Lista de obras -

Analysis of COQ2 gene in multiple system atrophy

artículo científico publicado en 2014

Analysis of nuclear export sequence regions of FUS-Related RNA-binding proteins in essential tremor

artículo científico publicado en 2014

Association study between multiple system atrophy and TREM2 p.R47H

Cerebellar ataxia in progressive supranuclear palsy: An autopsy study of PSP-C.

artículo científico publicado en 2016

EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population

artículo científico publicado en 2014

Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus

artículo científico publicado en 2015

Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease

artículo científico publicado en 2014

Heterozygous PINK1 p.G411S increases risk of Parkinson's disease via a dominant-negative mechanism

artículo científico publicado en 2016

Investigating FUS variation in Parkinson's disease

artículo científico

LRRK2 exonic variants and risk of multiple system atrophy

artículo científico publicado en 2014

MAPT haplotype diversity in multiple system atrophy

artículo científico publicado en 2016

Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders

artículo científico publicado en 2015

Multiple system atrophy and apolipoprotein E.

artículo científico publicado en 2018

Rapid screening of ATP13A2 variant with high-resolution melting analysis

artículo científico publicado en 2010

Reply: Heterozygous PINK1 p.G411S in rapid eye movement sleep behaviour disorder

artículo científico publicado en 2017

Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies

artículo científico publicado en 2015

Structural and Functional Impact of Parkinson Disease-Associated Mutations in the E3 Ubiquitin Ligase Parkin

artículo científico publicado en 2015

TREM2 p.R47H substitution is not associated with dementia with Lewy bodies

artículo científico publicado en 2016

Three sib-pairs of autopsy-confirmed progressive supranuclear palsy

artículo científico publicado en 2014

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

artículo científico

Lista de obras de

Analysis of COQ2 gene in multiple system atrophy

Analysis of nuclear export sequence regions of FUS-Related RNA-binding proteins in essential tremor

Association study between multiple system atrophy and TREM2 p.R47H

Cerebellar ataxia in progressive supranuclear palsy: An autopsy study of PSP-C.

EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population

Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus

Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease

Heterozygous PINK1 p.G411S increases risk of Parkinson's disease via a dominant-negative mechanism

Investigating FUS variation in Parkinson's disease

LRRK2 exonic variants and risk of multiple system atrophy

MAPT haplotype diversity in multiple system atrophy

Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders

Multiple system atrophy and apolipoprotein E.

Rapid screening of ATP13A2 variant with high-resolution melting analysis

Reply: Heterozygous PINK1 p.G411S in rapid eye movement sleep behaviour disorder

Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies

Structural and Functional Impact of Parkinson Disease-Associated Mutations in the E3 Ubiquitin Ligase Parkin

TREM2 p.R47H substitution is not associated with dementia with Lewy bodies

Three sib-pairs of autopsy-confirmed progressive supranuclear palsy

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