Ghent University Academic Bibliography

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Your filters: cql: author="Peeters, Karin" or (type exact bookEditor and editor="Peeters, Karin")

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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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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 (UGent) , Rik Vandenberghe, Stephanie Philtjens, Marleen Van den Broeck, Karin Peeters, et al.

(2018) NEUROBIOLOGY OF AGING. 67. p.84-94
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Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion

Sara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, Kristel Sleegers, Jan De Bleecker (UGent) , Anne Sieben (UGent) , Rik Vandenberghe, Tim Van Langenhove (UGent) , Jonathan Baets, Olivier Deryck, et al.

(2017) JAMA NEUROLOGY. 74(4). p.445-452
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Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

Tobi Van den Bossche, Kristel Sleegers, Elise Cuyvers, Sebastiaan Engelborghs, Anne Sieben (UGent) , Arne De Roeck, Caroline Van Cauwenberghe, Steven Vermeulen, Marleen Van den Broeck, Annelies Laureys, et al.

(2016) NEUROLOGY. 86(23). p.2126-2133
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Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort

Sara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, Sebastiaan Engelborghs, Anne Sieben (UGent) , Tim Van Langenhove (UGent) , Jan De Bleecker (UGent) , Jonathan Baets, Mathieu Vandenbulcke, Koen Van Laere, et al.

(2016) BRAIN. 139. p.452-467

Academic Bibliography

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

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

Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion

Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort

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