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Familial Recurrent Bell's Palsy with Ocular Motor Palsies
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Familial Amyloidosis with Cranial Neuropathy & Corneal Lattice Dystrophy
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Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
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Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
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Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
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Clinical Reasoning: A Teenager with Left Arm Weakness
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Inherited Metabolic Diseases of the Nervous System, Globoid Cell Leukodystrophy (Krabbe Disease, Galactocerebrosidase)
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Metabolic Disease and Stroke: MELAS
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Clin Electrophy & Molec Correl in 13 Families with Hered Neurop with Liabil to Press Palsies & Chromosome 17p11. 2 Deletion
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Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
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Central Core Disease, Clinical Features in 13 Patients
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Optic Neuritis in Familial MS
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Congenital Myotonic Dystrophy
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Neurological Manifestations of Fabry Disease in Female Carriers
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Duane Syndrome & Congential Upper-Limb Anomalies:A Familial Occurrence
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Juvenile Diabetes Mellitus & Optic Atrophy
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Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem
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Focusing on the Eye Signs of Alport Syndrome in a 40-Year-Old Man Who Previously Had a Kidney Transplant and Hearing Loss
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Bilateral Hearing Loss and Constricted Visual Fields
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A 22-Year-Old Man with Progressive Bilateral Visual Loss
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A 53-year-old Woman with Lower Extremity Paresthesias
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A 10-year-old boy with Bilateral Vision Loss
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Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
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Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
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A Neonate with Micrognathia and Hypotonia
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