A 53-year-old Woman with Lower Extremity Paresthesias
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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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MR Neurography for the Diagnosis of Hypertrophic Neuropathies
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Chronic and Slowly Progressive Weakness of the Legs and Hands
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Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
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Clinical Reasoning: A 34-Year-Old Woman with Recurrent Bouts of Acral Paresthesias
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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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Finding the Causes of Inherited Neuropathies
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Hereditary Motor and Sensory Neuropathies
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NT-3 Promotes Nerve Regeneration and Sensory Improvement in CMT1A Mouse Models and in Patients
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Quality of Life in Patients with Charcot-Marie-Tooth Disease
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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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CMT with Pyramidal Features
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Disability and Quality of Life in Charcot-Marie-Tooth Disease Type 1
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MR Imaging of the Cauda Equina in Hereditary Motor Sensory Neuropathies: Correlations with Sural Nerve Biopsy
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Hypertrophy of Multiple Cranial Nerves and Spinal Roots in Chronic Inflammatory Demyelinating Neuropathy
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Compression of Spinal Cord and Cauda Equina in Charcot-Marie-Tooth Disease Type 1A
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The Roussy-Levy Family:From the Original Description to the Gene
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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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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
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Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
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Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
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Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
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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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De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
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Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
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Respiratory Muscle Weakness in Charcot-Marie-Tooth Disease, A Field Study
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Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
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Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
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Respiratory Muscle Dysfunction in Hereditary Motor Sensory Neuropathy, Type I
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Hereditary Motor & Sensory Neuropathy, X-Linked:A Half Century Follow-Up
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Exacerbation of Charcot-Marie-Tooth Disease in Pregnancy
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Pattern Reversal Visual Evoked Potentials
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Central Vestibular Involvement in Peroneal Muscle Atrophy:A Preliminary Report
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Multiple Endocrine Neoplasia, Type 2b:Phenotype Recognition; Neurological Features & Their Pathological Basis
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Charcot-Marie-Tooth Disease Associated With"Essential Tremor"
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Neurotoxicity of Commonly Used Antineoplastic Agents
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Epidemiology of Motor-Neuron Diseases
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Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
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Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
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Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024
A 48-Year-Old Man With Spasticity and Progressive Ataxia
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