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Van Mossevelde, Sara
86
results:
Search for persons
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Format
Online (86)
Mediatypes
Articles (Online) (50)
OpenAccess-fulltext (36)
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1
Tacrolimus-induced cognitive impairment: a case report:
Deprez, Valerie
;
Goeman, Johan
;
Van Mossevelde, Sara
Acta Neurologica Belgica. , 2024
Link:
https://doi.org/10.1007/..
?
2
Patients carrying the mutation p.R406W in MAPT present with..:
Gossye, Helena
;
Van Mossevelde, Sara
;
Sieben, Anne
...
Brain. 146 (2022) 4 - p. 1624-1636 , 2022
Link:
https://doi.org/10.1093/..
?
3
Frequent MAPT p.R406W Carriers with a Nonconforming FTD Phe..:
Gossye, Helena
;
Van Mossevelde, Sara
;
Van Der Zee, Julie
...
Neurology. 98 (2022) 18_supplement - p. , 2022
Link:
https://doi.org/10.1212/..
?
4
Prevalence and Phenotype of TBK1 Mutations: an In-Depth Des..:
Gossye, Helena
;
Van Mossevelde, Sara
;
De Bleecker, Jan
...
Neurology. 98 (2022) 18_supplement - p. , 2022
Link:
https://doi.org/10.1212/..
?
5
Microtubule associated protein tau p.R406W patient carriers..:
Gossye, Helena
;
Van Mossevelde, Sara
;
Sieben, Anne
...
Alzheimer's & Dementia. 18 (2022) S3 - p. , 2022
Link:
https://doi.org/10.1002/..
?
6
Extensive genetic and phenotypic description ofMAPTp.R406W ..:
Gossye, Helena
;
Van Mossevelde, Sara
;
van der Zee, Julie
...
Alzheimer's & Dementia. 17 (2021) S3 - p. , 2021
Link:
https://doi.org/10.1002/..
?
7
No association of CpG SNP rs9357140 with onset age in Belgi..:
Koçoğlu, Cemile
;
Gossye, Helena
;
Dillen, Lubina
...
Neurobiology of Aging. 97 (2021) - p. 145.e1-145.e4 , 2021
Link:
https://doi.org/10.1016/..
?
8
Contribution of rare homozygous and compound heterozygous V..:
BELNEU consortium
;
Smolders, Stefanie
;
Philtjens, Stéphanie
...
Acta Neuropathologica Communications. 9 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
?
9
In-Depth Phenotypic Description Of Pathogenic TBK1 Mutation..:
Gossye, Helena
;
Van Mossevelde, Sara
;
Van Der Zee, Julie
...
Neurology. 96 (2021) 15_supplement - p. , 2021
Link:
https://doi.org/10.1212/..
?
10
In‐depth phenotypic description of pathogenicTBK1mutations:..:
Gossye, Helena
;
Van Mossevelde, Sara
;
van der Zee, Julie
...
Alzheimer's & Dementia. 17 (2021) S3 - p. , 2021
Link:
https://doi.org/10.1002/..
?
11
Extensive Genetic And Phenotypic Description Of MAPT p.R406..:
Gossye, Helena
;
Van Mossevelde, Sara
;
Van Der Zee, Julie
...
Neurology. 96 (2021) 15_supplement - p. , 2021
Link:
https://doi.org/10.1212/..
?
12
Highly Frequent MAPT p.R406W Carriers with a Nonconforming ..:
Gossye, Helena
;
Van Mossevelde, Sara
;
Van Der Zee, Julie
...
Neurology. 94 (2020) 15_supplement - p. , 2020
Link:
https://doi.org/10.1212/..
?
13
Loss of DPP6 in neurodegenerative dementia: a genetic playe..:
the BELNEU Consortium
;
Cacace, Rita
;
Heeman, Bavo
...
Acta Neuropathologica. 137 (2019) 6 - p. 901-918 , 2019
Link:
https://doi.org/10.1007/..
?
14
P1‐210: INVESTIGATING THE INVOLVEMENT OF THE DPP6‐KV4.2 PRO..:
Cacace, Rita
;
De Vos, Kristof
;
Heeman, Bavo
...
Alzheimer's & Dementia. 15 (2019) 7S_Part_6 - p. , 2019
Link:
https://doi.org/10.1016/..
?
15
Association of short-term cognitive decline and MCI-to-AD d..:
Ottoy, Julie
;
Niemantsverdriet, Ellis
;
Verhaeghe, Jeroen
...
NeuroImage: Clinical. 22 (2019) - p. 101771 , 2019
Link:
https://doi.org/10.1016/..
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