Search filters

List of works by Alain Destée

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

scientific article published in January 2009

Bilateral deep-brain stimulation of the globus pallidus in primary generalized dystonia

scientific article

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

scientific article

Bilateral, pallidal, deep-brain stimulation in primary generalised dystonia: a prospective 3 year follow-up study

scientific article published in March 2007

Effects of pulse width variations in pallidal stimulation for primary generalized dystonia

scientific article published on 29 June 2007

How much phenotypic variation can be attributed to parkin genotype?

scientific article

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 exon 41 mutations in sporadic Parkinson disease in Europeans

scientific article published on March 2007

Linkage exclusion in French families with probable Parkinson's disease

article

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

scientific journal article

Methylphenidate for gait hypokinesia and freezing in patients with Parkinson's disease undergoing subthalamic stimulation: a multicentre, parallel, randomised, placebo-controlled trial

scientific article

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

scientific article published on 02 October 2018

Polymorphism of the dopamine transporter type 1 gene modifies the treatment response in Parkinson's disease

scientific article published on 23 March 2015

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

Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease

scientific article published on 22 July 2011

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

scientific article published on 8 February 2011

Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy

scientific article

TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment

scientific article

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)

Paulina is supported by:

About Paulina

Help