| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Alpha-synuclein suppresses mitochondrial protease ClpP to trigger mitochondrial oxidative damage and neurotoxicity
|
Hu, Di
|
|
2019
|
137 |
6 |
p. 939-960
|
artikel
|
| 2 |
Caspase-4 mediates cytoplasmic accumulation of TDP-43 in the primate brains
|
Yin, Peng
|
|
2019
|
137 |
6 |
p. 919-937
|
artikel
|
| 3 |
Correction to: H3.3 K27M depletion increases differentiation and extends latency of diffuse intrinsic pontine glioma growth in vivo
|
Silveira, André B.
|
|
2019
|
137 |
6 |
p. 1021
|
artikel
|
| 4 |
Demonstration of prion-like properties of mutant huntingtin fibrils in both in vitro and in vivo paradigms
|
Masnata, Maria
|
|
2019
|
137 |
6 |
p. 981-1001
|
artikel
|
| 5 |
Desmoplastic/nodular medulloblastomas (DNMB) and medulloblastomas with extensive nodularity (MBEN) disclose similar epigenetic signatures but different transcriptional profiles
|
Korshunov, Andrey
|
|
2019
|
137 |
6 |
p. 1003-1015
|
artikel
|
| 6 |
Disrupted neuronal trafficking in amyotrophic lateral sclerosis
|
Burk, Katja
|
|
2019
|
137 |
6 |
p. 859-877
|
artikel
|
| 7 |
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD
|
Pottier, Cyril
|
|
2019
|
137 |
6 |
p. 879-899
|
artikel
|
| 8 |
Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability
|
Cacace, Rita
|
|
2019
|
137 |
6 |
p. 901-918
|
artikel
|
| 9 |
LRRK2 modifies α-syn pathology and spread in mouse models and human neurons
|
Bieri, Gregor
|
|
2019
|
137 |
6 |
p. 961-980
|
artikel
|
| 10 |
Severe bornavirus-encephalitis presenting as Guillain–Barré-syndrome
|
Coras, Roland
|
|
2019
|
137 |
6 |
p. 1017-1019
|
artikel
|
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