Détail de l'auteur
Documents disponibles écrits par cet auteur (94)
trié(s) par (Pertinence décroissant(e), Date de parution décroissant(e), Date de parution décroissant(e), Système de projection du document croissant(e)) | Mettre toutes les notices dans le panier | Faire une suggestion | Ajouter un critère de recherche
Narrative review of glycogen storage disorder type III with a focus on neuromuscular, cardiac and therapeutic aspects
Berling É, Laforêt P, Wahbi K, et al.
Journal of inherited metabolic disease, 2020
Very low residual dystrophin quantity is associated with milder dystrophinopathy
de Feraudy Y, Yaou RB, Wahbi K, et al.
Annals of neurology, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathies
Guimaraes-Costa R, Fernandez-Eulate G, Wahbi K, et al.
European journal of neurology, 2020
The French national protocol for Kennedy's disease (SBMA): consensus diagnostic and management recommendations
Pradat PF, Bernard E, Corcia P, et al.
Orphanet journal of rare diseases, 2020, 15, 1, p 90
Cardiovascular complications of lipodystrophic syndromes - focus on laminopathies
Mosbah H, Vatier C, Boccara F, et al.
Annales d'endocrinologie, 2020
Guidance for the care of neuromuscular patients during the COVID-19 pandemic outbreak from the French Rare Health Care for Neuromuscular Diseases Network
Solé G, Salort-Campana E, Pereon Y, et al.
Revue neurologique, 2020, 176, 6, p 507
Response by Wahbi and Stalens to Letter Regarding Article, "Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies"
Wahbi K, Stalens C
Circulation, 2019, 140, 23
A high prevalence of arterial hypertension in patients with mitochondrial diseases
Chong-Nguyen C, Stalens C, Goursot Y, et al.
Journal of inherited metabolic disease, 2019
X-linked Emery-Dreifuss muscular dystrophy manifesting with adult onset axial weakness, camptocormia, and minimal joint contractures
Brisset M, Ben Yaou R, Carlier RY, et al.
Neuromuscular disorders : NMD, 2019, 29, 9, p 678
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
Congenital myopathies are mainly associated with a mild cardiac phenotype
Petri H, Wahbi K, Witting N, et al.
Journal of neurology, 2019, 266, 6, p 1367
Cardiovascular manifestations of myotonic dystrophy.
Wahbi K, Furling D
Trends in cardiovascular medicine, 2019
Comprehensive evaluation of structural and functional myocardial impairments in Becker muscular dystrophy using quantitative cardiac magnetic resonance imaging
Marty B, Gilles R, Toussaint M, et al.
European heart journal cardiovascular Imaging, 2018
Mitochondrial disease: learning from Charlie's lesson, trying to cure, trying much more to care
Limongelli G, Limongelli G, Wahbi K
Future Cardiology, 2018
Genotype and other determinants of respiratory function in myotonic dystrophy type 1
Boussaïd G, Wahbi K, Laforêt P, et al.
Neuromuscular disorders : NMD, 2018, 28, 3, p 222
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
Lamin and the heart
Captur G, Arbustini E, Bonne G, et al.
Heart (British Cardiac Society), 2018, 104, 6, p 468
Rescue of biosynthesis of nicotinamide adenine dinucleotide protects the heart in cardiomyopathy caused by lamin A/C gene mutation
Vignier N, Vignier N, Chatzifrangkeskou M, et al.
Human molecular genetics, 2018, 27, 22, p 3870
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
Two new cases of mitochondrial myopathy with exercise intolerance, hyperlactatemia and cardiomyopathy, caused by recessive SLC25A4 mutations
Tosserams A, Papadopoulos C, Jardel C, et al.
Mitochondrion, 2018, 39, p 26
Non invasive mechanical ventilation in DM1: The strong correlation between lung function, neurological-cognitive function and CTG repeats
Lofaso F, Prigent H, Annane D, et al.
Neuromuscular disorders : NMD, 2018, 28, 10, p 894
Left bundle branch block in Duchenne muscular dystrophy: Prevalence, genetic relationship and prognosis
Fayssoil A, Ben Yaou R, Ogna A, et al.
PLoS ONE, 2018, 13, 1
Cardiac manifestations of congenital LMNA-related muscular dystrophy in children: three case reports and recommendations for care
Heller F, Dabaj I, Mah JK, et al.
Cardiology in the young, 2017, 27, 6, p 1076
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
Clinical profiles and prognosis of acute heart failure in adult patients with dystrophinopathies on home mechanical ventilation
Fayssoil A, Yaou RB, Ogna A, et al.
ESC heart failure, 2017, 4, 4, p 527
