| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effect
|
Rump, P.
|
|
2005
|
6 |
4 |
p. 201-207
|
artikel
|
| 2 |
Association of sporadic Creutzfeldt–Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean population
|
Jeong, Byung-Hoon
|
|
2005
|
6 |
4 |
p. 229-232
|
artikel
|
| 3 |
Differential expression of splice variant and wild-type parkin in sporadic Parkinson's disease
|
Tan, E. K.
|
|
2005
|
6 |
4 |
p. 179-184
|
artikel
|
| 4 |
Familial risks for migraine and other headaches among siblings based on hospitalizations in Sweden
|
Hemminki, Kari
|
|
2005
|
6 |
4 |
p. 217-224
|
artikel
|
| 5 |
Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC)
|
Bassi, Maria T.
|
|
2005
|
6 |
4 |
p. 185-193
|
artikel
|
| 6 |
Homozygosity for the p.K136E mutation in the SLC17A5 gene as cause of an Italian severe Salla disease
|
Biancheri, R.
|
|
2005
|
6 |
4 |
p. 195-199
|
artikel
|
| 7 |
Immunoglobulin KM allotypes are associated with the prevalence of autoantibodies to GD1a ganglioside, but not with susceptibility to the disease, in Japanese patients with Guillain–Barré syndrome
|
Pandey, Janardan P.
|
|
2005
|
6 |
4 |
p. 225-228
|
artikel
|
| 8 |
Lrrk2 pathogenic substitutions in Parkinson's disease
|
Mata, Ignacio F.
|
|
2005
|
6 |
4 |
p. 171-177
|
artikel
|
| 9 |
Nonsense mutation in TITF1 in a Portuguese family with benign hereditary chorea
|
Carmo Costa, Maria do
|
|
2005
|
6 |
4 |
p. 209-215
|
artikel
|
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