Ghent University Academic Bibliography

Your filters: cql: author="De Deyn, Peter P." or (type any "bookEditor issueEditor" and editor="De Deyn, Peter P.")

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Rare ABCA7 mutations in Alzheimer’s disease and cerebral amyloid angiopathy pathology

Elisabeth Hendrickx Van de Craen, Liene Bossaerts, Anne Sieben, Tobi Van den Bossche, Maria Bjerke, Bernard Hanseeuw, Bruno Bergmans (UGent) , Rik Vandenberghe, Peter P. De Deyn, Patrick Cras, et al.

(2026) NEUROBIOLOGY OF AGING. 160. p.33-46
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Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum

Helena Gossye, Sarah Van Mossevelde (UGent) , Anne Sieben, Maria Bjerke, Elisabeth Hendrickx Van de Craen, Julie van der Zee, Peter P. De Deyn, Jan De Bleecker (UGent) , Jan Versijpt, Jenneke van den Ende, et al.

(2023) BRAIN. 146(4). p.1624-1636
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No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers

Cemile Koçoğlu, Helena Gossye, Lubina Dillen, Sara Van Mossevelde, Jan De Bleecker (UGent) , Rik Vandenberghe, Peter P. De Deyn, Kristel Sleegers, Patrick Cras, Sebastiaan Engelborghs, et al.

(2021) NEUROBIOLOGY OF AGING. 97. p.145.e1-145.e4
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Amyloid-β1–43 cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations

Federica Perrone, Maria Bjerke, Elisabeth Hens, Anne Sieben, Maarten Timmers, Arne De Roeck, Rik Vandenberghe, Kristel Sleegers, Jean-Jacques Martin, Peter P. De Deyn, et al.

(2020) ALZHEIMERS RESEARCH & THERAPY. 12(1).
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Evaluating the applicability of mouse SINEs as an alternative normalization approach for RT-qPCR in brain tissue of the APP23 model for Alzheimer’s disease

Jana Janssens, René Crans, Kathleen Van Craenenbroeck (UGent) , Jo Vandesompele (UGent) , Christophe Stove (UGent) , Debby Van Dam and Peter P. De Deyn

(2019) JOURNAL OF NEUROSCIENCE METHODS. 320. p.128-137
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Alzheimer’s disease and driving : review of the literature and consensus guideline from Belgian dementia experts and the Belgian road safety institute endorsed by the Belgian Medical Association

Jan Versijpt, Mark Tant, Ingo Beyer, Jean-Christophe Bier, Patrick Cras, Peter P. De Deyn, Patrick De Wit, Olivier Deryck, Bernard Hanseeuw, Margareta Lambert, et al.

(2017) ACTA NEUROLOGICA BELGICA. 117(4). p.811-819
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A general decline in cerebrospinal fluid flow : an overlooked risk factor for glaucoma?

Peter Wostyn, Veva De Groot, Debby Van Dam, Kurt Audenaert (UGent) and Peter P. De Deyn

(2016) JOURNAL OF NEURO-OPHTHALMOLOGY. 36(2). p.227-228
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Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains

Jonathan Janssens, Stephanie Philtjens, Gernot Kleinberger, Sara Van Mossevelde, Julie van der Zee, Rita Cacace, Sebastiaan Engelborghs, Anne Sieben, Julia Banzhaf-Strathmann, Lubina Dillen, et al.

(2015) ACTA NEUROPATHOLOGICA COMMUNICATIONS. 3.
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Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

Marc Cruts, Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, Hans Wils, Daniel Pirici, Rosa Rademakers, Rik Vandenberghe, Bart Dermaut (UGent) , Jean-Jacques Martin, et al.

(2006) NATURE. 442(7105). p.920-924

Academic Bibliography

Rare ABCA7 mutations in Alzheimer’s disease and cerebral amyloid angiopathy pathology

Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum

No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers

Amyloid-β1–43 cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations

Evaluating the applicability of mouse SINEs as an alternative normalization approach for RT-qPCR in brain tissue of the APP23 model for Alzheimer’s disease

Alzheimer’s disease and driving : review of the literature and consensus guideline from Belgian dementia experts and the Belgian road safety institute endorsed by the Belgian Medical Association

A general decline in cerebrospinal fluid flow : an overlooked risk factor for glaucoma?

Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

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