Milestones in Friedreich ataxia: more than a century and still learning Agessandro AbrahãoJosé Luiz PedrosoOrlando Graziani Povoas Barsottini Review article 08 February 2015 Pages: 151 - 160
Multiple sclerosis risk loci correlate with cervical cord atrophy and may explain the course of disability Denis A. AkkadBarbara BellenbergAiden Haghikia Original Article 27 January 2015 Pages: 161 - 168
Association of a common genetic variant within ANKK1 with six-month cognitive performance after traumatic brain injury John K. YueAngela M. ProngerThe TRACK-TBI Investigators Original Article 30 January 2015 Pages: 169 - 180
Genetic ablation of ataxin-2 increases several global translation factors in their transcript abundance but decreases translation rate M. FittschenI. Lastres-BeckerG. Auburger Original Article Open access 27 February 2015 Pages: 181 - 192
A start codon CMT1X mutation associated with transient encephalomyelitis causes complete loss of Cx32 Irene SargiannidouGun-Ha KimKleopas A. Kleopa Original Article 15 March 2015 Pages: 193 - 200
Long intervening non-coding RNA 00320 is human brain-specific and highly expressed in the cortical white matter James D. MillsJieqiong ChenMichael Janitz Original Article 29 March 2015 Pages: 201 - 213
A defect in the retromer accessory protein, SNX27, manifests by infantile myoclonic epilepsy and neurodegeneration Nadirah DamsehChris M. DansonOrly Elpeleg Original Article 17 April 2015 Pages: 215 - 221
The fused in sarcoma protein forms cytoplasmic aggregates in motor neurons derived from integration-free induced pluripotent stem cells generated from a patient with familial amyotrophic lateral sclerosis carrying the FUS-P525L mutation Xinxiu LiuJiayu ChenMin Deng Original Article 26 April 2015 Pages: 223 - 231
A novel frameshift mutation in FGF14 causes an autosomal dominant episodic ataxia Karine ChoquetRoberta La PianaBernard Brais Short Communication 08 January 2015 Pages: 233 - 236
MRPS22 mutation causes fatal neonatal lactic acidosis with brain and heart abnormalities Fabian BaertlingTobias B. HaackFelix Distelmaier Short Communication 10 February 2015 Pages: 237 - 240
Mitochondrial serine protease HTRA2 gene mutation in Asians with coexistent essential tremor and Parkinson disease Yin Xia ChaoEbonne Yulin NgEng-King Tan Letter to the Editors 20 March 2015 Pages: 241 - 242
Erratum to: The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together A. DuarriE. NibbelingD. S. Verbeek Erratum 12 April 2015 Pages: 243 - 243