α-synuclein locus duplication as a cause of familial Parkinson's disease

…, L Defebvre, P Amouyel, M Farrer, A Destée - The Lancet, 2004 - thelancet.com
Genomic triplication of the α-synuclein gene (SNCA) has been reported to cause hereditary
early-onset parkinsonism with dementia. These findings prompted us to screen for …

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

…, B Pillon, C Ardouin, Y Agid, A Destée… - … England Journal of …, 2005 - Mass Medical Soc
Background Severe forms of dystonia respond poorly to medical treatment. Deep-brain
stimulation is a reversible neurosurgical procedure that has been used for the treatment of …

Targeting chelatable iron as a therapeutic modality in Parkinson's disease

…, I Strubi-Vuillaume, N Zahr, A Destée… - Antioxidants & redox …, 2014 - liebertpub.com
Aims: The pathophysiological role of iron in Parkinson's disease (PD) was assessed by a
chelation strategy aimed at reducing oxidative damage associated with regional iron …

The Lille apathy rating scale (LARS), a new instrument for detecting and quantifying apathy: validation in Parkinson's disease

…, K Dujardin, D Devos, C Denève, A Destée… - Journal of Neurology …, 2006 - jnnp.bmj.com
Background: Apathy is usually defined as reduced interest and participation in various activities.
It is a frequent consequence of neurological and psychiatric disorders. Although various …

Memantine for patients with Parkinson's disease dementia or dementia with Lewy bodies: a randomised, double-blind, placebo-controlled trial

M Emre, M Tsolaki, U Bonuccelli, A Destée… - The Lancet …, 2010 - thelancet.com
Background Previous studies have suggested that patients with Lewy-body-related dementias
might benefit from treatment with the N-methyl D-aspartate receptor antagonist memantine…

[PDF][PDF] Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy

…, A Durr, JF Deleuze, M Tazir, A Destée… - The American Journal of …, 2016 - cell.com
Autosomal-recessive early-onset parkinsonism is clinically and genetically heterogeneous.
The genetic causes of approximately 50% of autosomal-recessive early-onset forms of …

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

…, K Dujardin, V Hahn-Barma, Y Agid, A Destée… - The Lancet …, 2007 - thelancet.com
Background We have previously reported the efficacy and safety of bilateral pallidal stimulation
for primary generalised dystonia in a prospective, controlled, multicentre study with 1 …

STN-DBS frequency effects on freezing of gait in advanced Parkinson disease

C Moreau, L Defebvre, A Destée, S Bleuse, F Clement… - Neurology, 2008 - AAN Enterprises
Background: Severe gait disturbances and freezing episodes (frequently resistant to optimal
dopaminergic treatment) often appear in advanced Parkinson disease (PD). Even several …

[PDF][PDF] Translation initiator EIF4G1 mutations in familial Parkinson disease

…, RA Gibson, F Hentati, DW Dickson, A Destée… - The American Journal of …, 2011 - cell.com
Genome-wide analysis of a multi-incident family with autosomal-dominant parkinsonism has
implicated a locus on chromosomal region 3q26-q28. Linkage and disease segregation is …

Characteristics of apathy in Parkinson's disease

…, M Delliaux, P Krystkowiak, A Destée… - Movement …, 2007 - Wiley Online Library
The objective of this study was to use the Lille Apathy Rating Scale to assess apathy in a
large population of Parkinson's disease (PD) patients and identify several different apathy …