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Results: 5

Authors: Bonne, G Mercuri, E Muchir, A Urtizberea, A Becane, HM Recan, D Merlini, L Wehnert, M Boor, R Reuner, U Vorgerd, M Wicklein, EM Eymard, B Duboc, D Penisson-Besnier, I Cuisset, JM Ferrer, X Desguerre, I Lacombe, D Bushby, K Pollitt, C Toniolo, D Fardeau, M Schwartz, K Muntoni, F
Citation: G. Bonne et al., Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene, ANN NEUROL, 48(2), 2000, pp. 170-180

Authors: Becane, HM Bonne, G Varnous, S Muchir, A Ortega, V Hammouda, E Urtizberea, JA Lavergne, T Fardeau, M Eymard, B Weber, S Schwartz, K Duboc, D
Citation: Hm. Becane et al., High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutation, PACE, 23(11), 2000, pp. 1661-1666

Authors: Lazarus, A Varin, J Ounnoughene, Z Radvanyi, H Junien, C Coste, J Laforet, P Eymard, B Becane, HM Weber, S Duboc, D
Citation: A. Lazarus et al., Sudden death in myotonic dystrophy: The potential role of bundle-branch reentry - Response, CIRCULATION, 101(5), 2000, pp. E73-E73

Authors: Bonne, G Di Barletta, MR Varnous, S Becane, HM Hammouda, EH Merlini, L Muntoni, F Greenberg, CR Gary, F Urtizberea, JA Duboc, D Fardeau, M Toniolo, D Schwartz, K
Citation: G. Bonne et al., Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy, NAT GENET, 21(3), 1999, pp. 285-288

Authors: Lazarus, A Varin, J Ounnoughene, Z Radvanyi, H Junien, C Coste, J Laforet, P Eymard, B Becane, HM Weber, S Duboc, D
Citation: A. Lazarus et al., Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy, CIRCULATION, 99(8), 1999, pp. 1041-1046
Risultati: 1-5 |