Whole genome expression analyses of single- and double-knock-out mice implicate partially overlapping functions of alpha- and gamma-synuclein Melanie KuhnKarina HaebigOlaf Riess Original Article 22 February 2007 Pages: 71 - 81
The medial and lateral substantia nigra in Parkinson’s disease: mRNA profiles associated with higher brain tissue vulnerability D. C. DukeL. B. MoranM. B. Graeber Original Article 09 January 2007 Pages: 83 - 94
Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson’s disease Julie P. TaylorMary M. HulihanMatthew J. Farrer Original Article 16 January 2007 Pages: 95 - 102
Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesis Anne GrünewaldGuido J. BreedveldVincenzo Bonifati Original Article 12 January 2007 Pages: 103 - 109
A novel gene derived from a segmental duplication shows perturbed expression in Alzheimer’s disease Dimitrios AvramopoulosRuihua WangSusan S. Bassett Original Article 16 February 2007 Pages: 111 - 120
Nf1 expression is dependent on strain background: implications for tumor suppressor haploinsufficiency studies Jessica J. HawesRobert G. TuskanKarlyne M. Reilly Original Article 11 January 2007 Pages: 121 - 130
Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia Haijun ChenChristian von HehnFuki M. Hisama Original Article Open access 29 November 2006 Pages: 131 - 135
Mutations of the LMNA gene can mimic autosomal dominant proximal spinal muscular atrophy Sabine Rudnik-SchönebornElke BotzenhartKlaus Zerres Original Article 29 November 2006 Pages: 137 - 142
Altered neurodevelopment associated with mutations of RSK2: a morphometric MRI study of Coffin–Lowry syndrome Shelli R. KeslerRichard J. SimensenAllan L. Reiss Short Communication 22 February 2007 Pages: 143 - 147
Large germline deletions and duplication in isolated cerebral cavernous malformation patients U. FelborS. GaetznerA. M. Siegel Short Communication 09 January 2007 Pages: 149 - 153
NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe Stephan KlebeArnaud LacourGiovanni Stevanin Letters to the Editors 05 January 2007 Pages: 155 - 157