Lrrk2 pathogenic substitutions in Parkinson's disease Ignacio F. MataJennifer M. KachergusMatthew J. Farrer Original Article 20 September 2005 Pages: 171 - 177
Differential expression of splice variant and wild-type parkin in sporadic Parkinson's disease E. K. TanH. ShenY. Zhao Original Article 06 August 2005 Pages: 179 - 184
Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC) Maria T. BassiUmberto BalottinMaurizio Taglialatela Original Article 19 October 2005 Pages: 185 - 193
Homozygosity for the p.K136E mutation in the SLC17A5 gene as cause of an Italian severe Salla disease R. BiancheriA. RossiM. Filocamo Original Article 17 September 2005 Pages: 195 - 199
A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effect P. RumpH. H. LemminkA. J. van Essen Original Article 21 October 2005 Pages: 201 - 207
Nonsense mutation in TITF1 in a Portuguese family with benign hereditary chorea Maria do Carmo CostaCristina CostaPatrícia Maciel Original Article 12 October 2005 Pages: 209 - 215
Familial risks for migraine and other headaches among siblings based on hospitalizations in Sweden Kari HemminkiXinjun LiJan Sundquist Original Article 19 October 2005 Pages: 217 - 224
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 Janardan P. PandeyMichiaki KogaNobuhiro Yuki Original Article 29 October 2005 Pages: 225 - 228
Association of sporadic Creutzfeldt–Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean population Byung-Hoon JeongKyung-Hee LeeYong-Sun Kim Short Communication 11 October 2005 Pages: 229 - 232