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Sara Van Mossevelde

Showing results (21-30 of 28) with videos related to

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Brain : a Journal of Neurology|December 18, 2015
Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohortSara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, et al.
Acta Neuropathologica Communications|November 12, 2015
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brainsJonathan Janssens, Stéphanie Philtjens, Gernot Kleinberger, et al.
JAMA Neurology|February 14, 2017
Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat ExpansionSara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, et al.
Neurobiology of Aging|April 14, 2018
Clinical variability and onset age modifiers in an extended Belgian GRN founder familyEline Wauters, Sara Van Mossevelde, Kristel Sleegers, et al.
Acta Neuropathologica|March 16, 2019
Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitabilityRita Cacace, Bavo Heeman, Sara Van Mossevelde, et al.
Neurobiology of Aging|March 21, 2018
Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementiaStéphanie Philtjens, Sara Van Mossevelde, Julie van der Zee, et al.
Neurobiology of Aging|June 11, 2018
No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patientsYalda Baradaran-Heravi, Lubina Dillen, Hung Phuoc Nguyen, et al.
Human Mutation|December 24, 2016
TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral SclerosisJulie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Brain : a Journal of Neurology|December 18, 2015
Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohortSara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, et al.
Acta Neuropathologica Communications|November 12, 2015
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brainsJonathan Janssens, Stéphanie Philtjens, Gernot Kleinberger, et al.
JAMA Neurology|February 14, 2017
Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat ExpansionSara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, et al.
Neurobiology of Aging|April 14, 2018
Clinical variability and onset age modifiers in an extended Belgian GRN founder familyEline Wauters, Sara Van Mossevelde, Kristel Sleegers, et al.
Acta Neuropathologica|March 16, 2019
Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitabilityRita Cacace, Bavo Heeman, Sara Van Mossevelde, et al.
Neurobiology of Aging|March 21, 2018
Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementiaStéphanie Philtjens, Sara Van Mossevelde, Julie van der Zee, et al.
Neurobiology of Aging|June 11, 2018
No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patientsYalda Baradaran-Heravi, Lubina Dillen, Hung Phuoc Nguyen, et al.
Human Mutation|December 24, 2016
TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral SclerosisJulie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, et al.
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