Nerve Growth Factor (three parts)
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A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
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Strokelike Episodes in a Patient with Chronic Gait Abnormalities
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Clinical Reasoning: A Teenager with Left Arm Weakness
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MR Neurography for the Diagnosis of Hypertrophic Neuropathies
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Finding the Causes of Inherited Neuropathies
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Autonomic Peripheral Neuropathy
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NT-3 Promotes Nerve Regeneration and Sensory Improvement in CMT1A Mouse Models and in Patients
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Hereditary Motor and Sensory Neuropathies
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Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
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The CNS Phenotype of X-Linked Charcot-Marie-Tooth Disease
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Indications and Usefulness of Nerve Biopsy
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Clinical Spectrum of Chronic Acquired Demyelinating Polyneuropathies
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Hereditary Recurrent Focal Neuropathies, Clinical and Molecular Features
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Localization of the Giant Axonal Neuropathy Gene to Chromosome 16q24
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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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Detection of a Varient Protein in Hair:New Diagnostic Method in Portuguese Type Familial Amyloid Polyneuropathy
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Neurogenic Muscle Hypertrophy
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Clinicopath Conf
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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 Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
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Clin Electrophy & Molec Correl in 13 Families with Hered Neurop with Liabil to Press Palsies & Chromosome 17p11. 2 Deletion
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Liver Transplantation as a Treatment for Familial Amyloidotic Polyneuropathy
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DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
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Inherited Primary Peripheral Neuropathies
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Corticosteroid-Responsive Dominantly Inherited Neuropathy in Childhood
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Tangier Disease in a Black Patient:An Unusual Clinical Presentation
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Molecular Genetics of Amyloid Neuropathy in Europe
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Hereditary Sensory Neuropathy with Deafness:A Familial Multisystem Atrophy
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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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Refsum Disease
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Respiratory Muscle Dysfunction in Hereditary Motor Sensory Neuropathy, Type I
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Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
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Retinitis Pigmentosa
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Hereditary Motor & Sensory Neuropathy, X-Linked:A Half Century Follow-Up
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Ocular Complications of Tangier Disease
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