Familial Cavernous Angiomas
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A 51-Year-Old Woman with Abnormal Corups Callosum Signal
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A 14-Year-Old Girl with Headache, Seizures, and Confusion
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A 54-year-old man with Dyspnea and Muscle Weakness
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A Teenager with Persistent Headache
Neurol 92:e1526-e1531, Hu, Y.,et al, 2019
Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Pseudotumor Cerebri
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Clinical and Biomarker Changes in Dominantly Inherited Alzheimers Disease
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LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
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Genetic Aspects of Alzheimer Disease
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Association of Parental Dementia With Cognitive and Brain MRI Measures in Middle-Aged Adults
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Biochemical Markers in Persons With Preclinical Familial Alzheimer Disease
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Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
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Identification of New Presenilin Gene Mutations in Early-Onset Familial Alzheimer Disease
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Association Between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
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Serial Magnetic Resonance Imaging of Cerebral Atrophy in Preclinical Alzheimer's Disease
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Autosomal Dominant Myofibrillar Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy Linked to Chromosome 10q
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Familial Aggregation in Frontotemporal Dementia
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Hereditary Form of Parkinsonism-Dementia
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Factor V Leiden Mutation is a Risk Factor for Cerebral Venous Thrombosis,A Case-Control Study of 55 Patients
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The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
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Clin Features of Early-Onset Alzheimer Disease in Large Kindred with an E280A Presenilin-1 Mutation
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Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
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Cerebral Venous Thrombosis:Role of Activated Protein C Resistance and Factor V Gene Mutation
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Clinical Genetic Analysis of Parkinson's Disease in the Contursi Kindred
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Familial Alzheimer's Disease
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Chromosome 14-Encoded Alzheimer's Disease:Genetic and Clinicopathological Description
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Familial Progressive Subcortical Gliosis
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Protein S Deficiency in Middle-Aged Women with Stroke
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Transmission and Age-At-Onset Patterns in Familial Alzheimer's Disease:Evidence for Heterogeneity
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A Large Kindred with Autosomal Dominant Parkinson's Disease
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Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
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Clinicopath Conf
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