Mutational analysis of PMP22, GJB1 and MPZ in Greek Charcot-Marie-Tooth type 1 neuropathy patients von Karadima, G, Floroskufi, P, Koutsis, G, Vassilopoulos, D, Panas, M

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Mutational analysis of PMP22, EGR2, LITAF and NEFL in Greek Charcot-Marie-Tooth type 1 patients von Koutsis, G, Pandraud, A, Karadima, G, Panas, M, Reilly, MM, Floroskufi, P, Wood, NW, Houlden, H

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Hereditary neuropathy with liability to pressure palsies emerging during vincristine treatment von KALFAKIS, N, PANAS, M, KARADIMA, G, FLOROSKUFI, P, KOKOLAKIS, N, VASSILOPOULOS, D

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Four novel connexin 32 mutations in X-linked Charcot-Marie-Tooth disease with phenotypic variability von Karadima, G, Panas, M, Floroskufi, P, Kalfakis, N, Vassilopoulos, D

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Charcot-Marie-Tooth disease type 1A with central nervous system involvement in two generations von Panas, M, Karadima, G, Kalfakis, N, Floroskufi, P, Vassilopoulos, D

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A V38A mutation in X-linked Charcot-Marie-Tooth neuropathy with unusual clinical features von Karadima, Georgia, Panas, Marios, Floroskufi, Paraskewi, Kalfakis, Nikolaos, Vassilopoulos, Demetris

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Charcot-Marie-Tooth disease type 1A with central nervous system involvement in two generations von Panas, M, Karadima, G, Kalfakis, N, Floroskufi, P, Vassilopoulos, D

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