MR Neurography for the Diagnosis of Hypertrophic Neuropathies
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Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
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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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Hypertrophy of Multiple Cranial Nerves and Spinal Roots in Chronic Inflammatory Demyelinating Neuropathy
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PCR-Based Strategy for Dx of Hered Neuropathy with Liability to Pressure Palsies & Charcot-Marie-Tooth Dis Type 1A
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Inherited Primary Peripheral Neuropathies
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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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Strokelike Episodes in a Patient with Chronic Gait Abnormalities
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Cerebral White Matter Abnormalities in Patients with Charcot-Marie-Tooth Disease
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Man with Recurrent Paralysis and Cerebral White Matter Lesions
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Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
Neurol 79: e70-e72, Zhong, L.,et al, 2012
Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging
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The CNS Phenotype of X-Linked Charcot-Marie-Tooth Disease
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MR Imaging of the Cauda Equina in Hereditary Motor Sensory Neuropathies: Correlations with Sural Nerve Biopsy
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Compression of Spinal Cord and Cauda Equina in Charcot-Marie-Tooth Disease Type 1A
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Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
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