Transcriptional regulation of long-term potentiation Nicola BliimIryna Leshchyns’kaMichael Janitz Review Article 18 June 2016 Pages: 201 - 210
Cortical gene expression: prognostic value for seizure outcome following temporal lobectomy and amygdalohippocampectomy Matthew J. GallekJesse SkochMartin E. Weinand Original Article 02 June 2016 Pages: 211 - 218
A mutation in the THG1L gene in a family with cerebellar ataxia and developmental delay Simon EdvardsonYael Elbaz-AlonOrly Elpeleg Original Article 15 June 2016 Pages: 219 - 225
PARP10 deficiency manifests by severe developmental delay and DNA repair defect Maher Awni ShahrourClaudia M. NicolaeOrly Elpeleg Original Article 13 September 2016 Pages: 227 - 232
A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson’s disease Valentina La CognataGiovanna MorelloSebastiano Cavallaro Original Article Open access 17 September 2016 Pages: 233 - 244
A novel KCNA1 mutation in a family with episodic ataxia and malignant hyperthermia Tiago A. MestreAndreea ManoleGrace Yoon Short Communication 08 June 2016 Pages: 245 - 249
Polymicrogyria and myoclonic epilepsy in autosomal recessive cutis laxa type 2A Rony CohenAyelet HalevyRachel Straussberg Short Communication 08 September 2016 Pages: 251 - 257
New ATP8A2 gene mutations associated with a novel syndrome: encephalopathy, intellectual disability, severe hypotonia, chorea and optic atrophy Elena Martín-HernándezMaría Elena Rodríguez-GarcíaFrancisco Martínez-Azorín Short Communication 28 September 2016 Pages: 259 - 263
Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing Kishore R KumarG.M. WaliMark J Cowley Short Communication Open access 28 September 2016 Pages: 265 - 270