mutation; Pedigree; Protein Precursors	2013
Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia. Movement disorders : official journal of the Movement Disorder Society, 2012, Volume: 27, Issue:3 Topics: Adult; Aged; Cerebellar Ataxia; Cytoskeletal Proteins; Databases, Bibliographic; DNA Helicases; Enkephalins; Female; Genetic Predisposition to Disease; Genetic Testing; Heat-Shock Proteins; Humans; Lamin Type B; Magnetic Resonance Imaging; Male; Middle Aged; Multifunctional Enzymes; Mutation; Nerve Tissue Proteins; Nuclear Proteins; Phenotype; Protein Precursors; RNA Helicases; Transglutaminases	2012

Article

Year

Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia cases.

Journal of neurology, 2013, Volume: 260, Issue:7

Topics: Adolescent; Adult; Age of Onset; Cerebellar Ataxia; Enkephalins; Female; Genetic Linkage; Heterozygote; Humans; Male; Middle Aged; Mutation; Pedigree; Protein Precursors

2013

Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia.

Movement disorders : official journal of the Movement Disorder Society, 2012, Volume: 27, Issue:3

Topics: Adult; Aged; Cerebellar Ataxia; Cytoskeletal Proteins; Databases, Bibliographic; DNA Helicases; Enkephalins; Female; Genetic Predisposition to Disease; Genetic Testing; Heat-Shock Proteins; Humans; Lamin Type B; Magnetic Resonance Imaging; Male; Middle Aged; Multifunctional Enzymes; Mutation; Nerve Tissue Proteins; Nuclear Proteins; Phenotype; Protein Precursors; RNA Helicases; Transglutaminases

2012