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Results:
1-8
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Results: 8
Authors:
Brassat, D
Citation: D. Brassat, Indications for etiological treatment (excepting primary progressive MS), REV NEUROL, 157(8-9), 2001, pp. 1014-1028
Authors:
Durr, A
Brassat, D
Brice, A
Citation: A. Durr et al., The DYT1 mutation and nonfamilial primary torsion dystonia - In reply, ARCH NEUROL, 58(4), 2001, pp. 682-682
Authors:
Clanet, MG
Brassat, D
Citation: Mg. Clanet et D. Brassat, The management of multiple sclerosis patients, CURR OP NEU, 13(3), 2000, pp. 263-270
Authors:
Werring, DJ
Brassat, D
Droogan, AG
Clark, CA
Symms, MR
Barker, GJ
MacManus, DG
Thompson, AJ
Miller, DH
Citation: Dj. Werring et al., The pathogenesis of lesions and normal-appearing white matter changes in multiple sclerosis - A serial diffusion MRI study, BRAIN, 123, 2000, pp. 1667-1676
Authors:
Brassat, D
Camuzat, A
Vidailhet, M
Feki, I
Jedynak, P
Klap, P
Agid, Y
Durr, A
Brice, A
Citation: D. Brassat et al., Frequency of the DYT1 mutation in primary torsion dystonia without family history, ARCH NEUROL, 57(3), 2000, pp. 333-335
Authors:
Herman-Bert, A
Stevanin, G
Netter, JC
Rascol, O
Brassat, D
Calvas, P
Camuzat, A
Yuan, QP
Schalling, M
Durr, A
Brice, A
Citation: A. Herman-bert et al., Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation, AM J HU GEN, 67(1), 2000, pp. 229-235
Authors:
Brassat, D
Durr, A
Agid, Y
Brice, A
Citation: D. Brassat et al., Genetic aspect of Parkinson's disease., REV MED IN, 20(8), 1999, pp. 709-714
Authors:
Brassat, D
Azais-Vuillemin, C
Yaouanq, J
Semana, G
Reboul, J
Cournu, I
Mertens, C
Edan, G
Lyon-Caen, O
Clanet, C
Fontaine, B
Citation: D. Brassat et al., Familial factors influence disability in MS multiplex families, NEUROLOGY, 52(8), 1999, pp. 1632-1636
Risultati:
1-8
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