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Results:
1-7
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Results: 7
Authors:
Cherin, P
Menard, D
Mouton, P
Viallard, JF
Le Hello, C
Authier, FJ
Gherardi, RK
Coquet, M
Herson, S
Leroi, JP
Citation: P. Cherin et al., Macrophagic myofasciitis associated with inclusion body myositis: a reportof three cases, NEUROMUSC D, 11(5), 2001, pp. 452-457
Authors:
Dubourg, O
Mouton, P
Brice, A
LeGuern, E
Bouche, P
Citation: O. Dubourg et al., Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsies, NEUROMUSC D, 10(3), 2000, pp. 206-208
Authors:
Mouton, P
Defer, GL
Citation: P. Mouton et Gl. Defer, Behavioral disorders due to acute vigabatrin intoxication, REV NEUROL, 156(2), 2000, pp. 184-186
Authors:
Bouche, P
Mouton, P
Gouider, R
Dubourg, O
Le Guern, E
Maisonobe, T
le Forestier, N
Citation: P. Bouche et al., Hereditary neuropathy by pressure hypersensitivity, REV NEUROL, 156(10), 2000, pp. 915-919
Authors:
Le Forestier, N
Mouton, P
Maisonobe, T
Fournier, E
Moulonguet, A
Willer, JC
Bouche, P
Citation: N. Le Forestier et al., True neurological thoracic outlet syndrome: 10 cases, REV NEUROL, 156(1), 2000, pp. 34-40
Authors:
Mouton, P
Maisonobe, T
Behin, A
Cohen, L
Pierrot-Deseilligny, C
Citation: P. Mouton et al., Distal Miyoshi muscular dystrophy on a Moroccan patient, PRESSE MED, 28(9), 1999, pp. 476-478
Authors:
Mouton, P
Tardieu, S
Gouider, R
Birouk, N
Maisonabe, T
Dubourg, O
Brice, A
LeGuern, E
Bouche, P
Citation: P. Mouton et al., Spectrum of clinical and electrophysiologic features in HNPP patients withthe 17p11.2 deletion, NEUROLOGY, 52(7), 1999, pp. 1440-1446
Risultati:
1-7
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