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Page 1
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
Bonne G, Mercuri E, Muchir A, Urtizberea A, Bécane HM, Recan D, Merlini L, Wehnert M, Boor R, Reuner U, Vorgerd M, Wicklein EM, Eymard B, Duboc D, Penisson-Besnier I, Cuisset JM, Ferrer X, Desguerre I, Lacombe D, Bushby K, Pollitt C, Toniolo D, Fardeau M, Schwartz K, Muntoni F. Bonne G, et al. Among authors: cuisset jm. Ann Neurol. 2000 Aug;48(2):170-80. Ann Neurol. 2000. PMID: 10939567
[Diagnostic approach of hyperCKemia in childhood].
Sabouraud P, Cuisset JM, Cances C, Chabrier S, Antoine JC, Richelme C, Chabrol B, Desguerre I, Rivier F; Commission Maladies Neuromusculaires de la Société Française de Neurologie Pédiatrique. Sabouraud P, et al. Among authors: cuisset jm. Arch Pediatr. 2009 Jun;16(6):678-80. doi: 10.1016/S0929-693X(09)74109-0. Arch Pediatr. 2009. PMID: 19541127 French. No abstract available.
[Multicentric study of medical care and practices in spinal muscular atrophy type 1 over two 10-year periods].
Barnérias C, Quijano S, Mayer M, Estournet B, Cuisset JM, Sukno S, Peudenier S, Laroche C, Chabrier S, Sabouraud P, Vuillerot C, Chabrol B, Halbert C, Cancès C, Beze-Beyrie P, Ledivenah A, Viallard ML, Desguerre I. Barnérias C, et al. Among authors: cuisset jm. Arch Pediatr. 2014 Apr;21(4):347-54. doi: 10.1016/j.arcped.2014.01.017. Epub 2014 Mar 12. Arch Pediatr. 2014. PMID: 24630620 French.
[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: cuisset jm. 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.
[Muscle biopsy in children: Usefulness in 2012].
Cuisset JM, Maurage CA, Carpentier A, Briand G, Thévenon A, Rouaix N, Vallée L. Cuisset JM, et al. Rev Neurol (Paris). 2013 Aug-Sep;169(8-9):632-9. doi: 10.1016/j.neurol.2012.11.011. Epub 2013 Aug 28. Rev Neurol (Paris). 2013. PMID: 23993361 French.
[Central manifestations of dystrophinopathies].
Cuisset JM, Rivier F. Cuisset JM, et al. Arch Pediatr. 2015 Dec;22(12 Suppl 1):12S58-62. doi: 10.1016/S0929-693X(16)30010-0. Arch Pediatr. 2015. PMID: 26773588 French.
[Neuropediatric approach to autism].
Cuisset JM, Joriot S, Auvin S, Gozé O, Medjkane F, Salloum A, Delion P, Vallée L. Cuisset JM, et al. Arch Pediatr. 2005 Dec;12(12):1734-41. doi: 10.1016/j.arcped.2005.09.016. Epub 2005 Oct 10. Arch Pediatr. 2005. PMID: 16219450 Review. French.
128 results