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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
2001 1
2004 1
2005 4
2006 3
2007 1
2008 1
2009 1
2010 2
2011 3
2012 1
2013 3
2014 3
2015 5
2016 3
2017 2
2018 3
2019 6
2020 2
2021 8
2022 2
2023 1
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49 results
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Page 1
Preclinical Advances of Therapies for Laminopathies.
Benarroch L, Cohen E, Atalaia A, Ben Yaou R, Bonne G, Bertrand AT. Benarroch L, et al. Among authors: ben yaou r. J Clin Med. 2021 Oct 21;10(21):4834. doi: 10.3390/jcm10214834. J Clin Med. 2021. PMID: 34768351 Free PMC article. Review.
Emery-Dreifuss Muscular Dystrophy.
Bonne G, Leturcq F, Ben Yaou R. Bonne G, et al. Among authors: ben yaou r. 2004 Sep 29 [updated 2019 Aug 15]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 2004 Sep 29 [updated 2019 Aug 15]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 20301609 Free Books & Documents. Review.
[MLIP: a novel gene causing rhabdomyolysis].
Ben Yaou R. Ben Yaou R. Med Sci (Paris). 2021 Nov;37 Hors série n° 1:48. doi: 10.1051/medsci/2021193. Epub 2021 Dec 8. Med Sci (Paris). 2021. PMID: 34878397 Free article. French. No abstract available.
Genetics of laminopathies.
Ben Yaou R, Muchir A, Arimura T, Massart C, Demay L, Richard P, Bonne G. Ben Yaou R, et al. Novartis Found Symp. 2005;264:81-90; discussion 90-97, 227-30. Novartis Found Symp. 2005. PMID: 15773749 Review.
[Laminopathies: one gene, several diseases].
Bertrand AT, Chikhaoui K, Ben Yaou R, Bonne G. Bertrand AT, et al. Among authors: ben yaou r. Biol Aujourdhui. 2011;205(3):147-62. doi: 10.1051/jbio/2011017. Epub 2011 Oct 11. Biol Aujourdhui. 2011. PMID: 21982404 Review. French.
Very Low Residual Dystrophin Quantity Is Associated with Milder Dystrophinopathy.
de Feraudy Y, Ben Yaou R, Wahbi K, Stalens C, Stantzou A, Laugel V, Desguerre I; FILNEMUS Network; Servais L, Leturcq F, Amthor H. de Feraudy Y, et al. Among authors: ben yaou r. Ann Neurol. 2021 Feb;89(2):280-292. doi: 10.1002/ana.25951. Epub 2020 Nov 24. Ann Neurol. 2021. PMID: 33159473 Free PMC article.
International retrospective natural history study of LMNA-related congenital muscular dystrophy.
Ben Yaou R, Yun P, Dabaj I, Norato G, Donkervoort S, Xiong H, Nascimento A, Maggi L, Sarkozy A, Monges S, Bertoli M, Komaki H, Mayer M, Mercuri E, Zanoteli E, Castiglioni C, Marini-Bettolo C, D'Amico A, Deconinck N, Desguerre I, Erazo-Torricelli R, Gurgel-Giannetti J, Ishiyama A, Kleinsteuber KS, Lagrue E, Laugel V, Mercier S, Messina S, Politano L, Ryan MM, Sabouraud P, Schara U, Siciliano G, Vercelli L, Voit T, Yoon G, Alvarez R, Muntoni F, Pierson TM, Gómez-Andrés D, Reghan Foley A, Quijano-Roy S, Bönnemann CG, Bonne G. Ben Yaou R, et al. Brain Commun. 2021 Apr 11;3(3):fcab075. doi: 10.1093/braincomms/fcab075. eCollection 2021 Jul. Brain Commun. 2021. PMID: 34240052 Free PMC article.
Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins).
Mosbah H, Donadille B, Vatier C, Janmaat S, Atlan M, Badens C, Barat P, Béliard S, Beltrand J, Ben Yaou R, Bismuth E, Boccara F, Cariou B, Chaouat M, Charriot G, Christin-Maitre S, De Kerdanet M, Delemer B, Disse E, Dubois N, Eymard B, Fève B, Lascols O, Mathurin P, Nobécourt E, Poujol-Robert A, Prevost G, Richard P, Sellam J, Tauveron I, Treboz D, Vergès B, Vermot-Desroches V, Wahbi K, Jéru I, Vantyghem MC, Vigouroux C. Mosbah H, et al. Among authors: ben yaou r. Orphanet J Rare Dis. 2022 Apr 19;17(Suppl 1):170. doi: 10.1186/s13023-022-02308-7. Orphanet J Rare Dis. 2022. PMID: 35440056 Free PMC article.
49 results