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Auteur Wahbi K |
Documents disponibles écrits par cet auteur (94)



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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
Revue : Journal of inherited metabolic disease Titre : Narrative review of glycogen storage disorder type III with a focus on neuromuscular, cardiac and therapeutic aspects Type de document : Article Auteurs : Berling É ; Laforêt P ; Wahbi K ; Labrune P ; Petit F ; Ronzitti G ; O'Brien A Editeur : United States Année de publication : 24/12/2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 33368379 / DOI : 10.1002/jimd.12355
N° Profil MNM : 2020123 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/33368379 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Very low residual dystrophin quantity is associated with milder dystrophinopathy
de Feraudy Y, Yaou RB, Wahbi K, et al.
Annals of neurology, 2020
Revue : Annals of neurology Titre : Very low residual dystrophin quantity is associated with milder dystrophinopathy Type de document : Article Auteurs : de Feraudy Y ; Yaou RB ; Wahbi K ; Stalens C ; Stantzou A ; Laugel V ; Desguerre I ; Servais L ; Leturcq F ; Amthor H Editeur : United States Année de publication : 07/11/2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 33159473 / DOI : 10.1002/ana.25951
N° Profil MNM : 2020111 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/33159473 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
Revue : European journal of neurology Titre : Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathies Type de document : Article Auteurs : Guimaraes-Costa R ; Fernandez-Eulate G ; Wahbi K ; Leturcq F ; Malfatti E ; Behin A ; Leonard-Louis S ; Desguerre I ; Barnerias C ; Nougues MC ; Isapof A ; Estournet-Mathiaud B ; Quijano-Roy S ; Fayssoil A ; Orlikowski D ; Fauroux B ; Richard I ; Semplicini C ; Romero NB ; Querin G ; Eymard B ; Laforêt P ; Stojkovic T Editeur : England Année de publication : 14/10/2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 33051934 / DOI : 10.1111/ene.14592
N° Profil MNM : 2020102 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/33051934 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
Revue : Orphanet journal of rare diseases, 15, 1 Titre : The French national protocol for Kennedy's disease (SBMA): consensus diagnostic and management recommendations Type de document : Article Auteurs : Pradat PF, Auteur ; Bernard E ; Corcia P ; Couratier P ; Jublanc C ; Querin G ; Morélot Panzini C ; Salachas F ; Vial C ; Wahbi K ; Bede P ; Desnuelle C Année de publication : 04/2020 Pages : p 90 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32276665 / DOI : 10.1186/s13023-020-01366-z
N° Profil MNM : 2020041 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32276665 Voir aussiAvis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Cardiovascular complications of lipodystrophic syndromes - focus on laminopathies
Mosbah H, Vatier C, Boccara F, et al.
Annales d'endocrinologie, 2020
Revue : Annales d'endocrinologie Titre : Cardiovascular complications of lipodystrophic syndromes - focus on laminopathies Type de document : Article Auteurs : Mosbah H, Auteur ; Vatier C ; Boccara F ; Jéru I ; Vantyghem MC ; Donadille B ; Wahbi K ; Vigouroux C Editeur : France Année de publication : 03/2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32201029 / DOI : 10.1016/j.ando.2020.03.002
N° Profil MNM : 2020032 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32201029 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
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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
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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
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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
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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
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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
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Cardiovascular manifestations of myotonic dystrophy.
Wahbi K, Furling D
Trends in cardiovascular medicine, 2019
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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
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Mitochondrial disease: learning from Charlie's lesson, trying to cure, trying much more to care
Limongelli G, Limongelli G, Wahbi K
Future Cardiology, 2018
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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
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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
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Lamin and the heart
Captur G, Arbustini E, Bonne G, et al.
Heart (British Cardiac Society), 2018, 104, 6, p 468
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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
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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
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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
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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
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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
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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
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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
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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
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