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Results: 1-6 |
Results: 6

Authors: Hand, CK Khoris, J Salachas, F Gros-Louis, F Lopes, AAS Mayeux-Portas, V Brown, RH Meininger, V Camu, W Rouleau, GA
Citation: Ck. Hand et al., A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q, AM J HU GEN, 70(1), 2002, pp. 251-256

Authors: Hand, CK Mayeux-Portas, V Khoris, J Briolotti, V Clavelou, P Camu, W Rouleau, GA
Citation: Ck. Hand et al., Compound heterozygosity and variable penetrance in SOD1 amyotrophic lateral sclerosis pedigrees - Reply, ANN NEUROL, 50(4), 2001, pp. 554-554

Authors: Hand, CK Mayeux-Portas, V Khoris, J Briolotti, V Clavelou, P Camu, W Rouleau, GA
Citation: Ck. Hand et al., Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family, ANN NEUROL, 49(2), 2001, pp. 267-271

Authors: Khoris, J Moulard, B Briolotti, V Hayer, M Durieux, A Clavelou, P Malafosse, A Rouleau, GA Camu, W
Citation: J. Khoris et al., Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country, EUR J NEUR, 7(2), 2000, pp. 207-211

Authors: Camu, W Khoris, J Moulard, B Salachas, F Briolotti, V Rouleau, GA Meininger, V
Citation: W. Camu et al., Genetics of familial ALS and consequences for diagnosis, J NEUR SCI, 165, 1999, pp. S21-S26

Authors: Khoris, J Pages, M
Citation: J. Khoris et M. Pages, Opsoclonus-myoclonus in adults: 4 cases., ANN MED IN, 150(4), 1999, pp. 283-286
Risultati: 1-6 |