| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Brain-derived neurotrophic factor: its impact upon neuroplasticity and neuroplasticity inducing transcranial brain stimulation protocols
|
Chaieb, L.
|
|
2014
|
15 |
1 |
p. 1-11
|
artikel
|
| 2 |
'Comment on the Paper "SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystonia" by Baker et al.'
|
Oliveira, João
|
|
2013
|
15 |
1 |
p. 79
|
artikel
|
| 3 |
Evidence of a role for SNCA in impulse control in humans
|
Guillot, Casey R.
|
|
2013
|
15 |
1 |
p. 77-78
|
artikel
|
| 4 |
Expanding the spectrum of megalencephalic leukoencephalopathy with subcortical cysts in two patients with GLIALCAM mutations
|
Arnedo, Tanit
|
|
2013
|
15 |
1 |
p. 41-48
|
artikel
|
| 5 |
Founder effect and ancestral origin of the spinocerebellar ataxia type 7 (SCA7) mutation in Mexican families
|
García-Velázquez, Lizbeth E.
|
|
2013
|
15 |
1 |
p. 13-17
|
artikel
|
| 6 |
Genetic determinants of neuroglobin transcription
|
Wang, R.
|
|
2013
|
15 |
1 |
p. 65-75
|
artikel
|
| 7 |
Mutations in MAPT give rise to aneuploidy in animal models of tauopathy
|
Rossi, Giacomina
|
|
2013
|
15 |
1 |
p. 31-40
|
artikel
|
| 8 |
Rare variants in LRRK1 and Parkinson's disease
|
Schulte, Eva C.
|
|
2013
|
15 |
1 |
p. 49-57
|
artikel
|
| 9 |
Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizures
|
McFarland, Karen N.
|
|
2013
|
15 |
1 |
p. 59-64
|
artikel
|
| 10 |
SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystonia
|
Baker, Matt
|
|
2013
|
15 |
1 |
p. 23-30
|
artikel
|
| 11 |
The documentation of consent and disclosure of neurogenetic testing outside clinical genetics
|
Lo, C.
|
|
2014
|
15 |
1 |
p. 19-21
|
artikel
|
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