APP Mutations in Cerebral Amyloid Angiopathy with or without Cortical Calcifications: Report of Three Families and a Literature Review

Iowa APP mutation-related hereditary cerebral amyloid angiopathy (CAA): A new family from Spain

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Iowa-type hereditary cerebral amyloid angiopathy in a Polish family

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Hereditary Cerebral Hemorrhage With Amyloidosis Associated With the E693K Mutation of APP

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Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies

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Cerebrospinal fluid amyloid β40is decreased in cerebral amyloid angiopathy

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