List of works - Emmanuel Broussolle - Paulina

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List of works by Emmanuel Broussolle

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A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

scientific article

How much phenotypic variation can be attributed to parkin genotype?

scientific article

Bilateral pallidal deep brain stimulation for the treatment of patients with dystonia-choreoathetosis cerebral palsy: a prospective pilot study

scientific article

C9orf72 repeat expansions are a rare genetic cause of parkinsonism

scientific article

Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study

scientific article

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

scientific article

LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans

scientific article published on March 2007

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

scientific article published on 17 July 2009

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

scientific article published in May 2003

Subthalamic stimulation and neuropsychiatric symptoms in Parkinson's disease: results from a long-term follow-up cohort study

scientific article published on 7 February 2018

Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes

scientific article published on 26 February 2018

Spinocerebellar ataxia with sensory neuropathy (SCA25)

Historical crossroads in the conceptual delineation of apathy in Parkinson's disease

scientific article published on 9 January 2018