A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene.

Rossi, G; Giaccone, G; Maletta, R; Morbin, M; Capobianco, R; Mangieri, M; Giovagnoli, A R; Bizzi, A; Tomaino, C; Perri, M; Di Natale, M; Tagliavini, F; Bugiani, O; Bruni, A C

Rossi, G; Giaccone, G; Maletta, R; Morbin, M; Capobianco, R; Mangieri, M; Giovagnoli, A R; Bizzi, A; Tomaino, C; Perri, M; Di Natale, M; Tagliavini, F; Bugiani, O; Bruni, A C.

Affiliation

Rossi G; Division of Neuropathology and Neurology 5, Istituto Nazionale Neurologico Carlo Besta, Milan, Italy.

Neurology ; 63(5): 910-2, 2004 Sep 14.

Article in En | MEDLINE | ID: mdl-15365148

Subject(s)

Alzheimer Disease/genetics; Amyloid beta-Protein Precursor/genetics; Cerebral Amyloid Angiopathy/genetics; Cerebral Infarction/genetics; Mutation, Missense; Point Mutation; Alzheimer Disease/pathology; Amino Acid Substitution; Amyloid Precursor Protein Secretases; Amyloid beta-Protein Precursor/chemistry; Aspartic Acid Endopeptidases; Brain/pathology; Cerebral Amyloid Angiopathy/pathology; Cerebral Infarction/pathology; Codon/genetics; DNA Mutational Analysis; Disease Progression; Endopeptidases/metabolism; Female; Genes, Dominant; Humans; Italy; Magnetic Resonance Imaging; Male; Middle Aged; Pedigree

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Collection: 01-internacional Database: MEDLINE Main subject: Cerebral Infarction / Cerebral Amyloid Angiopathy / Amyloid beta-Protein Precursor / Point Mutation / Mutation, Missense / Alzheimer Disease Type of study: Risk_factors_studies Limits: Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Neurology Year: 2004 Document type: Article

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