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Results:
1-16
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Results: 16
Authors:
Dubourg, O
Tardieu, S
Birouk, N
Gouider, R
Leger, JM
Maisonobe, T
Brice, A
Bouche, P
LeGuern, E
Citation: O. Dubourg et al., The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocity, NEUROMUSC D, 11(5), 2001, pp. 458-463
Authors:
Le Forestier, N
Maisonobe, T
Spelle, L
Lesort, A
Salachas, F
Lacomblez, L
Samson, Y
Bouche, P
Meininger, V
Citation: N. Le Forestier et al., Primary lateral sclerosis: further clarification, J NEUR SCI, 185(2), 2001, pp. 95-100
Authors:
Dubourg, O
Tardieu, S
Birouk, N
Gouider, R
Leger, JM
Maisonobe, T
Brice, A
Bouche, P
LeGuern, E
Citation: O. Dubourg et al., Clinical, electrophysiological and molecular genetic characteristics of 93patients with X-linked Charcot-Marie-Tooth disease, BRAIN, 124, 2001, pp. 1958-1967
Authors:
Leger, JM
Chassande, B
Musset, L
Meininger, V
Bouche, P
Baumann, N
Citation: Jm. Leger et al., Intravenous immunoglobulin therapy in multifocal motor neuropathy - A double-blind, placebo-controlled study, BRAIN, 124, 2001, pp. 145-153
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:
Dejace, P
Gauthier, L
Bouche, P
Citation: P. Dejace et al., Populations of large mammals and ostriches in Zakouma National Park, Chad:their status and trends, REV ECOL, 55(4), 2000, pp. 305-320
Authors:
Dubourg, O
Barhoumi, C
Azzedine, H
Birouk, N
Brice, A
Bouche, P
Leguern, E
Citation: O. Dubourg et al., Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weakness, MUSCLE NERV, 23(10), 2000, pp. 1508-1514
Authors:
Le Forestier, N
Bouche, P
Citation: N. Le Forestier et P. Bouche, Motor conduction block, REV NEUROL, 156(6-7), 2000, pp. 678-679
Authors:
Le Forestier, N
Maisonobe, T
Spelle, L
Lesort, A
Salachas, F
Chassande, B
Bouche, P
Samson, Y
Meininger, V
Citation: N. Le Forestier et al., What's new in primary lateral sclerosis?, REV NEUROL, 156(4), 2000, pp. 364-371
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:
Tankere, F
Maisonobe, T
Naccache, L
Lamas, G
Soudant, J
Danziger, N
Bouche, P
Fournier, E
Willer, JC
Citation: F. Tankere et al., Further evidence for a central reorganisation of synaptic connectivity in patients with hypoglossal-facial anastomosis in man, BRAIN RES, 864(1), 2000, pp. 87-94
Authors:
Bouche, P
Le Forestier, N
Maisonobe, T
Fournier, E
Willer, JC
Citation: P. Bouche et al., Electrophysiological diagnosis of motor neuron disease and pure motor neuropathy, J NEUROL, 246(7), 1999, pp. 520-525
Authors:
Kubis, N
Durr, A
Gugenheim, M
Chneiweiss, H
Mazzetti, P
Brice, A
Bouche, P
Citation: N. Kubis et al., Polyneuropathy in autosomal dominant cerebellar ataxias: Phenotype-genotype correlation, MUSCLE NERV, 22(6), 1999, pp. 712-717
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
Authors:
Birouk, N
LeGuern, E
Bouche, P
Citation: N. Birouk et al., Is CMTX an axonopathy? Reply from the authors, NEUROLOGY, 52(2), 1999, pp. 433-433
Risultati:
1-16
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