Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13 David KemlinkGiuseppe PlazziPasquale Montagna Original Article Open access 10 January 2008 Pages: 75 - 82
RNA interference of LRRK2–microarray expression analysis of a Parkinson’s disease key player K. HäbigM. WalterM. Bonin Original Article 21 December 2007 Pages: 83 - 94
Breakpoint characterization of a novel NF1 multiexonic deletion: a case showing expression of the mutated allele Francesca OrzanMichela StroppiPaola Riva Original Article 10 January 2008 Pages: 95 - 100
Structural genomic variation in ischemic stroke Mar MatarinJavier Simon-SanchezAndrew B. Singleton Original Article 21 February 2008 Pages: 101 - 108
Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation Ana B. Rodríguez-MartínezMiguel A. Alfonso-SánchezMarian M. de Pancorbo Original Article 18 March 2008 Pages: 109 - 118
Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population Beyhan TüysüzFatih BayrakliMurat Gunel Original Article 06 March 2008 Pages: 119 - 125
Further examination of the candidate genes in chromosome 12p13 locus for late-onset Alzheimer disease Joseph H. LeeRong ChengRichard Mayeux Original Article 14 March 2008 Pages: 127 - 138
Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families Francesca MadiaPasquale StrianoFederico Zara Short Communication 30 January 2008 Pages: 139 - 142
Is the early-onset torsion dystonia (EOTD) linked to TOR1A gene as frequent as expected in France? M. Y. FrédéricF. ClotG. Collod-Beroud Short Communication 06 March 2008 Pages: 143 - 150
Long-range PCR for the diagnosis of spinocerebellar ataxia type 10 Tatsuaki KurosakiTohru MatsuuraShintaroh Ueda Letter to the Editors 16 January 2008 Pages: 151 - 152