| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Altered neurodevelopment associated with mutations of RSK2: a morphometric MRI study of Coffin–Lowry syndrome
|
Kesler, Shelli R.
|
|
2007
|
8 |
2 |
p. 143-147
|
artikel
|
| 2 |
A novel gene derived from a segmental duplication shows perturbed expression in Alzheimer’s disease
|
Avramopoulos, Dimitrios
|
|
2007
|
8 |
2 |
p. 111-120
|
artikel
|
| 3 |
Biological effects of the PINK1 c.1366C<T mutation: implications in Parkinson disease pathogenesis
|
Grünewald, Anne
|
|
2007
|
8 |
2 |
p. 103-109
|
artikel
|
| 4 |
Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia
|
Chen, Haijun
|
|
2006
|
8 |
2 |
p. 131-135
|
artikel
|
| 5 |
Large germline deletions and duplication in isolated cerebral cavernous malformation patients
|
Felbor, U.
|
|
2007
|
8 |
2 |
p. 149-153
|
artikel
|
| 6 |
Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson’s disease
|
Taylor, Julie P.
|
|
2007
|
8 |
2 |
p. 95-102
|
artikel
|
| 7 |
Mutations of the LMNA gene can mimic autosomal dominant proximal spinal muscular atrophy
|
Rudnik-Schöneborn, Sabine
|
|
2006
|
8 |
2 |
p. 137-142
|
artikel
|
| 8 |
Nf1 expression is dependent on strain background: implications for tumor suppressor haploinsufficiency studies
|
Hawes, Jessica J.
|
|
2007
|
8 |
2 |
p. 121-130
|
artikel
|
| 9 |
NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe
|
Klebe, Stephan
|
|
2007
|
8 |
2 |
p. 155-157
|
artikel
|
| 10 |
The medial and lateral substantia nigra in Parkinson’s disease: mRNA profiles associated with higher brain tissue vulnerability
|
Duke, D. C.
|
|
2007
|
8 |
2 |
p. 83-94
|
artikel
|
| 11 |
Whole genome expression analyses of single- and double-knock-out mice implicate partially overlapping functions of alpha- and gamma-synuclein
|
Kuhn, Melanie
|
|
2007
|
8 |
2 |
p. 71-81
|
artikel
|
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