Lista de obras -

A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations

artículo científico publicado en 2008

A multidisciplinary study of patients with early-onset PD with and without parkin mutations

artículo científico publicado en 2008

A multitracer dopaminergic PET study of young-onset parkinsonian patients with and without parkin gene mutations.

artículo científico publicado en 2009

Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease

artículo científico publicado en 2004

Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms

artículo científico publicado en 2009

EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants? ⬇️

artículo científico publicado el 1 de junio de 2012

Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease

artículo científico publicado en 2007

G2019S LRRK2 mutation in French and North African families with Parkinson's disease

artículo científico publicado en 2005

G51D α‐synuclein mutation causes a novel Parkinsonian–pyramidal syndrome ⬇️

artículo científico publicado el 1 de abril de 2013

Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population

artículo científico publicado en 2010

How much phenotypic variation can be attributed to parkin genotype?

artículo científico publicado en 2003

Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

artículo científico publicado en 2008

LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans

artículo científico publicado en 2007

LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century

artículo científico publicado en 2005

Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease

artículo científico publicado en 2010

Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease

artículo científico publicado en 2009

New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism ⬇️

artículo científico publicado el 22 de abril de 2003

Parkin mutations are frequent in patients with isolated early-onset parkinsonism

artículo científico publicado en 2003

Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans

artículo científico publicado en 2010

The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism

artículo científico publicado en 2013

Young-onset Parkinson disease with and without parkin gene mutations: a fluorodopa F 18 positron emission tomography study

artículo científico publicado en 2003

Lista de obras de

A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations

A multidisciplinary study of patients with early-onset PD with and without parkin mutations

A multitracer dopaminergic PET study of young-onset parkinsonian patients with and without parkin gene mutations.

Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease

Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms

EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants? ⬇️

Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease

G2019S LRRK2 mutation in French and North African families with Parkinson's disease

G51D α‐synuclein mutation causes a novel Parkinsonian–pyramidal syndrome ⬇️

Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population

How much phenotypic variation can be attributed to parkin genotype?

Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans

LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century

Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease

Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease

New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism ⬇️

Parkin mutations are frequent in patients with isolated early-onset parkinsonism

Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans

The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism

Young-onset Parkinson disease with and without parkin gene mutations: a fluorodopa F 18 positron emission tomography study