| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model
|
Deng, Ruizhi
|
|
|
146 |
2 |
p. 353-368
|
artikel
|
| 2 |
A T-cell antigen atlas for meningioma: novel options for immunotherapy
|
Medici, Gioele
|
|
|
146 |
2 |
p. 173-190
|
artikel
|
| 3 |
Central and peripheral myeloid-derived suppressor cell-like cells are closely related to the clinical severity of multiple sclerosis
|
Ortega, María Cristina
|
|
|
146 |
2 |
p. 263-282
|
artikel
|
| 4 |
Defective cerebellar ryanodine receptor type 1 and endoplasmic reticulum calcium ‘leak’ in tremor pathophysiology
|
Martuscello, Regina T.
|
|
|
146 |
2 |
p. 301-318
|
artikel
|
| 5 |
From methylation to myelination: epigenomic and transcriptomic profiling of chronic inactive demyelinated multiple sclerosis lesions
|
Tiane, Assia
|
|
|
146 |
2 |
p. 283-299
|
artikel
|
| 6 |
Individual myasthenia gravis autoantibody clones can efficiently mediate multiple mechanisms of pathology
|
Pham, Minh C.
|
|
|
146 |
2 |
p. 319-336
|
artikel
|
| 7 |
Mutant LRRK2 exacerbates immune response and neurodegeneration in a chronic model of experimental colitis
|
Cabezudo, Diego
|
|
|
146 |
2 |
p. 245-261
|
artikel
|
| 8 |
Mutation ∆K281 in MAPT causes Pick’s disease
|
Schweighauser, Manuel
|
|
|
146 |
2 |
p. 211-226
|
artikel
|
| 9 |
SCA34 caused by ELOVL4 L168F mutation is a lysosomal lipid storage disease sharing pathology features with neuronal ceroid lipofuscinosis and peroxisomal disorders
|
Ellezam, Benjamin
|
|
|
146 |
2 |
p. 337-352
|
artikel
|
| 10 |
Tau seeding and spreading in vivo is supported by both AD-derived fibrillar and oligomeric tau
|
Mate De Gerando, Anastasie
|
|
|
146 |
2 |
p. 191-210
|
artikel
|
| 11 |
Transcriptomic profiling of Parkinson's disease brains reveals disease stage specific gene expression changes
|
Cappelletti, Chiara
|
|
|
146 |
2 |
p. 227-244
|
artikel
|
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