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Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies
Wahbi K, Ben Yaou R, Gandjbakhch E, et al.
Circulation, 2019
High Risk of Fatal and Nonfatal Venous Thromboembolism in Myotonic Dystrophy
Sochala M, Porcher R, Stojkovic T, et al.
Circulation, 2018, 138, 11, p 1169
Development and Validation of a New Scoring System to Predict Survival in Patients With Myotonic Dystrophy Type 1
Wahbi K, Porcher R, Laforêt P, et al.
JAMA Neurology, 2018, 75, 5, p 573
Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart Registry
Chong-Nguyen C, Wahbi K, Algalarrondo V, et al.
Circulation. Cardiovascular genetics, 2017, 10, 3
Incidence and predictors of sudden death, major conduction defects and sustained ventricular tachyarrhythmias in 1388 patients with myotonic dystrophy type 1
Wahbi K, Babuty D, Probst V, et al.
European heart journal, 2017, 38, 10, p 751
Prediction of long-term prognosis by heteroplasmy levels of the m.3243A>G mutation in patients with the mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome
Fayssoil A, Laforêt P, Bougouin W, et al.
European journal of neurology, 2017, 24, 2, p 255
Risk for Complications after Pacemaker or Cardioverter Defibrillator Implantations in Patients with Myotonic Dystrophy Type 1
Sochala M, Wahbi K, Sorbets E, et al.
Journal of Neuromuscular Diseases, 2017, 4, 3, p 175
Non Random Distribution of DMD Deletion Breakpoints and Implication of Double Strand Breaks Repair and Replication Error Repair Mechanisms
Marey I, Ben Yaou R, Deburgrave N, et al.
Journal of Neuromuscular Diseases, 2016, 3, 2, p 227
Atrial flutter in myotonic dystrophy type 1: Patient characteristics and clinical outcome
Wahbi K, Sebag FA, Lellouche N, et al.
Neuromuscular disorders : NMD, 2016, 26, 3, p 227
Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC
Avila Smirnow D, Gueneau L, Batonnet-Pichon S, et al.
Revue neurologique, 2016, 172, 10, p 594
Myofibrillar myopathies: State of the art, present and future challenges
Behin A, Salort-Campana E, Wahbi K, et al.
Revue neurologique, 2015, 171, 10, p 715
Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1
Wahbi K, Algalarrondo V, Bécane HM, et al.
Archives of Cardiovascular Diseases, 2013, 106, 12, p 635
Dilated cardiomyopathy in patients with mutations in Anoctamin 5
Wahbi K, Behin A, Bécane HM, et al.
International journal of cardiology, 2013, 168, 1, p 76
High risk of severe cardiac adverse events in patients with mitochondrial m.3243A>G mutation
Malfatti E, Laforêt P, Jardel C, et al.
Neurology, 2013, 80, 1, p 100
Electrophysiological study with prophylactic pacing and survival in adults with myotonic dystrophy and conduction system disease
Wahbi K, Meune C, Porcher R, et al.
JAMA. Journal of the American Medical Association, 2012, 307, 12, p 1292
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study
Wahbi K, Behin A, Charron P, et al.
Neuromuscular disorders : NMD, 2012, 22, 3, p 211
Improved survival by cardiac electrophysiologic study-based management of myotonic dystrophy type 1 associated with overt disease of the conduction system. A propensity analysis
Wahbi K, Meune C, Porcher R, et al.
Congrès : IXèmes Journées Annuelles de la Société française de Myologie (SFM) (3-5 novembre 2011; Angers)
2011, p. 14
Impaired myocardial deformation detected by speckle-tracking echocardiography in patients with myotonic dystrophy type 1
Wahbi K, Ederhy S, Bécane HM, et al.
International journal of cardiology, 2011, 152, 3, p 375
Preventive permanent pacing based on electrophysiological testing is associated with a reduction of global mortality in patients with myotonic dystrophy type 1
Wahbi K, Meune C, Bécane HM, et al.
Congrès : 4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France))
2011, p. 153
A high prevalence of Brugada syndrome among patients with Steinert's disease : a new insight into the pathophysiology of the Brugada syndrome (Abstract)
Wahbi K, Fressart V, Bécane HM, et al.
Journal of the American College of Cardiology, 2009, 53, 10, suppl A, p. A178
Left ventricular dysfunction and cardiac arrhythmias are frequent in type 2 myotonic dystrophy : a case control study
Wahbi K, Meune C, Bécane HM, et al.
Neuromuscular disorders : NMD, 2009, 19, 7, p. 468-472
Clinical heterogeneity of Duchenne muscular dystrophy (DMD) : definition of sub-phenotypes and predictive criteria by long-term follow-up
Desguerre I, Mayer M, Zeller R, et al.
PLoS ONE, 2009, 4, 2, e 1-10, 4347-p.
Clinical and imaging characteristics of myofibrillar myopathies : the Salpêtrière experience
Behin A, Stojkovic T, Claeys K, et al.
Congrès : Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France)
2008, p. 303
Clinical trials in cardiomyopathies linked to NMD : perindopril treatment in DMD and prevention od sudden death in laminopathies
Duboc D, Wahbi K, Meune C, et al.
Congrès : Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France)
2008, p. 20
Left ventricular non-compaction in a patient with myotonic dystrophy type 2
Wahbi K, Meune C, Bassez G, et al.
Neuromuscular disorders : NMD, 2008, 18, 4, p. 331-333
