Whole genome expression profiling of the medial and lateral substantia nigra in Parkinson’s disease L. B. MoranD. C. DukeM. B. Graeber Original Article 12 January 2006 Pages: 1 - 11
Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern Brazil Hsin F. ChienChristan F. RohéVincenzo Bonifati Original Article 22 November 2005 Pages: 13 - 19
Death of neuronal clusters contributes to variance of age at onset in Huntington’s disease Branka ČajavecHanspeter HerzelSamuel Bernard Original Article 14 January 2006 Pages: 21 - 25
The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington’s disease Silke MetzgerPeter BauerOlaf Riess Original Article 21 December 2005 Pages: 27 - 30
PLP1 and GPM6B intragenic copy number analysis by MAPH in 262 patients with hypomyelinating leukodystrophies: identification of one partial triplication and two partial deletions of PLP1 Patricia CombesMarie-Noelle Bonnet-DupeyronCatherine Vaurs-Barrière Original Article 17 January 2006 Pages: 31 - 37
Screening of ARX in mental retardation families: consequences for the strategy of molecular diagnosis K. PoirierD. LacombeT. Bienvenu Original Article 19 October 2005 Pages: 39 - 46
Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegia Marcia A. BlairShaochun MaPeter Hedera Original Article 18 February 2006 Pages: 47 - 50
Introducing a novel human mtDNA mutation into the Paracoccus denitrificans COX I gene explains functional deficits in a patient Simona LucioliKlaus HoffmeierFilippo M. Santorelli Original Article 12 November 2005 Pages: 51 - 57
Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation Marco VenturinSilvia MonciniPaola Riva Original Article 20 January 2006 Pages: 59 - 66
