Researcher
Sebastiaan Engelborghs
Universitair Ziekenhuis Brussel
Statistics
5 papers found
All papers authored by Sebastiaan Engelborghs
Refreshing results…
Betty Tijms,
Johan Gobom,
Charlotte Teunissen,
Valerija Dobricic,
Magda Tsolaki 
,
Frans Verhey,
Julius Popp ,
Pablo Martinez-Lage,
Rik Vandenberghe,
Alberto Lleó,
José Molinuévo,
Sebastiaan Engelborghs ,
Yvonne Freund-Levi ,
Lutz Froelich ,
Lars Bertram
and 8 other authors
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,
Frans Verhey,
Julius Popp ,
Pablo Martinez-Lage,
Rik Vandenberghe,
Alberto Lleó,
José Molinuévo,
Sebastiaan Engelborghs ,
Yvonne Freund-Levi ,
Lutz Froelich ,
Lars Bertram
and 8 other authors
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2019
Eline A. J. Willemse ,
Yannick Vermeiren,
Maria-Salud Garcia-Ayllon,
Claire Bridel,
Peter P. De Deyn,
Sebastiaan Engelborghs ,
Wiesje M. van der Flier,
Erwin E. W. Jansen,
Inmaculada B. Lopez-Font,
Vera Mendes ,
Bruno Manadas,
Naomi de Roeck,
Javier Saez-Valero,
Eduard A. Struys,
Eugeen Vanmechelen
and 2 other authors
,
Yannick Vermeiren,
Maria-Salud Garcia-Ayllon,
Claire Bridel,
Peter P. De Deyn,
Sebastiaan Engelborghs ,
Wiesje M. van der Flier,
Erwin E. W. Jansen,
Inmaculada B. Lopez-Font,
Vera Mendes ,
Bruno Manadas,
Naomi de Roeck,
Javier Saez-Valero,
Eduard A. Struys,
Eugeen Vanmechelen
and 2 other authors
Pre-analytical stability of novel cerebrospinal fluid biomarkers
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2018
Yalda Baradaran-Heravi,
Lubina Dillen,
Hung Phuoc Nguyen,
Sara Van Mossevelde,
Jonathan Baets,
Peter De Jonghe,
Sebastiaan Engelborghs ,
Peter P. De Deyn,
Mathieu Vandenbulcke,
Rik Vandenberghe,
Philip Van Damme,
Patrick Cras,
Eric Salmon,
Matthis Synofzik,
Peter Heutink
and 49 other authors
,
Peter P. De Deyn,
Mathieu Vandenbulcke,
Rik Vandenberghe,
Philip Van Damme,
Patrick Cras,
Eric Salmon,
Matthis Synofzik,
Peter Heutink
and 49 other authors
No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients
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Stéphanie Philtjens,
Sara Van Mossevelde,
Julie van der Zee ,
Eline Wauters ,
Lubina Dillen,
Mathieu Vandenbulcke,
Rik Vandenberghe,
Adrian Ivanoiu,
Anne Sieben,
Christiana Willems,
Luisa Benussi ,
Roberta Ghidoni ,
Giuliano Binetti,
Barbara Borroni,
Alessandro Padovani
and 26 other authors
,
Eline Wauters ,
Lubina Dillen,
Mathieu Vandenbulcke,
Rik Vandenberghe,
Adrian Ivanoiu,
Anne Sieben,
Christiana Willems,
Luisa Benussi ,
Roberta Ghidoni ,
Giuliano Binetti,
Barbara Borroni,
Alessandro Padovani
and 26 other authors
Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia
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