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List of works by Eugénie Mutez

A randomized, controlled, double-blind, crossover trial of zonisamide in myoclonus-dystonia

scientific article published on 6 April 2016

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study ⬇️

scientific article published on 30 August 2011

Independent and joint effects of the MAPT and SNCA genes in Parkinson disease

scientific article

Involvement of the immune system, endocytosis and EIF2 signaling in both genetically determined and sporadic forms of Parkinson's disease

scientific article published on 20 November 2013

LRRK2 detection in human biofluids: potential use as a Parkinson's disease biomarker?

scientific article published on February 2017

Large-scale assessment of polyglutamine repeat expansions in Parkinson disease

scientific article

Le traitement par apomorphine en perfusion continue sous-cutanée dans la maladie de Parkinson : analyse rétrospective d’une série de 81 patients

scholarly article by M. Rambour et al published March 2014 in Revue neurologique

Mini-Exome Coupled to Read-Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias

scientific article

Overexpression of Wild-Type Human Alpha-Synuclein Causes Metabolism Abnormalities in Thy1-aSYN Transgenic Mice

scientific article published on 02 October 2018

Parkinson disease: genetics and neuronal death

scientific article published on 01 April 2009

Parkinson's disease associated with 22q11.2 deletion: Clinical characteristics and response to treatment.

scientific article published on 28 April 2017

Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium

scientific article

Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants

scientific article published on 17 August 2013

RNA-binding disturbances as a continuum from spinocerebellar ataxia type 2 to Parkinson disease

scientific article published on 20 September 2016

SNCA locus duplication carriers: from genetics to Parkinson disease phenotypes.

scientific article published on 8 February 2011

Transcriptional profile of Parkinson blood mononuclear cells with LRRK2 mutation

scientific article published on 22 January 2010

Translation initiator EIF4G1 mutations in familial Parkinson disease

scientific article (publication date: 9 September 2011)

Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2.

scientific article

[Trichloroethylene intoxication presenting with temporal seizures]

scientific article published on 01 December 2006

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