Researcher
Christine Van Broeckhoven
- Keywords:Medicine
- Disciplines:Translational sciences, Clinical sciences, Basic sciences
Affiliations
- Pathologic Biochemistry and Physiology (Department)
Member
From1 Oct 1999 → 30 Sep 2003 - Medicine and Pharmacy academic/administration (Office)
Member
From1 Oct 1993 → 30 Sep 1999
Publications
21 - 30 of 78
- MRI predictors of amyloid pathology(2018)
Authors: Mara Ten Kate, Alberto Redolfi, Enrico Peira, Isabelle Bos, Stephanie J Vos, Rik Vandenberghe, Silvy Gabel, Jolien Schaeverbeke, Philip Scheltens, Olivier Blin, et al.
- Genetic screening in early-onset dementia patients with unclear phenotype(2018)
Authors: Federica Perrone, Rita Cacace, Sara Van Mossevelde, Tobi Van den Bossche, Peter De Deyn, Patrick Cras, Sebastiaan Engelborghs, Julie Van Der Zee, Christine Van Broeckhoven
Pages: 292.e7-292.e14 - No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients(2018)
Authors: Yalda Baradaran-Heravi, Lubina Dillen, Hung Phuoc Nguyen, Sara Van Mossevelde, Jonathan Baets, Peter De Jonghe, Sebastiaan Engelborghs, Peter De Deyn, Mathieu Vandenbulcke, Rik Vandenberghe, et al.
Pages: 293.e9-293.e11 - The EMIF-AD Multimodal Biomarker Discovery study(2018)
Authors: Isabelle Bos, Stephanie Vos, Rik Vandenberghe, Philip Scheltens, Sebastiaan Engelborghs, Giovanni Frisoni, José Luis Molinuevo, Anders Wallin, Alberto Lleó, Julius Popp, et al.
- Clinical variability and onset age modifiers in an extended Belgian GRN founder family(2018)
Authors: Eline Wauters, Sara Van Mossevelde, Kristel Sleegers, Julie Van Der Zee, Sebastiaan Engelborghs, Anne Sieben, Rik Vandenberghe, Stéphanie Philtjens, Marleen Van Den Broeck, Karin Peeters, et al.
Pages: 84-94 - Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia(2018)
Authors: Stéphanie Philtjens, Sara Van Mossevelde, Julie Van Der Zee, Eline Wauters, Lubina Dillen, Mathieu Vandenbulcke, Rik Vandenberghe, Adrian Ivanoiu, Anne Sieben, Christiana Willems, et al.
Pages: 181.e3-181.e10 - Genotype-phenotype links in frontotemporal lobar degeneration(2018)
Authors: Sara Van Mossevelde, Julie van der Zee, Christine Van Broeckhoven
Pages: 363-378 - An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease(2018)
Authors: Arne De Roeck, Lena Duchateau, Jasper Van Dongen, Rita Cacace, Maria Bjerke, Tobi Van den Bossche, Patrick Cras, Rik Vandenberghe, Peter De Deyn, Sebastiaan Engelborghs, et al.
Pages: 827-837 - Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degeneration(2018)
Authors: Joery Goossens, Maria Bjerke, Sara Van Mossevelde, Tobi Van den Bossche, Johan Goeman, Bart De Vil, Anne Sieben, Jean-Jacques Martin, Patrick Cras, Peter Paul De Deyn, et al.
- Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion(2018)
Authors: Jelle van den Ameele, Ivana Jedlickova, Anna Pristoupilova, Anne Sieben, Sara Van Mossevelde, Chantal Ceuterick-de Groote, Helena Hůlková, Radoslav Matej, Alfred Meurs, Christine Van Broeckhoven, et al.
Pages: 1-6