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Clinicopath Conf, Infantile Krabbe Disease
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Glycogen-Storage Disease Type II
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Aromatic L-Amino Acid Decarboxylase Deficiency
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
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Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
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The Cherry-red Spot-Myoclonus Syndrome
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Fatal Infantile Form of Muscle Phosphorylase Deficiency
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