P. Mouton

发表

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

J. Weissenbach, H. Chabriat, E. Cabanis, 1996, Nature.

Notch3 Mutations in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL), a Mendelian Condition Causing Stroke and Vascular Dementia

J. Weissenbach, H. Chabriat, E. Cabanis, 1997, Annals of the New York Academy of Sciences.

Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion

A. Brice, N. Birouk, R. Gouider, 1999, Neurology.

Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsies

A. Brice, P. Bouche, O. Dubourg, 2000, Neuromuscular Disorders.

[Hereditary neuropathy with liability to pressure palsies].

R. Gouider, E. Le Guern, T. Maisonobe, 2000, Revue neurologique.

[True neurological thoracic outlet syndrome].

J. Willer, T. Maisonobe, N. le Forestier, 2000, Revue neurologique.

Macrophagic myofasciitis associated with inclusion body myositis: a report of three cases

J. Viallard, F. Authier, P. Mouton, 2001, Neuromuscular Disorders.

Comparison of spinal magnetic resonance imaging and classical clinical factors in predicting motor capacity in amyotrophic lateral sclerosis

Jeanne M. Miller, K. Dujardin, V. Marchand-Pauvert, 2023, Journal of Neurology.

Case report Macrophagic myofasciitis associated with inclusion body myositis: a report of three cases

P. Mouton, P. Cherin, S. Herson, 2001 .