Ghent University Academic Bibliography

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Your filters: cql: author="Cras, Patrick" or (type any "bookEditor issueEditor" and editor="Cras, Patrick")

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- Journal Article
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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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- Journal Article
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Processing of laser-evoked potentials in patients with chronic whiplash-associated disorders, chronic fatigue syndrome, and healthy controls : a case–control study

Lisa Goudman, Liesbeth Daenen, Andre Mouraux, Jo Nijs, Patrick Cras, Nathalie Roussel, Maarten Moens, Iris Coppieters (UGent) , Eva Huysmans and Margot De Kooning

(2020) PAIN MEDICINE. 21(10). p.2553-2563
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Does motor cortex engagement during movement preparation differentially inhibit nociceptive processing in patients with chronic whiplash associated disorders, chronic fatigue syndrome and healthy controls? An experimental study

Lisa Goudman, André Mouraux, Liesbeth Daenen, Jo Nijs, Patrick Cras, Nathalie Roussel, Maarten Moens, Dorine Lenoir (UGent) , Iris Coppieters (UGent) , Eva Huysmans, et al.

(2020) JOURNAL OF CLINICAL MEDICINE. 9(5).
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Practices and opinions about disclosure of the diagnosis of Alzheimer’s disease to patients with MCI or dementia : a survey among Belgian medical experts in the field of dementia

Eric Mormont, Jean-Christophe Bier, Rose Bruffaerts, Patrick Cras, Peter De Deyn, Olivier Deryck, Sebastiaan Engelborghs, Mirko Petrovic (UGent) , Gaëtane Picard, Kurt Segers, et al.

(2020) ACTA NEUROLOGICA BELGICA. 120(5). p.1157-1163
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- Miscellaneous
- open access
Homozygous and compound heterozygous rare variants in VPS13C contribute to Lewy body diseases

Stefanie Smolders, Stéphanie Philtjens, David Crosiers, Anne Sieben (UGent) , Elisabeth Hens, Bavo Heeman, Sara Van Mossevelde, Philippe Pals, Bob Asselbergh, Roberto Dos Santos Dias, et al.

(2020) Research Square.
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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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Medische zorg toegediend door de arts in verband met toxicomanie : risico’s, gevolgen en mogelijke oplossingen

Jean Colin, Nick van Gelder, Patrick Cras, Marc De Hert and Freya Vander Laenen (UGent)

(2018) TIJDSCHRIFT VOOR GENEESKUNDE. 74(19). p.1274-1279
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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 (UGent) , 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.

Academic Bibliography

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

Processing of laser-evoked potentials in patients with chronic whiplash-associated disorders, chronic fatigue syndrome, and healthy controls : a case–control study

Does motor cortex engagement during movement preparation differentially inhibit nociceptive processing in patients with chronic whiplash associated disorders, chronic fatigue syndrome and healthy controls? An experimental study

Practices and opinions about disclosure of the diagnosis of Alzheimer’s disease to patients with MCI or dementia : a survey among Belgian medical experts in the field of dementia

Homozygous and compound heterozygous rare variants in VPS13C contribute to Lewy body diseases

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

Medische zorg toegediend door de arts in verband met toxicomanie : risico’s, gevolgen en mogelijke oplossingen

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

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