Interaction Between HLA-DR2 and Abnormal Brain MRI in Optic neuritis and Early MS
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Multiple Sclerosis
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Clumsiness, Confusion, Coma, and Valproate
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Behcet's Disease
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Diagnostic Aspects of Narcolepsy
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Optic Neuritis, Prognosis for Multiple Sclerosis from MRI, CSF, and HLA Findings
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Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
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Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation
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Adult-Onset Krabbe Disease with Mutation in the Galactocerebrosidase Gene, MRI of Corticospinal Tract Demyelin
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HLA Typing in Acute Optic Neuritis, Relation to MS & Magnetic Resonance Imaging Findings
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Adult-Onset Krabbe's Disease in Siblings with Novel Mutations in the Galactocerebrosidase Gene
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Clinical and Subclinical Neurological Involvement in Children of Conjugal Multiple Sclerosis Patients
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Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Myasthenia Gravis and Sarcoidosis:Report of 2 Cases
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Fisher Syndrome after Campylobacter Jejuni Enteritis:Human Leukocyte Antigen and the Bacterial Serotype
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Bilateral Simultaneous Optic Neuropathy in Adults:Clinical, Imaging, Serological, and Genetic Studies
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Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
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Dopamine, Dystonia, and the Deficient Co-Factor
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Inborn Errors of Urea Synthesis
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Postpartum Coma and Death Due to Carbamoyl-Phosphate Synthetase I Deficiency
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Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
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Human Leukocyte Antigens in Fisher's Syndrome
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Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
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Brain Imaging in Late-Onset CM2 Gangliosidosis
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Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
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Genetic Diagnosis of Gaucher's Disease
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Recurrent Transverse Myelitis, Myasthenia Gravis, and Autoantibodies
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Conjugal Multiple Sclerosis:Immunogenetic Characterization and Analysis of T-and B-Cell Reactivity to Myelin Proteins
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Psychiatric Disturbances in Metachromatic Leukodystrophy
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Idiopathic Childhoos Stroke is Associated with Human Leukocyte Antigen (HLA) -B51
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Polymorphonuclear Leukocytes and Monocytes/Macrophages in the Pathogenesis of Cerebral Ischemia and Stroke
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Central-Nervous-System Demyelination after Immunisation with Recombinant Hepatitis B Vaccine
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Central Nervous System Abnormalities in Lyme Neuroborreliosis
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Late Onset Globoid Cell Leukodystrophy
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Localization of Idiopathic Generalized Epilepsy on Chromosome 6p in Families of Juvenile Myoclonic epilepsy patients
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Fucosidosis Revisited:A Review of 77 Patients
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Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
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Conjugal Multiple Sclerosis:A Clinical and Laboratory Study
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Clinical Follow-Up and Immunogenetic Studies of 32 Patients with Eosinophilia-Myalgia Syndrome
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Progressive Neuropathy & Recurrent Myoglobinuria in a Child with Long-chain 3-Hydroxyacylcoenzyme A Dehydrogenase Defic
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Narcolspey
NEJM 323:389-394, Aldrich,M.S., 1990
Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus
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A Long-Term Prospective Study of Optic Neuritis:Evaluation of Risk Factors
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Risk Factors for Multiple Sclerosis:Race or Place? Editorial
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Cerebrotendinous Xanthomatosis:Clinical and MRI Study (A Case Report)
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Characteristics of Narcolepsy in Preteenaged Children
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Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990
Adult Phosphorylase b Kinase Deficiency
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