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A Multidisciplinary Study of Patients with Early-Onset PD with and Without Parkin Mutations
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Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients
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Amyotrophic Lateral Sclerosis
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The Tuberous Sclerosis Complex
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Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Clinical Consequences of Isolating the Gene for Huntington's Disease
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