Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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Toward Earlier Diagnosis of Amyotrophic Lateral Sclerosis, Revised Criteria
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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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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
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Herpes Simplex Encephalitis Treated with Acyclovir:Diagnosis and Long Term Outcome
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Multifocal Motor Neuropathy, Serum IgM Anti-GM1 Ganglioside Antibodies Detected Using Linkage of GM1 to ELISA Plates
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Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
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Multifocal Motor Neuropathy Presenting as Ophthalmoplegia
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Magnetic Resonance Imaging of the Brachial Plexus in Patients with Multifocal Motor Neuropathy
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Guillain-Barre Syndrome Following Allogeneic Bone Marrow Transplantation
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Adult Botulism
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Electrophysiologic Findings in Multifocal Motor Neuropathy
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Intravenous Immune Globulin Therapy for Neurologic Diseases
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ALS Standard of Care Consensus
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Sympathetic Cardioneuropathy in Dysautonomias
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ALS & Severe Cervical Spondylotic Myelopathy in Pt with a Posterior Fossa Archnoid Cyst:Diag Dilemma
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Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
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Multifocal Motor Neuropathy
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Chronic Inflammatory Demyelinating Polyradiculoneuropathy:Unusual Clinical Features and Therapeutic Responses
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Ten Steps in Characterizing and Diagnosing Patients with Peripheral Neuropathy
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Intravenous Immunoglobulin Treatment of Neurological Disease
JNNP 60:359-361, Otten,A.,et al, 1996
Pure Motor Hand Weakness
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Inclusion Body Myositis
JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996
Avoiding False Positive Diagnoses of Motor Neuron Disease:Lessons from the Scottish Motor Neuron Disease Register
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Diagnosing Motor Neurone Disease
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Childhood Leukemia:Central Nervous System Abnormalities During and After Treatment
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Multifocal Motor Neuropathy with Conduction Block and Campylobacter Jejuni
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From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
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Cytomegalovirus Encephalitis
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Diagnostic Guidelines in Central Nervous System Whipple's Disease
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Multifocal Demyelinating Motor Neuropathy:Pathologic Evidence of Inflammatory Demyelinasting Polyradiculoneuropathy
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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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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
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Acute, Painful, Pupil-involving Third Nerve Palsy in Chronic Inflammatory Demyelinating Polyneuropathy
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Improvement of Multifocal Motor Neuropathy During Long-Term Weekly Treatment with Human Immunoglobulin
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Multifocal Motor Neuropathy with Conduction Block:A Study of 24 Patients
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Diagnostic Yield of the Neurologic Assessment of the Developmentally Delayed Child
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Neurologic Aspects of Inflammatory Bowel Disease
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Acute Viral Encephalitis in Childhood
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Amyotrophic Lateral Sclerosis:Correlation of Clinical & MR Imaging Findings
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Lyme Neuroborreliosis
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The Electrophysiological Study of Diff Dx Between ALS & Cervical Spondylotic Myelopathy
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Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
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