Authors:
Hetet, G
Grandchamp, B
Bouchier, C
Nicaud, V
Tiret, L
Roizes, G
Desnos, M
Schwartz, K
Dorent, R
Komajda, M
Citation: G. Hetet et al., Idiopathic dilated cardiomyopathy: lack of association with haemochromatosis gene in the CARDIGENE study, HEART, 86(6), 2001, pp. 702-703
Authors:
Vilquin, JT
Kennel, PF
Paturneau-Jouas, M
Chapdelaine, P
Boissel, N
Delaere, P
Tremblay, JP
Scherman, D
Fiszman, MY
Schwartz, K
Citation: Jt. Vilquin et al., Electro transfer of naked DNA in the skeletal muscles of animal models of muscular dystrophies, GENE THER, 8(14), 2001, pp. 1097-1107
Authors:
Kitaguchi, T
Matsubara, S
Sato, M
Miyamoto, K
Hirai, S
Schwartz, K
Bonne, G
Citation: T. Kitaguchi et al., A missense mutation in the exon 8 of lamin A/C gene in a Japanese case of autosomal dominant limb-girdle muscular dystrophy and cardiac conduction block, NEUROMUSC D, 11(6-7), 2001, pp. 542-546
Authors:
Kotomin, EA
Kashcheyevs, V
Kuzovkov, VN
Schwartz, K
Trautmann, C
Citation: Ea. Kotomin et al., Modeling of primary defect aggregation in tracks of swift heavy ions in LiF - art. no. 144108, PHYS REV B, 6414(14), 2001, pp. 4108
Authors:
Pouzet, B
Ghostine, S
Vilquin, JT
Garcin, I
Scorsin, M
Hagege, AA
Duboc, D
Schwartz, K
Menasche, P
Citation: B. Pouzet et al., Is skeletal myoblast transplantation clinically relevant in the era of angiotensin-converting enzyme inhibitors?, CIRCULATION, 104(12), 2001, pp. I223-I228
Authors:
Schwartz, PJ
Priori, SG
Spazzolini, C
Moss, AJ
Vincent, GM
Napolitano, C
Denjoy, I
Guicheney, P
Breithardt, G
Keating, MT
Towbin, JA
Beggs, AH
Brink, P
Wilde, AAM
Toivonen, L
Zareba, W
Robinson, JL
Timothy, KW
Corfield, V
Wattanasirichaigoon, D
Corbett, C
Haverkamp, W
Schulze-Bahr, E
Lehmann, MH
Schwartz, K
Coumel, P
Bloise, R
Citation: Pj. Schwartz et al., Genotype-phenotype correlation in the long-QT syndrome - Gene-specific triggers for life-threatening arrhythmias, CIRCULATION, 103(1), 2001, pp. 89-95
Authors:
Menasche, P
Hagege, A
Scorsin, M
Pouzet, B
Desnos, M
Duboc, D
Schwartz, K
Vilquin, JT
Marolleau, JP
Citation: P. Menasche et al., Autologous skeletal myoblast transplantation for cardiac failure. First clinical case report., ARCH MAL C, 94(3), 2001, pp. 180-182
Authors:
Pouzet, B
Vilquin, JT
Hagege, AA
Scorsin, M
Messas, E
Fiszman, M
Schwartz, K
Menasche, P
Citation: B. Pouzet et al., Factors affecting functional outcome after autologous skeletal myoblast transplantation, ANN THORAC, 71(3), 2001, pp. 844-850
Authors:
Muchir, A
Bonne, G
van der Kool, AJ
van Meegen, M
Baas, F
Bolhuis, PA
de Visser, M
Schwartz, K
Citation: A. Muchir et al., Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B), HUM MOL GEN, 9(9), 2000, pp. 1453-1459
Authors:
Tardif-de Gery, S
Vilquin, JT
Carlier, P
Raynaud, JS
Wary, C
Schwartz, K
Leroy-Willig, A
Citation: S. Tardif-de Gery et al., Muscular transverse relaxation time measurement by magnetic resonance imaging at 4 Tesla in normal and dystrophic dy/dy and dy(2j)/dy(2j) mice, NEUROMUSC D, 10(7), 2000, pp. 507-513
Authors:
Ondo, W
Hunter, C
Vuong, KD
Schwartz, K
Jankovic, J
Citation: W. Ondo et al., Gabapentin for essential tremor: A multiple-dose, double-blind, placebo-controlled trial, MOVEMENT D, 15(4), 2000, pp. 678-682
Authors:
Tiret, L
Mallet, C
Poirier, O
Nicaud, V
Millaire, A
Bouhour, JB
Roizes, G
Desnos, M
Dorent, R
Schwartz, K
Cambien, F
Komajda, M
Citation: L. Tiret et al., Lack of association between polymorphisms of eight candidate genes and idiopathic dilated cardiomyopathy - The CARDIGENE study, J AM COL C, 35(1), 2000, pp. 29-35
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