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