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[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations].
Ben Yaou R, Bécane HM, Demay L, Laforet P, Hannequin D, Bohu PA, Drouin-Garraud V, Ferrer X, Mussini JM, Ollagnon E, Petiot P, Penisson-Besnier I, Streichenberger N, Toutain A, Richard P, Eymard B, Bonne G. Ben Yaou R, et al. Rev Neurol (Paris). 2005 Jan;161(1):42-54. doi: 10.1016/s0035-3787(05)84972-0. Rev Neurol (Paris). 2005. PMID: 15678000 French.
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, Delort F, Bécane HM, Claeys K, Beuvin M, Goudeau B, Jais JP, Nelson I, Richard P, Ben Yaou R, Romero NB, Wahbi K, Mathis S, Voit T, Furst D, van der Ven P, Gil R, Vicart P, Fardeau M, Bonne G, Behin A. Avila-Smirnow D, et al. Among authors: ben yaou r. Rev Neurol (Paris). 2016 Oct;172(10):594-606. doi: 10.1016/j.neurol.2016.07.017. Epub 2016 Sep 12. Rev Neurol (Paris). 2016. PMID: 27633507 Review.
Heart involvement in lamin A/C related diseases.
Ben Yaou R, Gueneau L, Demay L, Stora S, Chikhaoui K, Richard P, Bonne G. Ben Yaou R, et al. Arch Mal Coeur Vaiss. 2006 Sep;99(9):848-55. Arch Mal Coeur Vaiss. 2006. PMID: 17067107 Review.
Cardiometabolic assessment of lamin A/C gene mutation carriers: a phenotype-genotype correlation.
Kwapich M, Lacroix D, Espiard S, Ninni S, Brigadeau F, Kouakam C, Degroote P, Laurent JM, Tiffreau V, Jannin A, Humbert L, Ben Hamou A, Tard C, Ben Yaou R, Lamblin N, Klug D, Richard P, Vigouroux C, Bonne G, Vantyghem MC; Diamenord–AEDNL Working Group. Kwapich M, et al. Among authors: ben hamou a, ben yaou r. Diabetes Metab. 2019 Sep;45(4):382-389. doi: 10.1016/j.diabet.2018.09.006. Epub 2018 Oct 1. Diabetes Metab. 2019. PMID: 30287275
54 results