Ghent University Academic Bibliography

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Subclinical epileptiform activity in the Alzheimer continuum : association with disease, cognition and detection method

Amber Nous, Laura Seynaeve, Odile Feys, Vincent Wens, Xavier De Tiège, Pieter van Mierlo (UGent) , Amir Ghasemi Baroumand (UGent) , Koenraad Nieboer, Gert-Jan Allemeersch, Shana Mangelschots, et al.

(2024) ALZHEIMERS RESEARCH & THERAPY. 16(1).
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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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Hippocampal sclerosis in frontotemporal dementia : when vascular pathology meets neurodegeneration

Anne Sieben, Tim Van Langenhove (UGent) , Yannick Vermeiren, Helena Gossye, Marleen Praet, Dimitri Vanhauwaert, Celine Cousaert, Sebastiaan Engelborghs, Robrecht Raedt (UGent) , Paul Boon (UGent) , et al.

(2021) JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. 80(4). p.313-324
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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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Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export

Shaun Martin, Stefanie Smolders, Chris Van den Haute, Bavo Heeman, Sarah van Veen, David Crosiers, Igor Beletchi, Aline Verstraeten, Helena Gossye, Geraldine Gelders, et al.

(2020) ACTA NEUROPATHOLOGICA. 139(6). p.1001-1024
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Loss of DPP6 in neurodegenerative dementia : a genetic player in the dysfunction of neuronal excitability

Rita Cacace, Bavo Heeman, Sara Van Mossevelde, Arne De Roeck, Julie Hoogmartens, Peter De Rijk, Helena Gossye, Kristof De Vos, Wouter De Coster, Mojca Strazisar, et al.

(2019) ACTA NEUROPATHOLOGICA. 137(6). p.901-918
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Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion

Jelle van den Ameele (UGent) , Ivana Jedlickova, Anna Pristoupilova, Anne Sieben, Sara Van Mossevelde, Chantal Ceuterick-de Groote, Helena Hůlková, Radoslav Matej, Alfred Meurs, Christine Van Broeckhoven, et al.

(2018) NEUROLOGY. 90(8). p.e658-e663
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An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease

Arne De Roeck, Lena Duchateau, Jasper Van Dongen, Rita Cacace, Maria Bjerke, Tobi Van den Bossche, Patrick Cras, Rik Vandenberghe, Peter P De Deyn, Sebastiaan Engelborghs, et al.

(2018) ACTA NEUROPATHOLOGICA. 135(6). p.827-837
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Extended FTLD pedigree segregating a Belgian GRN-null mutation : neuropathological heterogeneity in one family

Anne Sieben, Sara Van Mossevelde, Eline Wauters, Sebastiaan Engelborghs, Julie van der Zee, Tim Van Langenhove (UGent) , Patrick Santens (UGent) , Marleen Praet, Paul Boon (UGent) , Marijke Miatton (UGent) , et al.

(2018) ALZHEIMERS RESEARCH & THERAPY. 10.
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Clinical variability and onset age modifiers in an extended Belgian GRN founder family

Eline Wauters, Sara Van Mossevelde, Kristel Sleegers, Julie van der Zee, Sebastiaan Engelborghs, Anne Sieben, Rik Vandenberghe, Stephanie Philtjens, Marleen Van den Broeck, Karin Peeters, et al.

(2018) NEUROBIOLOGY OF AGING. 67. p.84-94

Academic Bibliography

Subclinical epileptiform activity in the Alzheimer continuum : association with disease, cognition and detection method

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

Hippocampal sclerosis in frontotemporal dementia : when vascular pathology meets neurodegeneration

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

Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export

Loss of DPP6 in neurodegenerative dementia : a genetic player in the dysfunction of neuronal excitability

Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion

An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease

Extended FTLD pedigree segregating a Belgian GRN-null mutation : neuropathological heterogeneity in one family

Clinical variability and onset age modifiers in an extended Belgian GRN founder family

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