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Rabah Ben Yaou

Showing results (1-10 of 54) with videos related to

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Biochemical Society Transactions|November 23, 2011
Clinical and genetic heterogeneity in laminopathiesAnne T Bertrand, Khadija Chikhaoui, Rabah Ben Yaou, et al.
Biologie Aujourd'Hui|October 11, 2011
[Laminopathies: one gene, several diseases]Anne T Bertrand, Khadija Chikhaoui, Rabah Ben Yaou, et al.
Journal of Clinical Medicine|November 13, 2021
Preclinical Advances of Therapies for LaminopathiesLouise Benarroch, Enzo Cohen, Antonio Atalaia, et al.
Journal of Neuromuscular Diseases|March 8, 2021
Laminopathies' Treatments Systematic Review: A Contribution Towards a 'Treatabolome'Antonio Atalaia, Rabah Ben Yaou, Karim Wahbi, et al.
Novartis Foundation Symposium|March 19, 2005
Genetics of laminopathiesRabah Ben Yaou, Antoine Muchir, Takuro Arimura, et al.
Muscle & Nerve|September 17, 2011
Cardioembolic stroke prompting diagnosis of LMNA-associated Emery-Dreifuss muscular dystrophyLuis Redondo-Vergé, Rabah Ben Yaou, María Fernández-Recio, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 14, 2025
Duchenne muscular dystrophy: the French Dystrophinopathies Registry (DYS Registry)Isabelle Desguerre, Romain Glandier, Julie Lejeune, et al.
Cells|April 5, 2020
Lamin A/C Assembly Defects in <i>LMNA</i>-Congenital Muscular Dystrophy Is Responsible for the Increased Severity of the Disease Compared with Emery-Dreifuss Muscular DystrophyAnne T Bertrand, Astrid Brull, Feriel Azibani, et al.
Orphanet Journal of Rare Diseases|July 11, 2012
Assessment of the structural and functional impact of in-frame mutations of the DMD gene, using the tools included in the eDystrophin online databaseAurélie Nicolas, Céline Lucchetti-Miganeh, Rabah Ben Yaou, et al.
Annals of Neurology|November 7, 2020
Very Low Residual Dystrophin Quantity Is Associated with Milder DystrophinopathyYvan de Feraudy, Rabah Ben Yaou, Karim Wahbi, et al.
Pageof 6

Showing results (1-10 of 54) with videos related to

Sort By:
Pageof 6
Biochemical Society Transactions|November 23, 2011
Clinical and genetic heterogeneity in laminopathiesAnne T Bertrand, Khadija Chikhaoui, Rabah Ben Yaou, et al.
Biologie Aujourd'Hui|October 11, 2011
[Laminopathies: one gene, several diseases]Anne T Bertrand, Khadija Chikhaoui, Rabah Ben Yaou, et al.
Journal of Clinical Medicine|November 13, 2021
Preclinical Advances of Therapies for LaminopathiesLouise Benarroch, Enzo Cohen, Antonio Atalaia, et al.
Journal of Neuromuscular Diseases|March 8, 2021
Laminopathies' Treatments Systematic Review: A Contribution Towards a 'Treatabolome'Antonio Atalaia, Rabah Ben Yaou, Karim Wahbi, et al.
Novartis Foundation Symposium|March 19, 2005
Genetics of laminopathiesRabah Ben Yaou, Antoine Muchir, Takuro Arimura, et al.
Muscle & Nerve|September 17, 2011
Cardioembolic stroke prompting diagnosis of LMNA-associated Emery-Dreifuss muscular dystrophyLuis Redondo-Vergé, Rabah Ben Yaou, María Fernández-Recio, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 14, 2025
Duchenne muscular dystrophy: the French Dystrophinopathies Registry (DYS Registry)Isabelle Desguerre, Romain Glandier, Julie Lejeune, et al.
Cells|April 5, 2020
Lamin A/C Assembly Defects in <i>LMNA</i>-Congenital Muscular Dystrophy Is Responsible for the Increased Severity of the Disease Compared with Emery-Dreifuss Muscular DystrophyAnne T Bertrand, Astrid Brull, Feriel Azibani, et al.
Orphanet Journal of Rare Diseases|July 11, 2012
Assessment of the structural and functional impact of in-frame mutations of the DMD gene, using the tools included in the eDystrophin online databaseAurélie Nicolas, Céline Lucchetti-Miganeh, Rabah Ben Yaou, et al.
Annals of Neurology|November 7, 2020
Very Low Residual Dystrophin Quantity Is Associated with Milder DystrophinopathyYvan de Feraudy, Rabah Ben Yaou, Karim Wahbi, et al.
Pageof 6