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

Year Number of Results
1993 1
2004 7
2005 4
2006 3
2007 4
2008 5
2009 6
2010 2
2011 2
2012 4
2013 3
2014 3
2015 10
2016 5
2017 4
2018 9
2019 5
2020 5
2021 10
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Search Results

83 results
Results by year
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Page 1
Dysferlinopathies.
Urtizberea JA, Bassez G, Leturcq F, Nguyen K, Krahn M, Levy N. Urtizberea JA, et al. Among authors: leturcq f. Neurol India. 2008 Jul-Sep;56(3):289-97. doi: 10.4103/0028-3886.43447. Neurol India. 2008. PMID: 18974555 Free article. Review.
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: leturcq f. 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.
Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase.
Tuffery-Giraud S, Béroud C, Leturcq F, Yaou RB, Hamroun D, Michel-Calemard L, Moizard MP, Bernard R, Cossée M, Boisseau P, Blayau M, Creveaux I, Guiochon-Mantel A, de Martinville B, Philippe C, Monnier N, Bieth E, Khau Van Kien P, Desmet FO, Humbertclaude V, Kaplan JC, Chelly J, Claustres M. Tuffery-Giraud S, et al. Among authors: leturcq f. Hum Mutat. 2009 Jun;30(6):934-45. doi: 10.1002/humu.20976. Hum Mutat. 2009. PMID: 19367636
[Sarcoglycanopathies: state of the art and therapeutic perspectives].
Fernández-Eulate G, Leturcq F, Laforêt P, Richard I, Stojkovic T. Fernández-Eulate G, et al. Among authors: leturcq f. Med Sci (Paris). 2020 Dec;36 Hors série n° 2:22-27. doi: 10.1051/medsci/2020243. Epub 2021 Jan 11. Med Sci (Paris). 2020. PMID: 33427632 Free article. Review. French.
Emery-Dreifuss Muscular Dystrophy.
Bonne G, Leturcq F, Ben Yaou R. Bonne G, et al. Among authors: leturcq f. 2004 Sep 29 [updated 2019 Aug 15]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. 2004 Sep 29 [updated 2019 Aug 15]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. PMID: 20301609 Free Books & Documents. Review.
Phenotypic Spectrum of Myopathies with Recessive Anoctamin-5 Mutations.
Vázquez J, Lefeuvre C, Escobar RE, Luna Angulo AB, Miranda Duarte A, Delia Hernandez A, Brisset M, Carlier RY, Leturcq F, Durand-Canard MC, Nicolas G, Laforet P, Malfatti E. Vázquez J, et al. Among authors: leturcq f. J Neuromuscul Dis. 2020;7(4):443-451. doi: 10.3233/JND-200515. J Neuromuscul Dis. 2020. PMID: 32925086
[Molecular bases of dystrophinopathies].
Leturcq F, Kaplan JC. Leturcq F, et al. J Soc Biol. 2005;199(1):5-11. doi: 10.1051/jbio:2005001. J Soc Biol. 2005. PMID: 16114258 Review. French.
X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterisation.
Barthélémy I, Calmels N, Weiss RB, Tiret L, Vulin A, Wein N, Peccate C, Drougard C, Beroud C, Deburgrave N, Thibaud JL, Escriou C, Punzón I, Garcia L, Kaplan JC, Flanigan KM, Leturcq F, Blot S. Barthélémy I, et al. Among authors: leturcq f. Skelet Muscle. 2020 Aug 7;10(1):23. doi: 10.1186/s13395-020-00239-0. Skelet Muscle. 2020. PMID: 32767978 Free PMC article.
[An overview of Duchenne muscular dystrophy in Martinique].
Sarrazin E, Valard-Giguet AG, Leturcq F, Bellance R. Sarrazin E, et al. Among authors: leturcq f. Med Sci (Paris). 2018 Nov;34 Hors série n°2:45-48. doi: 10.1051/medsci/201834s215. Epub 2018 Nov 12. Med Sci (Paris). 2018. PMID: 30418149 Free article. French. No abstract available.
83 results