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Publications by Alexis Brice
Mutation Analysis of Consanguineous Moroccan Patients With Parkinson’s Disease Combining Microarray and Gene Panel
Frontiers in Neurology
Neurology
SCA15 Due to Large ITPR1 Deletions in a Cohort of 333 White Families With Dominant Ataxia
Archives of Neurology
Automated Classification of Neurodegenerative Parkinsonian Syndromes Using Multimodal Magnetic Resonance Imaging in a Clinical Setting
Differences in the Presentation and Progression of Parkinson's Disease by Sex
A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-Q34
American Journal of Human Genetics
Genetics
Origin of the Mutations in the Parkin Gene in Europe: Exon Rearrangements Are Independent Recurrent Events, Whereas Point Mutations May Result From Founder Effects
American Journal of Human Genetics
Genetics
Hereditary Spastic Paraplegia SPG13 Is Associated With a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60
American Journal of Human Genetics
Genetics
Use of Haplotype Information to Test Involvement of the LRP Gene in Alzheimer's Disease in the French Population
European Journal of Human Genetics
Genetics
Juvenile-Onset Parkinsonism as a Result of the First Mutation in the Adenosine Triphosphate Orientation Domain of PINK1
Archives of Neurology
Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene
Archives of Neurology
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