1: DiVincenzo C et al. The alle\/ic spectrum of Charcot-Marie-Tooth disease in over 17’000 idividua\/s with neuropathy. Molecular Genetics & Genomic Medicine. 2014:522-9.<\/p>\n
2: Shy ME et al. Neuropathy progression in Charcot-Marie-Tooth disease type 1A. Neurology 2008;70:378-83.<\/p>\n
3: Bird TD. Charcot-Marie-Tooth Neuropathy Type 1. ln: Pagan RA, Adam MP, Ardinger HH et al. editors. GeneReviews\u00ae . Seattle (WA): University of Washington, Seattle; 1993-2015. 1998 Aug 31 [updated 2015 Mar 26].<\/p>\n
4: Brennan KM, Bai Y, Shy ME. Demye\/inating CMT–what’s known, what’s new and what’s in store? Neurosci Lett. 2015;596:14-26.<\/p>\n
5: Saporta AS, Sottile SL, Miller LJ, et al. Charcot-Marie-Tooth disease subtypes and genetic testing strategies. Ann Neural. 2011 ;69:22-33<\/p>\n
6: Grandis M, Shy ME. Current Therapy for Charcot-Marie-Tooth Disease. Curr Treat Options Neural. 2005;7:23-31.<\/p>\n
7: Schr\u00f4der JM. Neuropathology of Charcot-Marie-Tooth and related disorders. Neuromolecular Med. 2006;8:23-42.<\/p>\n
8: Franssen H. Electrophysiology in demyelinating polyneuropathies. Expert Rev Neurother. 2008;8:417-31.<\/p>\n
9: Shy ME, Blake J, Krajewski K et al. Reliability and validity of the GMT neuropathy score as a measure of disability. Neuro\/ogy. 2005;64: 1209-14.<\/p>\n
10: Graham RC, Hughes RA. A modified peripheral neuropathy scale: the Overa\/1 Neuropathy Limitations Scale. J Neural Neurosurg Psychiatry. 2006;77:973-6.<\/p>\n","protected":false},"excerpt":{"rendered":"
1: DiVincenzo C et al. The alle\/ic spectrum of Charcot-Marie-Tooth disease in over 17’000 idividua\/s with neuropathy. Molecular Genetics & Genomic Medicine. 2014:522-9. 2: Shy ME et al. Neuropathy progression in Charcot-Marie-Tooth disease type 1A. Neurology 2008;70:378-83. 3: Bird TD. Charcot-Marie-Tooth Neuropathy Type 1. ln: Pagan RA, Adam MP, Ardinger HH et al. editors. GeneReviews\u00ae…
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