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Mostrando ítems 41-50 de 102
The A431E Presenilin 1 gene mutation associated with familial Alzheimer disease in individuals of Mexican descent: Evidence for a founder effect.
(AMER ASSN NEUROPATHOLOGISTS INC, 2003)
Female preclinical presenilin-1 mutation carriers unaware of their genetic status have higher levels of depression than their non-mutation carrying kin
(2004)
Objectives: To study depressive symptoms in preclinical presenilin-1 (PS1) related Alzheimer's disease. Methods: Participants were 33 Mexican women at risk for inheriting PS1 mutations who were not demented. They were ...
Female preclinical presenilin-1 mutation carriers unaware of their genetic status have higher levels of depression than their non-mutation carrying kin
(2004)
Objectives: To study depressive symptoms in preclinical presenilin-1 (PS1) related Alzheimer's disease. Methods: Participants were 33 Mexican women at risk for inheriting PS1 mutations who were not demented. They were ...
Doença de Alzheimer
(Associação Brasileira de Psiquiatria - ABP, 1999-10-01)
This paper concisely reviews the genetics of Alzheimer Disease (AD). So far, three different genes have been implicated in AD. Specifically, the gene that codes for APP - the amyloid beta precursor protein, which is ...
Insights into Alzheimer disease pathogenesis from studies in transgenic animal models
(Faculdade de Medicina / USP, 2011)
Alzheimer disease is the most common cause of dementia among the elderly, accounting for ~60-70% of all cases of dementia. The neuropathological hallmarks of Alzheimer disease are senile plaques (mainly containing p-amyloid ...
Clinical and molecular characterization of Alzheimer disease-type dementiain a large kingred in Antioquia, Colombia.
(Bogotá :Universidad de Antioquia,, 2019)
Clinical and molecular characterization of Alzheimer disease-type dementiain a large kingred in Antioquia, Colombia.
(Bogotá :Universidad de Antioquia,, 2019)
Brain Imaging and Blood Biomarker Abnormalities in Children With Autosomal Dominant Alzheimer Disease: A Cross-Sectional Study
(American Medical AssociationGrupo de Neurociencias de AntioquiaChicago, Estados Unidos, 2022)
A novel mutation Leu171Pro mutation in presenilin-1 gene in a Mexican family with early onset Alzheimer disease.
(1998)
A search for mutations in exons 6, 7, 9 and 12 of the PS1 gene in four Mexican families with Early-Onset (36-40 years) Alzheimer Disease yielded the discovery in one family of a T ? C mismatch in exon 7 which correspond ...