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Clinicopathological Conference
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Multiple Endocrine Neoplasia, Type 2b:Phenotype Recognition; Neurological Features & Their Pathological Basis
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Neurotoxicity of Commonly Used Antineoplastic Agents
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
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Stridor in Multiple System Atrophy
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GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
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Prodromal Symptoms of Multiple Sclerosis in Primary Care
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Clinicopathologic Conference, Botulism
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Multiple-System Atrophy
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Cardiovascular Dysfunction in Multiple Sclerosis
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Guillain-Barre Syndrome
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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
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Second Consensus Statement on the Diagnosis of Multiple System Atrophy
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Clinicopath Conf., Anti-MNDAR Antibody Mediated Paraneoplastic Limbic Encephalitis Associated With Ovarian Teratoma
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Anti-NMDA-Receptor Encephalitis: Case Series and Analysis of the Effects of Antibodies
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Paroxysmal Extreme Pain Disorder (Previously Familial Rectal Pain Syndrome)
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Pupil Findings in a Consecutive Series of 150 Patients with Generalised Autonomic Neuropathy
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Autonomic Dysfunction in Machado-Joseph Disease
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Autonomic Peripheral Neuropathy
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Clinicopath Conf, Multiple-System Atrophy
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Constipation in Neurological Diseases
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Sympathetic Cardioneuropathy in Dysautonomias
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Adult Botulism
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Consensus Statement on the Definition of Orthostatic Hypotension, Pure Autonomic Failure, and Multiple System Atrophy
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Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
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Clinical and Genetic Studies of Fatal Familial Insomnia
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Reflex Sympathetic Dystrophy
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Multiple System Atrophy presenting as Parkinsonism:Clinical Features and Diagnostic Criteria
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Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
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Growth Factors:Potential Therapeutic Applications in Neurology
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The Motor Disorder of Multiple System Atrophy
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Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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Fecal Incontinence
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A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
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Cranial Neuropathy Associated with Primary Amyloidosis
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Neurologic Aspects of Cobalamin Deficiency
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MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
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Abnormal Respiration and Sudden Death During Sleep in Multiple System Atrophy with Autonomic Failure
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The Remote Effects of Cancer on the Nervous System
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