Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri Pepijn van den MunckhofImke ChristiaansTheo J. M. Hulsebos ORIGINAL ARTICLE 26 October 2011 Pages: 1 - 7
Restriction of trophic factors and nutrients induces PARKIN expression M. KlinkenbergS. GispertM. Jendrach ORIGINAL ARTICLE Open access 26 October 2011 Pages: 9 - 21
Distinct DNA binding and transcriptional repression characteristics related to different ARX mutations Ginam ChoMacLean P. NasrallahJeffrey A. Golden Original Article 18 January 2012 Pages: 23 - 29
Genotype–phenotype correlation in interstitial 6q deletions: a report of 12 new cases Jill A. RosenfeldDina AmromLisa G. Shaffer Original Article 05 January 2012 Pages: 31 - 47
Pathomechanistic characterization of two exonic L1CAM variants located in trans in an obligate carrier of X-linked hydrocephalus Mariola MarxSimone DiestelMichael K. E. Schäfer Original Article 06 January 2012 Pages: 49 - 59
New brain-specific beta-synuclein isoforms show expression ratio changes in Lewy body diseases Katrin BeyerAna M. Munoz-MarmolAurelio Ariza Original Article 29 December 2011 Pages: 61 - 72
Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47) Peter BauerEsther Leshinsky-SilverLudger Schöls Original Article 31 January 2012 Pages: 73 - 76
Vincristine exacerbates asymptomatic Charcot–Marie–Tooth disease with a novel EGR2 mutation Tomonori NakamuraAkihiro HashiguchiHiroshi Takashima Original Article 25 January 2012 Pages: 77 - 82
Independent replication of STAT3 association with multiple sclerosis risk in a large German case–control sample Christina M. LillBrit-Maren M. SchjeideFrauke Zipp Short Communication 18 November 2011 Pages: 83 - 86
Genome-scale methylation analysis of Parkinson's disease patients' brains reveals DNA hypomethylation and increased mRNA expression of cytochrome P450 2E1 Oliver KautIna SchmittUllrich Wüllner Short Communication 12 January 2012 Pages: 87 - 91
Neuroferritinopathy: a new inborn error of iron metabolism Michael J. KeoghPatricia JonasJohn Burn Short Communication 26 January 2012 Pages: 93 - 96
Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort B. H. MaherM. KerrL. R. Griffiths Short Communication 01 February 2012 Pages: 97 - 101
Comment on the article “Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri” by van den Munckhof et al. Trine E. PrescottMiriam J. SmithD. Gareth Evans Letter to the Editors 28 December 2011 Pages: 103 - 104