Mitochondrial DNA and Disease
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A 67-YEar-Old Man with Multiple Intracranial Lesions
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Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
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Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
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Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
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Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
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A Woman in Her 60s with Chronic Meningitis from Aspergillus
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Clinicopathologic Conference, Parainfectious Encephalomyelitis Associated with Systemic Mycoplasma Infection
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Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
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Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Congenital Lymphocytic Choriomeningitis Virus Infection: Spectrum of Disease
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Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
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Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
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SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
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Clinical and Neuroradiologic Features of Acute Disseminated Encephalomyelitis in Children
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Retinocochleocerebral Vasculopathy
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Susac Syndrome
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Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
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Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
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Niemann-Pick Disease Type C from Bench to Bedside
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Cytomegalovirus Encephalitis
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Lyme Neuroborreliosis
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Methylmercury Poisoning:Long-Term Clinical, Radiological, Toxicological, and Pathological Studies of an Affected Family
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MR Findings in Seven Patients with Organic Mercury Poisoning (Minamata Disease)
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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Angelman Syndrome: Clinical Profile
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Sarcoidosis of the Nervous System, A Clinical Approach
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Reversal of a Neurologic Paraneoplastic Syndrome with Octreotide (Sandostatin) in a Pt with Glucagonoma
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Progressive Rubella Panencephalitis
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Radiation-Induced Dementia in Patients Cured of Brain Metastases
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Clinical & Magnetic Resonance Features of Primary Intracranial Arachnoid Cysts
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Partial Dorsal Mesencephalic Hemorrhages:Report of Three Cases
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Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
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Hydrocephalic Dementia in Pagets Disease of the Skull:Treatment by Ventriculoatrial Shunt
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Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients
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Alcoholism
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Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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Wernekinck Commissure Syndrome
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
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Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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A Middle-Aged Man with Progressive Gait Abnormalities
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Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
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