|
🐜
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Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
19 auth.
Elise Cuyvers,
K. Bettens,
Stéphanie Philtjens,
T. Langenhove,
I. Gijselinck,
J. Zee,
S. Engelborghs,
M. Vandenbulcke,
Jasper Van Dongen,
N. Geerts,
...
Githa Maes,
Maria Mattheijssens,
K. Peeters,
P. Cras,
R. Vandenberghe,
P. Deyn,
C. Broeckhoven,
M. Cruts,
K. Sleegers
|
7 |
2014 |
7
🐜
|
|
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Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability
29 auth.
Rita Cacace,
Bavo Heeman,
Sara Van Mossevelde,
Arne De Roeck,
Julie Hoogmartens,
Peter De Rijk,
Helena Gossye,
Kristof De Vos,
Wouter De Coster,
Mojca Strazisar,
Greet De Baets,
J. Schymkowitz,
F. Rousseau,
N. Geerts,
Tim De Pooter,
...
K. Peeters,
A. Sieben,
Jean-Jacques Martin,
S. Engelborghs,
E. Salmon,
P. Santens,
R. Vandenberghe,
P. Cras,
Peter P De Deyn,
John C van Swieten,
Cornelia M van Duijn,
J. van der Zee,
K. Sleegers,
C. van Broeckhoven
|
5 |
2019 |
5
🐜
|
|
🐜
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Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study
43 auth.
Elise Cuyvers,
J. Zee,
K. Bettens,
S. Engelborghs,
M. Vandenbulcke,
C. Robberecht,
L. Dillen,
C. Merlin,
N. Geerts,
C. Graff,
H. Thonberg,
H. Chiang,
P. Pastor,
S. Ortega-Cubero,
M. Pastor,
...
J. Diehl-Schmid,
P. Alexopoulos,
L. Benussi,
R. Ghidoni,
G. Binetti,
B. Nacmias,
S. Sorbi,
Raquel Sánchez-Valle,
A. Lladó,
E. Gelpí,
M. R. Almeida,
I. Santana,
J. Clarimón,
A. Lleó,
J. Fortea,
A. Mendonça,
Madalena Martins,
B. Borroni,
A. Padovani,
R. Matěj,
Z. Rohan,
A. Ruiz,
G. Frisoni,
G. Fabrizi,
R. Vandenberghe,
P. Deyn,
C. Broeckhoven,
K. Sleegers
|
5 |
2015 |
5
🐜
|
|
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Rare Variants in PLD3 Do Not Affect Risk for Early‐Onset Alzheimer Disease in a European Consortium Cohort
42 auth.
Rita Cacace,
T. Van den Bossche,
S. Engelborghs,
N. Geerts,
A. Laureys,
L. Dillen,
C. Graff,
H. Thonberg,
H. Chiang,
P. Pastor,
S. Ortega-Cubero,
M. Pastor,
J. Diehl-Schmid,
P. Alexopoulos,
L. Benussi,
...
R. Ghidoni,
G. Binetti,
B. Nacmias,
S. Sorbi,
Raquel Sánchez-Valle,
A. Lladó,
E. Gelpí,
M. R. Almeida,
I. Santana,
M. Tsolaki,
M. Koutroumani,
J. Clarimón,
A. Lleó,
J. Fortea,
A. de Mendonça,
Madalena Martins,
B. Borroni,
A. Padovani,
R. Matěj,
Z. Rohan,
M. Vandenbulcke,
R. Vandenberghe,
P. D. de Deyn,
P. Cras,
J. van der Zee,
K. Sleegers,
C. van Broeckhoven
|
4 |
2015 |
4
🐜
|
|
🐜
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Loss of function mutations in dipeptidyl peptidase 6 in Alzheimer disease and Frontotemporal dementia: a novel pathway in neurodegeneration
24 auth.
Rita Cacace,
T. V. D. Bossche,
J. Lippiat,
J. Janssens,
G. Baets,
S. Engelborghs,
A. Sieben,
M. Vandenbulcke,
P. Rijk,
Elise Cuyvers,
...
C. V. Cauwenberghe,
C. Robberecht,
L. Dillen,
C. Merlin,
N. Geerts,
R. Vandenberghe,
J. Martin,
P. Deyn,
J. Schymkowitz,
Stuart Maudsley,
M. Cruts,
J. Zee,
K. Sleegers,
C. Broeckhoven
|
0 |
2016 |
0
🐜
|
|
🐜
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Evolution of cerebral PET glucose metabolism from presymptomatic to symtomatic frontotemporal dementia linked to chromosome 3 (FTD-3) - a voxel based SPM analysis
35 auth.
Rita Cacace,
P. Rijk,
J. Zee,
T. V. D. Bossche,
G. Waldemar,
J. Lippiat,
J. Janssens,
P. Johannsen,
G. Baets,
S. Engelborghs,
I. Law,
A. Sieben,
M. Vandenbulcke,
Nina Rostgaard,
Elise Cuyvers,
...
P. Roos,
C. V. Cauwenberghe,
C. Robberecht,
L. Dillen,
C. Hansen,
C. Merlin,
N. Geerts,
J. Stokholm,
R. Vandenberghe,
J. Martin,
Julia Brown,
P. Deyn,
J. Schymkowitz,
A. Isaacs,
Stuart Maudsley,
M. Cruts,
T. Nielsen,
K. Sleegers,
J. Nielsen,
C. Broeckhoven
|
0 |
2016 |
0
🐜
|
|
🐜
|
Compensatory mechanisms enables intelligibility in prodromal Parkinson's disease
7 auth.
T. Thies,
D. Muecke,
N. Geerts,
A. Seger,
G. Fink,
M. Barbe,
...
M. Sommerauer
|
0 |
2022 |
0
🐜
|
|
🐜
|
EXPLORING THE MOLECULAR MECHANISM OF NEURONAL HYPEREXCITABILITY IN DEMENTIA
11 auth.
Rita Cacace,
Julie Hoogmartens,
S. V. Mossevelde,
T. V. D. Bossche,
N. Geerts,
R. Vandenberghe,
...
P. Deyn,
J. Zee,
S. Engelborghs,
K. Sleegers,
C. Broeckhoven
|
0 |
2018 |
0
🐜
|
