Search results for: Rafaëlle Bernard
Clinical Genetics > 106 > 1 > 13 - 26
Orphanet Journal of Rare Diseases > 2018 > 13 > 1 > 1-10
Human Mutation > 38 > 10 > 1432 - 1441
BMC Medical Genetics > 2016 > 17 > 1 > 1-9
Human Mutation > 36 > 4 > 443 - 453
Orphanet Journal of Rare Diseases > 2015 > 10 > 1 > 1-8
European Journal of Nuclear Medicine and Molecular Imaging > 2015 > 42 > 10 > 1512-1521
Human Mutation > 34 > 8 > 1080 - 1084
Annals of Human Genetics > 77 > 4 > 336 - 343
Neuromuscular Disorders > 2012 > 22 > 1 > 66-72
Acta Neuropathologica > 2012 > 124 > 2 > 273-283
Annals of Neurology > 70 > 4 > 627 - 633
Neuromuscular Disorders > 2011 > 21 > 8 > 543-550
neurogenetics > 2010 > 11 > 1 > 13-19
The Lancet Neurology > 2009 > 8 > 12 > 1103-1110
NeuroMolecular Medicine > 2006 > 8 > 1-2 > 87-106