Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
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Conventional MRI and NOTCH3 Gene Screening in Sporadic CADASIL
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts & Leukoencephalopathy (CADASIL)
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Genetic Screening for a Single Common LRRK2 Mutation in Familial Parkinson's Disease
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Clinical Spectrum of CADASIL:A Study of 7 Families
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Molecular Genetics in Neurology
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