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Elisabeth Hens

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Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease(2021)
Auteurs: Stefanie Smolders, Stéphanie Philtjens, David Crosiers, Anne Sieben, Elisabeth Hens, Bavo Heeman, Sara Van Mossevelde, Philippe Pals, Bob Asselbergh, Roberto Dos Santos Dias, et al.
Premature termination codon mutations in ABCA7 contribute to Alzheimer's disease risk in Belgian patients(2021)
Auteurs: Liene Bossaerts, Elisabeth Hens, Bernard Hanseeuw, Rik Vandenberghe, Patrick Cras, Peter P De Deyn, Sebastiaan Engelborghs, Christine Van Broeckhoven
Pagina's: 307.e1-307.e7
Investigation of the role of matrix metalloproteinases in the genetic etiology of Alzheimer's disease(2021)
Auteurs: Julie Hoogmartens, Elisabeth Hens, Sebastiaan Engelborghs, Peter Paul De Deyn, Julie Van Der Zee, Christine Van Broeckhoven, Rita Cacace
Pagina's: 105.e1-105.e6
Contribution of homozygous and compound heterozygous missense mutations in VWA2 to Alzheimer's disease(2021)
Auteurs: Julie Hoogmartens, Elisabeth Hens, Sebastiaan Engelborghs, Rik Vandenberghe, Peter De Deyn, Rita Cacace, Christine Van Broeckhoven
Pagina's: 100.e17-100.e23
Amyloid-beta(1-43) cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations(2020)
Auteurs: Federica Perrone, Maria Bjerke, Elisabeth Hens, Anne Sieben, Maarten Timmers, Arne De Roeck, Rik Vandenberghe, Kristel Sleegers, Jean-Jacques Martin, Peter De Deyn, et al.