Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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A Teenager with Shortness of Breath and Difficulty Walking
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A 29-Year-Old Man with Fevers and Rapidly Progressive Cranial Neuropathies
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Homonymous Hemianopia with Normal Magnetic Resonance Imaging
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A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
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An Unusual Fundus Finding in a Teenage Girl
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Clinicopathologic Conference, Granulomatous Amebic Encephalitis and Sarcoidosis (Inactive)
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Cyclical Konzo Epidemics and Climate Variability
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Enterovirus Vaccines for an Emerging Cause of Brain-Stem Encephalitis
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
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Inherited Metabolic Diseases of the Nervous System, Infantile Niemann-Pick Disease
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Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
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Clinicopathologic Conference, Glioblastonoma, WHO grade IV of IV, with Methylation of the MGMT Promoter
NEJM 366:2112-2120, Case 17-2012, 2012
A Strange Case of Waitress Headache
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Downbeat Nystagmus: Aetiology and Comorbidity in 117 Patients
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q
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Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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Bilirubin Metabolism and Kernicterus
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Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy
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Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
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Cerebellar Infarction, Clinical and Anatomic Observations in 66 Cases
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Cytomegalovirus Ventriculoencephalitis in AIDS, A Syndrome with Distinct Clin & Path FEatures
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Cerebromeningeal Haemophagocytic Lymphohistiocytosis
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Acute Toxic Reaction to Carbamazepine:Clinical Effects and Serum Concentrations
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A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
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Central Nervous System Involvement in Von Hippel-Lindau Disease
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Nystagmus of Pelizaeus-Merzbacher Disease
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Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
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Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
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Joubert Syndrome:A Clinico-Radiological Study
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Friedreich Ataxia
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Paroxysmal Cerebellar Ataxia
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Chediak-Higashi Syndrome
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An Autosomal Dominant Syndrome of Hemiplegic Migraine, Nystagmus, & Tremor
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Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
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Familial Periodic Ataxia
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Dominant Spinopontine Atrophy
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The Cervical Myelopathy Associated with Rheumatoid Arthritis:Analysis of 32 Patients, with Two Post-mortem Cases
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Neurological Manifestations of Fabry Disease in Female Carriers
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Azorean Disease of the Nervous System
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Juvenile Diabetes Mellitus & Optic Atrophy
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