Anti-NMDA-Receptor Encephalitis: Case Series and Analysis of the Effects of Antibodies
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Aromatic L-Amino Acid Decarboxylase Deficiency
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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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GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
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Antibody-Mediated Encephalitis
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Paraneoplastic and Autoimmune Encephalitis
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Cardiovascular Dysfunction in Multiple Sclerosis
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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011
Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
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Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
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The Writing on the Wall
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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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Insular Involvement in Brain Infarction Increases Risk for Cardiac Arrhythmia and Death
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Autonomic Peripheral Neuropathy
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Prognositc Implications of Right-Sided Insular Damage, Cardiac Autonomic Derangement, and Arrhythmias After Acute Ischemic Stroke
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Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
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Clinicopath Conf, Multiple-System Atrophy
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Stimulus-Evoked Sinus Arrest in Severe Guillain-Barre Syndrome:A Case Report
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Clinical and Genetic Studies of Fatal Familial Insomnia
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Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
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Clin & Path Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simul Chronic Progressive MS
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Autonomic Involvement in Guillain-Barre Syndrome:A Review
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Supraventricular Tachycardia in Patients with Right Hemisphere Strokes
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Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
NEJM 326:444-449, Medori,R.,et al, 1992
Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
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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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A Prospective Study on Sudden Unexpected Death in Epilepsy
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Cardiovascular Autonomic Dysfunction in Guillain-Barre Syndrome, Therapeutic Implications of Swan-Ganz Monitoring
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Computed Tomography and Magnetic Resonance Imaging in Adult-Onset Leukodystrophy
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Fatal Familial Insomnia & Dysautonomia with Selective Degeneration of Thalamic Nuclei
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Clinicopathological Conference
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Sudden Unexpected Death Associated with Seizures:Analysis of 66 Cases
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Multiple Endocrine Neoplasia, Type 2b:Phenotype Recognition; Neurological Features & Their Pathological Basis
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Nerve-Growth Factor in Familial Dysautonomia
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The Neurological Sequelae of Electrical Injury
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