V. Briolotti

发表

Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country

A. Malafosse, G. Rouleau, G. Rouleau, 2000, European journal of neurology.

N19S, a new SOD1 mutation in sporadic amyotrophic lateral sclerosis: No evidence for disease causation

P. Corcia, W. Camu, G. Besson, 2003, Annals of neurology.

G. Rouleau, W. Camu, P. Clavelou, 2001 .

Association between centromeric deletions of the SMN gene and sporadic adult‐onset lower motor neuron disease

A. Malafosse, V. Meininger, F. Salachas, 1998, Annals of neurology.

Genetics of familial ALS and consequences for diagnosis 1

V. Meininger, F. Salachas, G. Rouleau, 1999, Journal of the Neurological Sciences.

Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family

G. Rouleau, W. Camu, P. Clavelou, 2001, Annals of neurology.