A Familial Syndrome of Dystonia, Blepharospasm, and Pigmentary Retinopathy
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Behcet Disease
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003
Mitochondrial DNA and Disease
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
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Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992
Neurological Complications of Acquired Immune Deficiency Syndrome:Analysis of 50 Patients
Ann Neurol 14:403-418, Snider,W.D.,et al, 1983
Leber's Idiopathic Stellate Retinopathy
Am J Ophthalmol 93:96-101, Carroll,D.M.,et al, 1982
Central Nervous System Manifestations of Periarteritis Nodosa
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