CIDP, CMT1B, or CMT1B plus CIDP?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10072-020-04789-5.pdf
Reference10 articles.
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2. Ginsberg L, Malik O, Kenton AR et al (2004) Coexistent hereditary and inflammatory neuropathy. Brain 127:193–202. https://doi.org/10.1093/brain/awh017
3. DiVincenzo C, Elzinga CD, Medeiros AC, Karbassi I, Jones JR, Evans MC, Braastad CD, Bishop CM, Jaremko M, Wang Z, Liaquat K, Hoffman CA, York MD, Batish SD, Lupski JR, Higgins JJ (2014) The allelic spectrum of Charcot-Marie-Tooth disease in over 17,000 individuals with neuropathy. Mol Genet Genomic Med 2:522–529. https://doi.org/10.1002/mgg3.106
4. Fabrizi GM, Tamburin S, Cavallaro T, Cabrini I, Ferrarini M, Taioli F, Magrinelli F, Zanette G (2018) The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: an electrodiagnostic, nerve ultrasound and histological study. Clin Neurophysiol 129:21–32. https://doi.org/10.1016/j.clinph.2017.09.117
5. Sghirlanzoni A, Pareyson D, Balestrini MR, Bellone E, Berta E, Ciano C, Mandich P, Marazzi R (1992) HMSN III phenotype due to homozygous expression of a dominant HMSN II gene. Neurology 42(11):2201–2204
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