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A Young Man with Progressive Vision and Hearing Loss
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Neurosyphilis
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Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
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A Rare Cause of Gait Ataxia
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Clinical Reasoning: Seizures in a Child With Sensorineural Deafness and Agitation
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Profound Deafness in Childhood
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Cogan Syndrome
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Neurofibromatosis Type 2
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Clinicopath Conf., Leighs syndrome, Intraventricular Hemorrhage and Periventricular Leukomalacia
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Sudden Deafness From Stroke
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Neurobrucellosis:Clinical and Neuroimaging Correlation
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Sudden Unilateral Deafness Due to a Right Vertebral Artery Dissection
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Sudden Sensorineural Hearing Loss Associated with Herpes Simplex Virus Type 1 Infection
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Bilateral Sudden Deafness as a Prodrome of Anterior Inferior Cerebellar Artery Infarction
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Meningeal Carcinomatosis Manifested as Bilateral Progressive Sensorineural Hearing Loss
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Retinocochleocerebral Vasculopathy
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Spontaneous Intracranial Hypotension: Clinical and Magnetic Resonance Imaging
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Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
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On Politics and Health:An Epidemic of Neurologic Disease in Cuba
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The Landau-Kleffner Syndrome
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Susac's Syndrome:Triad of Microangiopathy of the Brain and Retina with Hearing Loss in Young Women
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Magnetic Resonance Imaging of Brain and the Neuromotor Disorder in Endemic Cretinism
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Sudden Hearing Loss as the Initial Monosymptom of Multiple Sclerosis
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The Landau-Kleffner Syndrome or Acquired Aphasia with Convulsive Disorder
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Small Infarctions of Cochlear, Retinal, and Encephalic Tissue in Young Women
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Cochlear Implants Prove Their Worth
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Sudden Deafness after Dental Surgery
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Magnetic Resonance Imaging of the Brain in Congenital Rubella Virus and Cytomegalovirus Infections
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Neurologic Manifestations of Giant Cell Arteritis
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Acute Sensorineural Deafness in Lassa Fever
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Cranial Nerve Deficit:A Clue to the Diagnosis of Ethylene Glycol Poisoning
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Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
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