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The prevalence of Charcot-Marie-Tooth (CMT) disease or hereditary motor and sensory neuropathy (HMSN) varies in different populations. While in some countries of Western Europe, the United States and… Continue Reading
Background/Aims: The prevalence of epilepsy in Algeria is unknown. The aims of this multicenter transversal study were to determine the national prevalence and clinical characteristics of epilepsy in… Continue Reading
OBJECTIVE Charcot-Marie-Tooth (CMT) disease 4B1 and 4B2 (CMT4B1/B2) are characterized by recessive inheritance, early onset, severe course, slowed nerve conduction, and myelin outfoldings. CMT4B3… Continue Reading
Introduction Le spectre clinique et genetique des neuropathies hereditaires liees aux mutations du gene GDAP1 est relativement large, comprenant des formes demyelinisantes et axonales de… Continue Reading