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Annales De Cardiologie Et D'Angeiologie|September 1, 1991
[Effects on the bone metabolism of long-term treatment with antivitamins K1]T Van der Linden, E Houvenagel, P Graux, et al.Neuromuscular Disorders : NMD|September 1, 1993
Merrf family with 8344 mutation in tRNA (lys). Evidence of a mitochondrial vasculopathy in muscle biopsiesM Coquet, F Degoul, A Vital, et al.Revue Neurologique|April 9, 2002
[Validation of the French language version of the Parkinson's Disease Questionnaire - PDQ-39]P Auquier, C Sapin, M Ziegler, et al.Revue Neurologique|June 12, 2012
Validation of the French version of the MSA health-related Quality of Life scale (MSA-QoL)W G Meissner, A Foubert-Samier, S Dupouy, et al.Neurology|September 30, 2010
Motor activation in multiple system atrophy and Parkinson disease: a PET studyP Payoux, C Brefel-Courbon, F Ory-Magne, et al.Journal of Medical Genetics|April 10, 2009
Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's diseaseS Lesage, C Condroyer, A Lannuzel, et al.Revue Neurologique|June 20, 2016
French consensus procedure for assessing cognitive function in Parkinson's diseaseK Dujardin, N Auzou, E Lhommée, et al.American Journal of Human Genetics|January 23, 1999
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxiaA Ducros, C Denier, A Joutel, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 16, 2015
New insights into orthostatic hypotension in multiple system atrophy: a European multicentre cohort studyA Pavy-Le Traon, A Piedvache, S Perez-Lloret, et al.Annals of Neurology|January 5, 2002
McLeod neuroacanthocytosis: genotype and phenotypeA Danek, J P Rubio, L Rampoldi, et al.Pageof 11