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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Spinal Muscular Atrophy
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Molybdenum Cofactor Deficiency
Neurol 85:e175-e178, Nagappa, M.,et al, 2015
A 52-year-old Woman with Progressive Proximal Weakness
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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The Muscular Dystrophies
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Analysis of Prenatal and Gestational Care Given to Women with Epilepsy
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Practice Parameter,Management Issues for Women with Epilepsy (Summary Statement)
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X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
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Hereditary Spastic Paraplegia:Advances in Genetic Research
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
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Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
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Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
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Dystrophinopathy in Isolated Cases of Myopathy in Females
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Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
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Distinction of Becker from Limb-Girdle Muscular Dystrophy by Means of Dystrophin cDNA Probes
Lancet 1:466-468, Norman,A.,et al, 1989
Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
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Prenatal Diagnosis of Cockayne's Syndrome
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Neurological Findings in Patients with the Fragile-X Syndrome
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