Ghent University Academic Bibliography

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

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Exome sequencing and multigene panel testing in 1,411 patients with adult-onset neurologic disorders

Nika Schuermans (UGent) , Hannah Verdin (UGent) , Jody Ghijsels (UGent) , Madeleine Hellemans (UGent) , Elke Debackere (UGent) , Elke Bogaert (UGent) , Sofie Symoens (UGent) , Leslie Naesens (UGent) , Elien Lecomte, David Crosiers, et al.

(2023) NEUROLOGY-GENETICS. 9(3).
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- Miscellaneous
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Editorial : prodromal Parkinson's disease

David Crosiers, Patrick Santens (UGent) and K. Ray Chaudhuri

(2021) FRONTIERS IN NEUROLOGY. 11.
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Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson’s disease

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.

(2021) ACTA NEUROPATHOLOGICA COMMUNICATIONS. 9(1).
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Homozygous and compound heterozygous rare variants in VPS13C contribute to Lewy body diseases

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.

(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

Academic Bibliography

Exome sequencing and multigene panel testing in 1,411 patients with adult-onset neurologic disorders

Editorial : prodromal Parkinson's disease

Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson’s disease

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

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