A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
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A 53-year-old Woman with Lower Extremity Paresthesias
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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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A 60-year-old man with arm weakness and numbness
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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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Chronic and Slowly Progressive Weakness of the Legs and Hands
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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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Autonomic Peripheral Neuropathy
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Hereditary Motor and Sensory Neuropathies
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Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging
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Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
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Detection of a Varient Protein in Hair:New Diagnostic Method in Portuguese Type Familial Amyloid Polyneuropathy
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Phenotypic Heterogen in Hered Neurop with Liability to Press Palsies Assoc with Chromosome 17p11. 2-12 Delet
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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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Hered Neuralgic Amyotrophy & Hered Neuropathy with Liability to Pressure Palsies:Distinct Clin, Electrophy & Genetic Entities
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Hereditary Neuralgic Amyotrophy & Hereditary Neuropathy with Liability to Pressure Palsies:Distinct Genetic Dis
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Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
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Corticosteroid-Responsive Dominantly Inherited Neuropathy in Childhood
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REcurrent Familial Brachial Plexus Palsies as the ONly Clinical Expression of'Tomaculous'Neuropathy
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Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
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Hereditary Neuropathy with Liability to Pressure Palsies
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Intensive Evaluation of Referred Unclassified Neuropathies Yields Improved Diagnosis
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Nerve-Growth Factor in Familial Dysautonomia
NEJM 295:671, Montalcini,R.L., 1976
Polyneroupathies of Undetermined Cause
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Complex Ataxia
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GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
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Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy
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LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Cardiac Dysfunction in Neuromuscular Diseases
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Facial Nerve is Liable to Pressure Palsy
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Is There a Familial Carpal Tunnel Syndrome? An Evaluation and Literature Review
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Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q
Neurol 46:1128-1132, Pellegrino,J.E.,et al, 1996
Restless Legs Syndrome:Clinicoetiologic Correlates
Neurol 47:1435-1441, Ondo,W.&Jankovic,J., 1996
Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994
Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992
Diagnostic Tests for Choreoacanthocytosis
Neurol 41:1000-1006, Feinberg,T.E.,et al, 1991
Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991
Welander's Distal Myopathy:Clinical Neurophysiol & Muscle Biopsy Obser in Young & Middle Aged Adults with Early Symptoms
JNNP 54:494-498, Borg,K., 1991