Ghent University Academic Bibliography

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Digitalized transcranial electrical stimulation : a consensus statement

Andre R. Brunoni, Hamed Ekhtiari, Andrea Antal, Paradee Auvichayapat, Chris Baeken (UGent) , Isabela M. Benseñor, Marom Bikson, Paulo Boggio, Barbara Borroni, Filippo Brighina, et al.

(2022) CLINICAL NEUROPHYSIOLOGY. 143. p.154-165
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Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort

Jan Verheijen, Julie van der Zee, Ilse Gijselinck, Tobi Van den Bossche, Lubina Dillen, Bavo Heeman, Estrella Gómez-Tortosa, Albert Lladó, Raquel Sanchez-Valle, Caroline Graff, et al.

(2018) NEUROBIOLOGY OF AGING. 62. p.245.e1-245.e7
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No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

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, et al.

(2018) NEUROBIOLOGY OF AGING. 69.
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TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis

Julie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, Federica Perrone, Lubina Dillen, Bavo Heeman, Veerle Bäumer, Sebastiaan Engelborghs, Jan De Bleecker (UGent) , Jonathan Baets, et al.

(2017) HUMAN MUTATION. 38(3). p.297-309
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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Julie van der Zee, Tim Van Langenhove (UGent) , Gabor G Kovacs, Lubina Dillen, William Deschamps, Sebastiaan Engelborghs, Radoslav Matěj, Mathieu Vandenbulcke, Anne Sieben (UGent) , Bart Dermaut (UGent) , et al.

(2014) ACTA NEUROPATHOLOGICA. 128(3). p.397-410
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A pan-European study of the C9orf72 repeat associated with FTLD : geographic prevalence, genomic instability, and intermediate repeats

Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove (UGent) , Jessie Theuns, Sebastiaan Engelborghs, Stéphanie Philtjens, Mathieu Vandenbulcke, Kristel Sleegers, Anne Sieben (UGent) , et al.

(2013) HUMAN MUTATION. 34(2). p.363-373

Academic Bibliography

Digitalized transcranial electrical stimulation : a consensus statement

Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort

No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

A pan-European study of the C9orf72 repeat associated with FTLD : geographic prevalence, genomic instability, and intermediate repeats

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