Risk for multiple sclerosis in relatives and spouses of patients diagnosed with autoimmune and related conditions Kari HemminkiXinjun LiKristina Sundquist Original Article 09 October 2008 Pages: 5 - 11
Alzheimer’s disease risk variants show association with cerebrospinal fluid amyloid beta John S. K. KauweJun WangAlison M. Goate Original Article 24 September 2008 Pages: 13 - 17
Assessment of Alzheimer’s disease case–control associations using family-based methods Brit-Maren M. SchjeideMatthew B. McQueenLars Bertram Original Article 02 October 2008 Pages: 19 - 25
Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation Lena SkoglundRoseMarie BrundinAnna Glaser Original Article 15 October 2008 Pages: 27 - 34
A locus for bilateral occipital polymicrogyria maps to chromosome 6q16–q22 Bouchra Ouled Amar Ben CheikhStéphanie BaulacEric LeGuern Original Article 29 August 2008 Pages: 35 - 42
Identification of a heterozygous genomic deletion in the spatacsin gene in SPG11 patients using high-resolution comparative genomic hybridization Peter BauerBeate WinnerLudger Schöls Original Article 12 September 2008 Pages: 43 - 48
Molecular and functional analysis of the HEXB gene in Italian patients affected with Sandhoff disease: identification of six novel alleles Stefania ZampieriMirella FilocamoAndrea Dardis Original Article 29 August 2008 Pages: 49 - 58
Maternal uniparental heterodisomy with partial isodisomy of a chromosome 2 carrying a splice acceptor site mutation (IVS9–2A>T) in ALS2 causes infantile-onset ascending spastic paralysis (IAHSP) Thilo HerzfeldNicole WolfUlrich Müller Original Article 23 September 2008 Pages: 59 - 64
Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis Laura FilonziCinzia MagnaniFrancesco Nonnis Marzano Original Article 23 September 2008 Pages: 65 - 72
A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis E. StogmannS. El TawilA. Zimprich Original Article 11 October 2008 Pages: 73 - 77
Expression analysis of genes lying in the NF1 microdeletion interval points to four candidate modifiers for neurofibroma formation B. Bartelt-KirbachM. WueppingD. Kaufmann Short Communication 11 October 2008 Pages: 79 - 85
Erratum to ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia Sascha VermeerRowdy P. P. MeijerBerry Kremer Erratum 24 October 2008 Pages: 87 - 87