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Page 1
[Myotonia syndromes].
Pouget J, Desnuelle C. Pouget J, et al. Among authors: desnuelle c. Rev Prat. 1988 Oct 6;38(22):1546-51. Rev Prat. 1988. PMID: 3060972 Review. French. No abstract available.
[Hypermobility syndrome].
Serratrice G, Pouget J, Desnuelle C. Serratrice G, et al. Among authors: desnuelle c. Rev Rhum Mal Osteoartic. 1989 Dec;56(12):885. Rev Rhum Mal Osteoartic. 1989. PMID: 2617100 French. No abstract available.
Dehydroepiandrosterone for myotonic dystrophy type 1.
Pénisson-Besnier I, Devillers M, Porcher R, Orlikowski D, Doppler V, Desnuelle C, Ferrer X, Bes MC, Bouhour F, Tranchant C, Lagrange E, Vershueren A, Uzenot D, Cintas P, Solé G, Hogrel JY, Laforêt P, Vial C, Vila AL, Sacconi S, Pouget J, Eymard B, Chevret S, Annane D. Pénisson-Besnier I, et al. Among authors: desnuelle c. Neurology. 2008 Aug 5;71(6):407-12. doi: 10.1212/01.wnl.0000324257.35759.40. Neurology. 2008. PMID: 18678823 Clinical Trial.
[Muscular scanning in polyarthritis and rheumatology].
Serratrice G, Acquaviva P, Schiano A, Pouget J, Desnuelle C. Serratrice G, et al. Among authors: desnuelle c. Rev Rhum Mal Osteoartic. 1985 May;52(5):313-5. Rev Rhum Mal Osteoartic. 1985. PMID: 3874417 French.
Gender as a Modifying Factor Influencing Myotonic Dystrophy Type 1 Phenotype Severity and Mortality: A Nationwide Multiple Databases Cross-Sectional Observational Study.
Dogan C, De Antonio M, Hamroun D, Varet H, Fabbro M, Rougier F, Amarof K, Arne Bes MC, Bedat-Millet AL, Behin A, Bellance R, Bouhour F, Boutte C, Boyer F, Campana-Salort E, Chapon F, Cintas P, Desnuelle C, Deschamps R, Drouin-Garraud V, Ferrer X, Gervais-Bernard H, Ghorab K, Laforet P, Magot A, Magy L, Menard D, Minot MC, Nadaj-Pakleza A, Pellieux S, Pereon Y, Preudhomme M, Pouget J, Sacconi S, Sole G, Stojkovich T, Tiffreau V, Urtizberea A, Vial C, Zagnoli F, Caranhac G, Bourlier C, Riviere G, Geille A, Gherardi RK, Eymard B, Puymirat J, Katsahian S, Bassez G. Dogan C, et al. Among authors: desnuelle c. PLoS One. 2016 Feb 5;11(2):e0148264. doi: 10.1371/journal.pone.0148264. eCollection 2016. PLoS One. 2016. PMID: 26849574 Free PMC article.
[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases].
Humbertclaude V, Hamroun D, Picot MC, Bezzou K, Bérard C, Boespflug-Tanguy O, Bommelaer C, Campana-Salort E, Cances C, Chabrol B, Commare MC, Cuisset JM, de Lattre C, Desnuelle C, Echenne B, Halbert C, Jonquet O, Labarre-Vila A, N'guyen-Morel MA, Pages M, Pepin JL, Petitjean T, Pouget J, Ollagnon-Roman E, Richelme C, Rivier F, Sacconi S, Tiffreau V, Vuillerot C, Béroud C, Tuffery-Giraud S, Claustres M. Humbertclaude V, et al. Among authors: desnuelle c. Rev Neurol (Paris). 2013 Aug-Sep;169(8-9):583-94. doi: 10.1016/j.neurol.2013.04.004. Epub 2013 Aug 14. Rev Neurol (Paris). 2013. PMID: 23954141 French.
[Mitochondrial and ocular myopathies (62 cases)].
Serratrice G, Pellissier JF, Desnuelle C, Pouget J. Serratrice G, et al. Among authors: desnuelle c. Rev Neurol (Paris). 1991;147(6-7):474-5. Rev Neurol (Paris). 1991. PMID: 1962053 French.
[Slowly progressive myopathy with accumulation of tubular aggregates].
Figarella-Branger D, Pellissier JF, Perez-Castillo AM, Desnuelle C, Pouget J, Serratrice G. Figarella-Branger D, et al. Among authors: desnuelle c. Rev Neurol (Paris). 1991;147(8-9):586-94. Rev Neurol (Paris). 1991. PMID: 1962068 Review. French.
212 results