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Breedveld, Guido J.
166
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Online (166)
Mediatypes
Articles (Online) (84)
OpenAccess-fulltext (82)
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1
LRP10 and α-synuclein transmission in Lewy body diseases:
Carreras Mascaro, Ana
;
Grochowska, Martyna M.
;
Boumeester, Valerie
...
Cellular and Molecular Life Sciences. 81 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1007/..
?
2
Clinical, neuroimaging and genetic findings in Brazilian pa..:
Araújo Salomão, Rubens Paulo
;
Rezende Filho, Flávio Moura
;
Borges, Vanderci
...
Parkinsonism & Related Disorders. 123 (2024) - p. 106103 , 2024
Link:
https://doi.org/10.1016/..
?
3
deCLUTTER2+ – a pipeline to analyze calcium traces in a ste..:
Grochowska, Martyna M.
;
Ferraro, Federico
;
Mascaro, Ana Carreras
...
Disease Models & Mechanisms. 16 (2023) 6 - p. , 2023
Link:
https://doi.org/10.1242/..
?
4
Isolated Paroxysmal Non‐kinesigenic Dystonia Associated wit..:
Agarwal, Pankaj A.
;
Kuipers, Demy J.S.
;
Fevga, Christina
...
Movement Disorders. 37 (2022) 10 - p. 2166-2167 , 2022
Link:
https://doi.org/10.1002/..
?
5
AOPEP Homozygous Loss‐of‐Function Variant in an Indian Pati..:
Fevga, Christina
;
Ferraro, Federico
;
Breedveld, Guido J.
..
Movement Disorders. 37 (2022) 4 - p. 874-875 , 2022
Link:
https://doi.org/10.1002/..
?
6
Segmental dystonia as the prominent phenotype resulting fro..:
Fevga, Christina
;
Ferraro, Federico
;
Breedveld, Guido J.
..
Parkinsonism & Related Disorders. 103 (2022) - p. 141-143 , 2022
Link:
https://doi.org/10.1016/..
?
7
A multiplex pedigree with pathologically confirmed multiple..:
Fanciulli, Alessandra
;
Leys, Fabian
;
Lehner, Fabienne
...
Brain Communications. 4 (2022) 4 - p. , 2022
Link:
https://doi.org/10.1093/..
?
8
A new alpha-synuclein missense variant (Thr72Met) in two Tu..:
Fevga, Christina
;
Park, Yangshin
;
Lohmann, Ebba
...
Parkinsonism & Related Disorders. 89 (2021) - p. 63-72 , 2021
Link:
https://doi.org/10.1016/..
?
9
LRP10 interacts with SORL1 in the intracellular vesicle tra..:
Grochowska, Martyna M.
;
Carreras Mascaro, Ana
;
Boumeester, Valerie
...
Acta Neuropathologica. 142 (2021) 1 - p. 117-137 , 2021
Link:
https://doi.org/10.1007/..
?
10
EIF2AK2 Missense Variants Associated with Early Onset Gener..:
Kuipers, Demy J. S.
;
Mandemakers, Wim
;
Lu, Chin‐Song
...
Annals of Neurology. 89 (2020) 3 - p. 485-497 , 2020
Link:
https://doi.org/10.1002/..
?
11
LRP10 variants in progressive supranuclear palsy:
Vergouw, Leonie J.M.
;
Melhem, Shamiram
;
Donker Kaat, Laura
...
Neurobiology of Aging. 94 (2020) - p. 311.e5-311.e10 , 2020
Link:
https://doi.org/10.1016/..
?
12
Clinical and Pathological Phenotypes of LRP10 Variant Carri..:
Vergouw, Leonie J. M.
;
Geut, Hanneke
;
Breedveld, Guido
...
Journal of Alzheimer's Disease. 76 (2020) 3 - p. 1161-1170 , 2020
Link:
https://doi.org/10.3233/..
?
13
Primary familial brain calcification caused by MYORG mutati..:
Taglia, Ilaria
;
Kuipers, Demy J.S.
;
Breedveld, Guido J.
...
Parkinsonism & Related Disorders. 67 (2019) - p. 24-26 , 2019
Link:
https://doi.org/10.1016/..
?
14
Late-onset phenotype associated with a homozygous GJC2 miss..:
Kuipers, Demy J.S.
;
Tufekcioglu, Zeynep
;
Bilgiç, Başar
...
Parkinsonism & Related Disorders. 66 (2019) - p. 228-231 , 2019
Link:
https://doi.org/10.1016/..
?
15
Low prevalence of known pathogenic mutations in dominant PD..:
Puschmann, Andreas
;
Jiménez-Ferrer, Itzia
;
Lundblad-Andersson, Elin
...
Parkinsonism & Related Disorders. 66 (2019) - p. 158-165 , 2019
Link:
https://doi.org/10.1016/..
1-15