Neurologic Complications of Babesiosis, United States, 2011-2021
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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Heterogeneity of Coenzyme Q10 Deficiency
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Encephalopathy in Infants & Children With Chronic Renal Disease
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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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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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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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Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
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Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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A Woman in Her 60s with Chronic Meningitis from Aspergillus
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CNS Posttransplant Lymphoproliferative Disorder
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A 57-year-old Woman with Ataxia and Oscillopsia
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A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
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Extraintestinal Manifestations of Coeliac Disease
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Legionella
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Intracranial Neoplasms and Paraneoplastic Disorders, Hemangioblastoma of the Cerebellum
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Degenerative Diseases of the Nervous System, Multiple System Atrophy
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Degenerative Diseases of the Nervous System, Friedreich Ataxia
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Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease
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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Clinicopath Conf, Intravascular Large-B-Cell Lympoma
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Primary Central Nervous System Post-Transplantation Lymphoproliferative Disorder
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Second Consensus Statement on the Diagnosis of Multiple System Atrophy
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Spectrum of Neurological Syndromes Associated with Glutamic Acid Decarboxylase Antibodes: Diagnostic Clues for this Association
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Epilepsy Syndromes in Infancy
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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Mitochondrial DNA Polymerase-y and Human Disease
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Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
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Mitochondrial Respiratory-Chain Diseases
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Clinical Manifestations of Sarin Nerve Gas Exposure
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Neurological Presentation of Fabry's Disease in a 52 Year Old Man
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Mycoplasma Pneumoniae Encephalitis in Childhood
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Neurologic Complications in Children with Enterovirus 71 Infection
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Prader-Willi and Angelman Syndromes
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Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
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Niemann-Pick Disease Type C from Bench to Bedside
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Cytomegalovirus Encephalitis
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Mitochondrial DNA and Disease
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Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
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Acute Sensory Neuronopathy:Report of a Child with Remarkable Clinical Recovery
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Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
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Arginase Deficiency Presenting as Cerebral Palsy
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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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