RNA processing pathways in amyotrophic lateral sclerosis Marka van BlitterswijkJohn E. Landers REVIEW ARTICLE 27 March 2010 Pages: 275 - 290
Novel variants identified in methyl-CpG-binding domain genes in autistic individuals Holly N. CukierRaquel RabionetJohn R. Gilbert ORIGINAL ARTICLE 18 November 2009 Pages: 291 - 303
Analysis of exon dosage using MLPA in South African Parkinson's disease patients Rowena J. KeyserDebbie LombardSoraya Bardien ORIGINAL ARTICLE 15 December 2009 Pages: 305 - 312
Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19 K. G. MeilleurM. TraoréK. H. Fischbeck ORIGINAL ARTICLE 29 December 2009 Pages: 313 - 318
Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy Luis E. KolbZulfikar ArlierMurat Gunel ORIGINAL ARTICLE 15 January 2010 Pages: 319 - 325
Meta-analysis of association between variation in the PDE4D gene and ischemic cerebral infarction risk in Asian populations Xiaowei XuXia LiWenli Sheng ORIGINAL ARTICLE 25 February 2010 Pages: 327 - 333
Fine mapping of the chromosome 10q11-q21 linkage region in Alzheimer's disease cases and controls Margaret Daniele FallinMegan SzymanskiDimitrios Avramopoulos ORIGINAL ARTICLE 25 February 2010 Pages: 335 - 348
Molecular characterization of six Chinese families with m.3460G>A and Leber hereditary optic neuropathy Dandan YuXiaoyun JiaYong-Gang Yao ORIGINAL ARTICLE 16 March 2010 Pages: 349 - 356
L239F founder mutation in GDAP1 is associated with a mild Charcot–Marie–Tooth type 4C4 (CMT4C4) phenotype Dagmara KabzińskaHalina Strugalska-CynowskaAndrzej Kochański ORIGINAL ARTICLE 16 March 2010 Pages: 357 - 366
Questionable association between a monoamine oxidase A promoter polymorphism and sudden infant death syndrome Michael KlintscharChristian Heimbold LETTER TO THE EDITORS Open access 01 April 2010 Pages: 367 - 368