Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Julie Hoogmartens"'
Publikováno v:
Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring, Vol 13, Iss 1, Pp n/a-n/a (2021)
Abstract Early‐onset Alzheimer's disease (EOAD) is generally known as a dominant disease due to highly penetrant pathogenic mutations in the amyloid precursor protein, presenilin 1 and 2. However, they explain only a fraction of EOAD patients (5% t
Externí odkaz:
https://doaj.org/article/a00e7f1e85d94724bdefd5a6b823b454
Publikováno v:
Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring, Vol 13, Iss 1, Pp n/a-n/a (2021)
Alzheimer's & Dementia : Diagnosis, Assessment & Disease Monitoring
Alzheimer's & Dementia : Diagnosis, Assessment & Disease Monitoring
Early-onset Alzheimer's disease (EOAD) is generally known as a dominant disease due to highly penetrant pathogenic mutations in the amyloid precursor protein, presenilin 1 and 2. However, they explain only a fraction of EOAD patients (5% to 10%). Fur
Autor:
Rita Cacace, Elisabeth Hens, Julie Hoogmartens, Sebastiaan Engelborghs, Rik Vandenberghe, Peter Paul De Deyn, Christine Van Broeckhoven
Publikováno v:
Alzheimer's & Dementia. 16
Autor:
Anne Sieben, Patrick Cras, Diederik Moechars, Jean-Jacques Martin, Sebastiaan Engelborghs, Elisabeth Hens, Rik Vandenberghe, Rita Cacace, Julie Hoogmartens, Christine Van Broeckhoven, Peter Paul De Deyn, Arjan Buist
Publikováno v:
Alzheimer's & Dementia. 16
Autor:
Julie Hoogmartens, Elisabeth Hens, Sebastiaan Engelborghs, Rik Vandenberghe, Peter-P. De Deyn, Rita Cacace, Christine Van Broeckhoven, P. Cras, J. Goeman, R. Crols, J.L. De Bleecker, T. Van Langenhove, A. Sieben, B. Dermaut, O. Deryck, B. Bergmans, J. Versijpt
Publikováno v:
Neurobiology of aging
Neurobiology of Aging, 99, 100.e17-100.e23. ELSEVIER SCIENCE INC
Neurobiology of Aging, 99, 100.e17-100.e23. ELSEVIER SCIENCE INC
Alzheimer's disease is the most frequent diagnosis of neurodegenerative dementia with early (≤65 years) and late (>65 years) onset ages in familial and sporadic patients. Causal mutations in 3 autosomal dominant Alzheimer genes, i.e. amyloid precur
Autor:
Nathalie Geerts, Sara Van Mossevelde, Sebastiaan Engelborghs, Julie Zee, Julie Hoogmartens, Peter Paul De Deyn, Christine Van Broeckhoven, Rik Vandenberghe, Tobi Van den Bossche, Rita Cacace, Kristel Sleegers
Publikováno v:
Alzheimer's & Dementia. 14