Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
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Relapsing-Remitting Severe Bickerstaffs Brainstem Encephalitis
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A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
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Acute Bulbar Palsy as a Variant of Guillain-Barre Syndrome
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Miller Fisher Syndrome with Positivity of Anti-GAD Antibodies
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Isolated Abducens Nerve Palsy as a Regional Variant of Guillain-Barre Syndrome
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Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
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Further Reg Var of Acute Polyneuro:Bifacial or 6th Nerve Paresis, Lumbar Polyrad & Ataxia/Phary Cervical-Brachial Wkness
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Serum anti-GQ1b IgG antibody is Associated with Ophthalmoplegia in Miller Fisher Syndrome and Guillain-Barre Syndrome: Clinical and Immunohistochemical Studies
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Miller Fisher Syndrome Associated with Q Fever
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Relapsing Ophthalmoparesis-Sensory Neuropathy Syndrome
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Brainstem Encephalitis & The Syndrome Of Miller Fisher
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Fisher's Syndrome:A Pharmacological Study of the Pupils
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Tonic Pupils with Acute Ophthalmoplegic Polyneuritis
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Pseudointernuclear Ophthalmoplegia in Acute Idiopathic Polyneuritis (Fisher's Syndrome)
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An Unusual Variant of Acute Idiopathic Polyneuritis (Syndrome of Ophthalmoplegia, Ataxia, & Areflexia)
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An 8-Year-Old with Acute Onset Ataxia
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Epstein-Barr Virus Infections of the Nervous System
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Mycoplasma Pneumoniae Encephalitis in Childhood
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A Six-Year-Old Girl with Tick paralysis
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Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
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Lyme Neuroborreliosis
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Sarcoidosis of the Nervous System, A Clinical Approach
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Sensory Form of Acute Polyneuritis
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Sensory Ataxia, A Residual Disability of Guillain-Barre Syndrome
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Hypophosphatemia Mimicking Acute Guillain-Barre-Strohl Syndrome
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The Ataxic Form of Polyradiculoneuritis (Landry-Guillain-Barre Syndrome) Clinical & Pathologic Observations
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An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
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A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
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A Dizzy Architect
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Nonalcoholic Wernicke Encephalopathy
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Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
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Wall-Eyed Bilateral Internuclear Ophthalmoplegia by Ischemic Stroke
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Bilateral Claude Syndrome
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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A 58-year-old man with Progressive Ptosis and Walking Difficulty
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Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
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Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
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Diseases of the Nervous System Caused by Nutritional Deficiency, Wernicke-Korsakoff Syndrome (Thiamine B1) Deficiency
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Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin E Deficiency
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Legionella
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
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Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
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Central Nervous System Involvement in Whipple Disease
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
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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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