Short Communication
Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort
B. H. Maher, M. Kerr, H. C. Cox, J. C. MacMillan and P. J. Brimage, et al.
2012, Volume 13, Number 1, Pages 97-101
Original Article
Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47)
Peter Bauer, Esther Leshinsky-Silver, Lubov Blumkin, Nina Schlipf and Christopher Schröder, et al.
2012, Volume 13, Number 1, Pages 73-76
Short Communication
Neuroferritinopathy: a new inborn error of iron metabolism
Michael J. Keogh, Patricia Jonas, Alan Coulthard, Patrick F. Chinnery and John Burn
2012, Volume 13, Number 1, Pages 93-96
Original Article
Vincristine exacerbates asymptomatic Charcot–Marie–Tooth disease with a novel EGR2 mutation
Tomonori Nakamura, Akihiro Hashiguchi, Shinsuke Suzuki, Kimiharu Uozumi and Shoko Tokunaga, et al.
2012, Volume 13, Number 1, Pages 77-82
Original Article
Distinct DNA binding and transcriptional repression characteristics related to different ARX mutations
Ginam Cho, MacLean P. Nasrallah, Youngshin Lim and Jeffrey A. Golden
2012, Volume 13, Number 1, Pages 23-29
Short Communication
Genome-scale methylation analysis of Parkinson's disease patients' brains reveals DNA hypomethylation and increased mRNA expression of cytochrome P450 2E1
Oliver Kaut, Ina Schmitt and Ullrich Wüllner
2012, Volume 13, Number 1, Pages 87-91
Original Article
Pathomechanistic characterization of two exonic L1CAM variants located in trans in an obligate carrier of X-linked hydrocephalus
Mariola Marx, Simone Diestel, Muriel Bozon, Laura Keglowich and Nathalie Drouot, et al.
2012, Volume 13, Number 1, Pages 49-59
Original Article
Genotype–phenotype correlation in interstitial 6q deletions: a report of 12 new cases
Jill A. Rosenfeld, Dina Amrom, Eva Andermann, Frederick Andermann and Martin Veilleux, et al.
2012, Volume 13, Number 1, Pages 31-47
Original Article
New brain-specific beta-synuclein isoforms show expression ratio changes in Lewy body diseases
Katrin Beyer, Ana M. Munoz-Marmol, Carolina Sanz, Ruth Marginet-Flinch and Isidro Ferrer, et al.
2012, Volume 13, Number 1, Pages 61-72
Letter to the Editors
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. Prescott, Miriam J. Smith and D. Gareth Evans
2012, Volume 13, Number 1, Pages 103-104