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Results: 1-13 |
Results: 13
Myoblast transplantation for heart failure
Authors: Menasche, P Hagege, AA Scorsin, M Pouzet, B Desnos, M Duboc, D Schwartz, K Vilquin, JT Marolleau, JP
Citation: P. Menasche et al., Myoblast transplantation for heart failure, LANCET, 357(9252), 2001, pp. 279-280
Proximal myotonial myopathy (PROMM): clinical and histology study.
Authors: Bassez, G Attarian, S Laforet, P Azulay, JP Rouche, A Ferrer, X Urtizberea, JA Pellissier, JF Duboc, D Fardeau, M Pouget, J Eymard, B
Citation: G. Bassez et al., Proximal myotonial myopathy (PROMM): clinical and histology study., REV NEUROL, 157(2), 2001, pp. 209-218
Comparison of single-shot east spin-echo and conventional spin-echo sequences for MR imaging of the heart: Initial experience
Authors: Vignaux, OB Augui, J Coste, J Argaud, C Le Roux, P Carlier, PG Duboc, D Legmann, P
Citation: Ob. Vignaux et al., Comparison of single-shot east spin-echo and conventional spin-echo sequences for MR imaging of the heart: Initial experience, RADIOLOGY, 219(2), 2001, pp. 545-550
Is skeletal myoblast transplantation clinically relevant in the era of angiotensin-converting enzyme inhibitors?
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
Autologous skeletal myoblast transplantation for cardiac failure. First clinical case report.
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
Brain natiuretic peptide and cardiac failure.
Authors: Jourdain, P Funck, F Fulla, Y Bellorini, M Guillard, N Loiret, J Thebault, B Duboc, D Desnos, M
Citation: P. Jourdain et al., Brain natiuretic peptide and cardiac failure., ARCH MAL C, 94(2), 2001, pp. 124-129
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene
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
High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutation
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
Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alpha beta-cristallin gene
Authors: Fardeau, M Vicart, P Caron, A Chateau, D Chevallay, M Collin, H Chapon, F Duboc, D Eymard, B Tome, FMS Dupret, JM Paulin, D Guicheney, P
Citation: M. Fardeau et al., Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alpha beta-cristallin gene, REV NEUROL, 156(5), 2000, pp. 497-504
Sudden death in myotonic dystrophy: The potential role of bundle-branch reentry - Response
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
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
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
Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy
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
Pericardial and myocardial adiastole in rheumatoid arthritis.
Authors: Erciyes, D Mousseaux, E Cabanes, L Dougados, M Mallet, V Erlinger, S Gandjbakhch, I Duboc, D Fouchard, J
Citation: D. Erciyes et al., Pericardial and myocardial adiastole in rheumatoid arthritis., ARCH MAL C, 92(10), 1999, pp. 1381-1384
Risultati: 1-13 |