Digitale Bibliotheek
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                             13 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Accumulation of dysfunctional SOD1 protein in Parkinson’s disease is not associated with mutations in the SOD1 gene Trist, Benjamin G.
2017
135 1 p. 155-156
artikel
2 A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8 Bouhy, Delphine
2017
135 1 p. 131-148
artikel
3 CASQ1 mutations impair calsequestrin polymerization and cause tubular aggregate myopathy Böhm, Johann
2017
135 1 p. 149-151
artikel
4 Comprehensive molecular characterisation of epilepsy-associated glioneuronal tumours Stone, Thomas J.
2017
135 1 p. 115-129
artikel
5 Does Parkinson’s disease start in the gut? Lionnet, Arthur
2017
135 1 p. 1-12
artikel
6 MSA prions exhibit remarkable stability and resistance to inactivation Woerman, Amanda L.
2017
135 1 p. 49-63
artikel
7 Multiple system atrophy: experimental models and reality Overk, Cassia
2017
135 1 p. 33-47
artikel
8 Parkinson’s disease: experimental models and reality Jiang, Peizhou
2017
135 1 p. 13-32
artikel
9 Phenotyping cognitive impairment in dialysis patients: insights from experimental mouse models Kelly, Dearbhla M.
2017
135 1 p. 157-158
artikel
10 Polygenic hazard score: an enrichment marker for Alzheimer’s associated amyloid and tau deposition Tan, Chin Hong
2017
135 1 p. 85-93
artikel
11 Regional levels of physiological α-synuclein are directly associated with Lewy body pathology Erskine, Daniel
2017
135 1 p. 153-154
artikel
12 Spread of aggregates after olfactory bulb injection of α-synuclein fibrils is associated with early neuronal loss and is reduced long term Rey, Nolwen L.
2017
135 1 p. 65-83
artikel
13 Uncoupling N-acetylaspartate from brain pathology: implications for Canavan disease gene therapy von Jonquieres, Georg
2017
135 1 p. 95-113
artikel
                             13 gevonden resultaten
 
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