Association of the COQ2 V393A variant with risk of multiple system atrophy in East Asians: a case–control study and meta-analysis of the literature

COQ2gene variants associate with cerebellar subtype of multiple system atrophy in Chinese

(2015) Chin-Hsien Lin et al.   MOVEMENT DISORDERS

Mutation scanning of the COQ2 gene in ethnic Chinese patients with multiple-system atrophy

(2015) Yong Ping Chen et al.   NEUROBIOLOGY OF AGING

COQ2 p.V393A variant, rs148156462, is not associated with Parkinson's disease in a Taiwanese population

(2015) Chin-Hsien Lin et al.   NEUROBIOLOGY OF AGING

Analysis of COQ2 gene in multiple system atrophy

(2014) Kotaro Ogaki et al.   Molecular Neurodegeneration

Neuropathology of multiple system atrophy: New thoughts about pathogenesis

(2014) Kurt A. Jellinger   MOVEMENT DISORDERS

Mutant COQ2 in Multiple-System Atrophy

(2014)   NEW ENGLAND JOURNAL OF MEDICINE

Mutations in COQ2 in Familial and Sporadic Multiple-System Atrophy

(2013)   NEW ENGLAND JOURNAL OF MEDICINE

Update on novel familial forms of Parkinson's disease and multiple system atrophy

(2013) Shinsuke Fujioka et al.   PARKINSONISM & RELATED DISORDERS

Neuropathology underlying clinical variability in patients with synucleinopathies

(2011) Glenda M. Halliday et al.   ACTA NEUROPATHOLOGICA

Diagnostic criteria for multiple system atrophy and progressive supranuclear palsy

(2010) G.K. Wenning et al.   REVUE NEUROLOGIQUE

Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency

(2008) Catarina M. Quinzii et al.   FASEB JOURNAL

Associations between multiple system atrophy and polymorphisms ofSLC1A4,SQSTM1, andEIF4EBP1Genes

(2008) Hiroyuki Soma et al.   MOVEMENT DISORDERS

Second consensus statement on the diagnosis of multiple system atrophy

(2008) S. Gilman et al.   NEUROLOGY