引用次数
引用: 22,169
H-指数: 74
I10-指数 : 184
出版物: 570
Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy
Marina Raffaele di Barletta , Enzo Ricci , Giuliana Galluzzi , Pietro Tonali
American Journal of Human Genetics 66 ( 4) 1407 -1412
353
2000
Heart involvement in lamin A/C related diseases.
Chikhaoui K , Demay L , Stora S , Bonne G
Archives Des Maladies Du Coeur Et Des Vaisseaux 99 ( 9) 848 -855
20
2006
Laminopathies affecting skeletal and cardiac muscles: clinical and pathophysiological aspects.
Ben Yaou R , Bonne G , Decostre
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 24 ( 2) 104
27
2005
Cardiac manifestations of laminopathies
Victor J , Dupuis Jm , Penisson-Besnier I , Bonne G
Archives Des Maladies Du Coeur Et Des Vaisseaux 97 ( 10) 973 -977
1
2004
Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy
Bonne G , Eymard B , François D , Marsac C
Revue Neurologique 147 462 -466
3
1991
[Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation].
Dubourg O , Forissier Je , Briault S , Schwartz K
Archives Des Maladies Du Coeur Et Des Vaisseaux 98 ( 1) 67 -70
1
2005
Pediatric laminopathies: Whole-body magnetic resonance imaging fingerprint and comparison with Sepn1 myopathy.
David Gómez-Andrés , Ivana Dabaj , Dominique Mompoint , Karolina Hankiewicz
Muscle & Nerve 54 ( 2) 192 -202
20
2016
INVITED REVIEW 177 A Narrative Review of Exercise-Associated Muscle Cramps: Factors that Contribute to Neuromuscular Fatigue and Management Implications Nicole L. Nelson, MSH, LMT and James R. Churilla, PhD, MPH ISSUES & OPINIONS 186 Clinical Follow-Up for Duchenne Muscular Dystrophy Newborn Screening: A Proposal
Jennifer M Kwon , Hoda Z Abdel-Hamid , Samiah A Al-Zaidy , Natalie Street
2016
Clinical relevance of atrial fibrillation/flutter, stroke, pacemaker implant, and heart failure in Emery-Dreifuss muscular dystrophy: a long-term longitudinal study.
Giuseppe Boriani , Margherita Gallina , Luciano Merlini , Gisèle Bonne
Stroke 34 ( 4) 901 -908
124
2003
Targeting the histone demethylase LSD1 prevents cardiomyopathy in a mouse model of laminopathy
Anne-Claire Guénantin , Imen Jebeniani , Julia Leschik , Erwan Watrin
Journal of Clinical Investigation 131 ( 1)
1
2021
Familial Hypertrophic Cardiomyopathy: From Mutations to Functional Defects
Gisèle Bonne , Lucie Carrier , Pascale Richard , Bernard Hainque
Circulation Research 83 ( 6) 580 -593
389
1998
Lamin A/C–mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy
Alexandre Méjat , Valérie Decostre , Juan Li , Laure Renou
Journal of Cell Biology 184 ( 1) 31 -44
96
2009
Systemic Glutathione Deficiency in LMNA-mutated: Relation With Left Ventricular Dysfunction and Functional Status
Christophe Meune , Lara Khouzami , Philippe Caramelle , Valérie Decostre
Circulation 120 ( suppl_18) S727 -S727
2009
Codon 102 of the Cardiac Troponin T Gene Is a Putative Hot Spot for Mutations in Familial Hypertrophic Cardiomyopathy
Jean-Franc¸ois Forissier , Lucie Carrier , Hend Farza , Gise`le Bonne
Circulation 94 ( 12) 3069 -3073
105
1996
MicroRNA expression profiling in patients with lamin A/C-associated muscular dystrophy
Nicolas Sylvius , Gise'le Bonne , Kees Straatman , Thimma Reddy
The FASEB Journal 25 ( 11) 3966 -3978
35
2011
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy.
Jeanne Flavigny , Pascale Richard , Richard Isnard , Lucie Carrier
Journal of Molecular Medicine 76 ( 3) 208 -214
119
1998
High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutation.
HENRI‐MARC BÉCANE , Gisele Bonne , Shaida Varnous , Antoine Muchir
Pacing and Clinical Electrophysiology 23 ( 11) 1661 -1666
207
2000
ELIZABETH N ANIONWU
GISELE BONNE , KETTY SCHWARTZ
echocardiography 53 1087 -94
1984
Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy
Howard J. Worman , Gisèle Bonne , Cecilia Östlund , Ketty Schwartz
Journal of Cell Science 114 ( 24) 4435 -4445
178
2001
[Towards an harmonization of diagnosis by NGS of neuromuscular diseases - Actions of the Molecular Genetics sub-group of FILNEMUS].
Aurelien Perrin , Philippe Latour , Vincent Procaccio , Claude Jardel
M S-medecine Sciences 20 -22
2018