no |
title |
author |
magazine |
year |
volume |
issue |
page(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 |
article |
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 |
article |
3 |
Differential expression of splice variant and wild-type parkin in sporadic Parkinson's disease
|
Tan, E. K. |
|
2005 |
6 |
4 |
p. 179-184 |
article |
4 |
Familial risks for migraine and other headaches among siblings based on hospitalizations in Sweden
|
Hemminki, Kari |
|
2005 |
6 |
4 |
p. 217-224 |
article |
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 |
article |
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 |
article |
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 |
article |
8 |
Lrrk2 pathogenic substitutions in Parkinson's disease
|
Mata, Ignacio F. |
|
2005 |
6 |
4 |
p. 171-177 |
article |
9 |
Nonsense mutation in TITF1 in a Portuguese family with benign hereditary chorea
|
Carmo Costa, Maria do |
|
2005 |
6 |
4 |
p. 209-215 |
article |