Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
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Clinical Genetics in Neurological Disease
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Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
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De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
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Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
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A 53-year-old Woman with Lower Extremity Paresthesias
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Chronic and Slowly Progressive Weakness of the Legs and Hands
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Clinical Reasoning: A 34-Year-Old Woman with Recurrent Bouts of Acral Paresthesias
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Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
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Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging
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Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
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Exacerbation of Charcot-Marie-Tooth Disease in Pregnancy
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Neurotoxicity of Commonly Used Antineoplastic Agents
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