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Smolders, Stefanie
41
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Online (41)
Mediatypes
Articles (Online) (13)
OpenAccess-fulltext (28)
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1
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/..
?
2
Reply: ATP10B variants in Parkinson's disease—a large cohor..:
Smolders, Stefanie
;
Van Broeckhoven, Christine
Acta Neuropathologica. 141 (2021) 5 - p. 807-808 , 2021
Link:
https://doi.org/10.1007/..
?
3
Reply: ATP10B and the risk for Parkinson's disease:
Smolders, Stefanie
;
Van Broeckhoven, Christine
Acta Neuropathologica. 140 (2020) 3 - p. 403-404 , 2020
Link:
https://doi.org/10.1007/..
?
4
Reply: Segregation of ATP10B variants in families with auto..:
Smolders, Stefanie
;
Van Broeckhoven, Christine
Acta Neuropathologica. 140 (2020) 5 - p. 787-789 , 2020
Link:
https://doi.org/10.1007/..
?
5
Mutated ATP10B increases Parkinson's disease risk by compro..:
The BELNEU consortium
;
Martin, Shaun
;
Smolders, Stefanie
...
Acta Neuropathologica. 139 (2020) 6 - p. 1001-1024 , 2020
Link:
https://doi.org/10.1007/..
?
6
Genetic perspective on the synergistic connection between v..:
Smolders, Stefanie
;
Van Broeckhoven, Christine
Acta Neuropathologica Communications. 8 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1186/..
?
7
Global investigation and meta-analysis of theC9orf72(G4C2)n..:
Theuns, Jessie
;
Verstraeten, Aline
;
Sleegers, Kristel
...
Neurology. 83 (2014) 21 - p. 1906-1913 , 2014
Link:
https://doi.org/10.1212/..
?
8
Contribution of rare homozygous and compound heterozygous V..:
Smolders, Stefanie
;
Philtjens, Stéphanie
;
Crosiers, David
...
https://edepot.wur.nl/541545. , 2021
Link:
https://research.wur.nl/..
?
9
Reply: ATP10B variants in Parkinson's disease—a large cohor..:
Smolders, Stefanie
;
Van Broeckhoven, Christine
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8043888/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
10
Contribution of rare homozygous and compound heterozygous V..:
Smolders, Stefanie
;
Philtjens, Stéphanie
;
Crosiers, David
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881566/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
11
Mutated ATP10B increases Parkinson's disease risk by compro..:
Martin, Shaun
;
Smolders, Stefanie
;
Van den Haute, Chris
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7244618/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
12
Global investigation and meta-analysis of the C9orf72 (G4C2..:
Theuns, Jessie
;
Verstraeten, Aline
;
Sleegers, Kristel
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC. , 2014
Link:
http://www.ncbi.nlm.nih...
?
13
Contribution of rare homozygous and compound heterozygous V..:
Stefanie Smolders
;
Stéphanie Philtjens
;
David Crosiers
...
https://doi.org/10.1186/s40478-021-01121-w. , 2021
Link:
https://doi.org/10.1186/..
?
14
Genetic perspective on the synergistic connection between v..:
Stefanie Smolders
;
Christine Van Broeckhoven
http://link.springer.com/article/10.1186/s40478-020-00935-4. , 2020
Link:
https://doi.org/10.1186/..
?
15
Additional file 1 of Contribution of rare homozygous and co..:
Stefanie Smolders (10138207)
;
Stéphanie Philtjens (3523664)
;
David Crosiers (10138210)
...
https://figshare.com/articles/journal_contribution/Additional_file_1_of_Contribution_of_rare_homozygous_and_compound_heterozygous_VPS13C_missense_mutations_to_dementia_with_Lewy_bodies_and_Parkinson_s_disease/13978780. , 2021
Link:
https://doi.org/10.6084/..
1-15