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Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy.
Winkelmann J, Lin L, Schormair B, Kornum BR, Faraco J, Plazzi G, Melberg A, Cornelio F, Urban AE, Pizza F, Poli F, Grubert F, Wieland T, Graf E, Hallmayer J, Strom TM, Mignot E. Winkelmann J, et al. Among authors: mignot e. Hum Mol Genet. 2012 May 15;21(10):2205-10. doi: 10.1093/hmg/dds035. Epub 2012 Feb 9. Hum Mol Genet. 2012. PMID: 22328086 Free PMC article.
Genetic studies in the sleep disorder narcolepsy.
Kadotani H, Faraco J, Mignot E. Kadotani H, et al. Among authors: mignot e. Genome Res. 1998 May;8(5):427-34. doi: 10.1101/gr.8.5.427. Genome Res. 1998. PMID: 9582188 Free article. Review.
Narcolepsy and the HLA region.
Lin L, Hungs M, Mignot E. Lin L, et al. Among authors: mignot e. J Neuroimmunol. 2001 Jul 2;117(1-2):9-20. doi: 10.1016/s0165-5728(01)00333-2. J Neuroimmunol. 2001. PMID: 11431000 Review.
Narcolepsy-cataplexy associated with precocious puberty.
Plazzi G, Parmeggiani A, Mignot E, Lin L, Scano MC, Posar A, Bernardi F, Lodi R, Tonon C, Barbiroli B, Montagna P, Cicognani A. Plazzi G, et al. Among authors: mignot e. Neurology. 2006 May 23;66(10):1577-9. doi: 10.1212/01.wnl.0000216142.21375.71. Neurology. 2006. PMID: 16717224
Cataplexy features in childhood narcolepsy.
Serra L, Montagna P, Mignot E, Lugaresi E, Plazzi G. Serra L, et al. Among authors: mignot e. Mov Disord. 2008 Apr 30;23(6):858-65. doi: 10.1002/mds.21965. Mov Disord. 2008. PMID: 18307264
500 results