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The Tuberous Sclerosis Complex
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Spinal Muscular Atrophy
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts & Leukoencephalopathy (CADASIL)
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Few Psychological Consequences of Presymptomatic Testing for Huntington Disease
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The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
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Clinical Spectrum of CADASIL:A Study of 7 Families
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Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
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The Neurogenetic Genie:Testing for Huntington's Disease Mutation
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A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
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Attitudes Toward Direct Predictive Testing for the Huntington Disease Gene
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Presymptomatic Testing for Huntington's Disease in the United Kingdom
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The Psychological Consequences of Predictive Testing for Huntington's Disease
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Genetic Testing for Huntington's Disease
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Predictive Testing for Huntington's Disease, Progress and Problems
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Uptake of Presymptomatic Predictive Testing for Huntington's Disease
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Presymptomatic Detection of Huntington's Chorea
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Use of L-Dopa in the Detection of Presymptomatic Huntington's Chorea
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