AAAAAA

   
Results: 1-5 |
Results: 5

Authors: Gasser, T Dichgans, M Finsterer, J Hausmanowa-Petrusewicz, I Jurkat-Rott, K Klopstock, T Leguern, E Lehesjoki, AE Lehmann-Horn, F Lynch, T Morris, H Rossor, M Steinlein, OK Wood, N Zaremba, J Zeviani, M Zoharn, A
Citation: T. Gasser et al., EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - Second of two parts, EUR J NEUR, 8(5), 2001, pp. 407-424

Authors: Bernard, R Labelle, V Negre, P Tardieu, S Azulay, JP Malzac, P Mattei, JF Leguern, E Philip, N Levy, N
Citation: R. Bernard et al., Prenatal detection of a 17p11.2 duplication resulting from a rare recombination event and novel PCR-based strategy for molecular identification of Charcot-Marie-Tooth disease type 1A, EUR J HUM G, 8(3), 2000, pp. 229-235

Authors: Salih, MAM Maisonobe, T Kabiraj, M Al Rayess, M Al-Turaiki, MHS Akbar, M Tahan, A Urtizberea, JA Grid, D Hamadouche, T Guilbot, A Brice, A Leguern, E
Citation: Mam. Salih et al., Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity, NEUROMUSC D, 10(1), 2000, pp. 10-15

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: Allard, J Barron, S Trottier, S Cervera, P Daumas-Duport, C Leguern, E Brice, A Schwartz, JC Sokoloff, P
Citation: J. Allard et al., Edg-2 in myelin-forming cells: Isoforms, genomic mapping, and exclusion inCharcot-Marie-Tooth disease, GLIA, 26(2), 1999, pp. 176-185
Risultati: 1-5 |