Nicolas Chrestian

Dupré N, Chrestian N, Thiffault I, Brais B, Rouleau GA, Bouchard JP

[Hereditary ataxias, spastic parapareses and neuropathies in Eastern Canada]

Rev Neurol (Paris), 164 (1), 2008.

Résumé | Liens:

Chrestian N, Valdmanis PN, Echahidi N, Brunet D, Bouchard JP, Gould P, Rouleau GA, Champagne J, Dupré N

A novel mutation in a large French-Canadian family with LGMD1B

Can J Neurol Sci, 35 (3), 2008.

Résumé | Liens:

Rossignol E, Mathieu J, Thiffault I, Tetreault M, Dicaire MJ, Chrestian N, Dupre N, Puymirat J, Brais B

A novel founder SCN4A mutation causes painful cold-induced myotonia in French-Canadians

Neurology, 69 (20), 2007.

Résumé | Liens:

Dupre N, Gros-Louis F, Chrestian N, Verreault S, Brunet D, de Verteuil D, Brais B, Bouchard JP, Rouleau GA

Clinical and genetic study of autosomal recessive cerebellar ataxia type 1

Ann Neurol, 62 (1), 2007.

Résumé | Liens:

Chrestian N, Puymirat J, Bouchard JP, Dupré N

Myotonia congenita--a cause of muscle weakness and stiffness

Nat Clin Pract Neurol, 2 (7), 2006.

Résumé | Liens: