The following new article has just been published in Orphanet Journal of Rare Diseases

RESEARCH
Brain morphometry in Pontocerebellar Hypoplasia type 2
Kaspar Ekert, Samuel Groeschel, Iciar Sánchez-Albisua, Saskia Frölich, Andrea Dieckmann, Corinna Engel and Ingeborg Krägeloh-Mann
Published on: 19 July 2016
RESEARCH
Analysis of voice quality in patients with late-onset Pompe disease
Krzysztof Szklanny, Ryszard Gubrynowicz, Katarzyna Iwanicka-Pronicka and Anna Tylki-Szymańska
Published on: 15 July 2016
RESEARCH
Health survey of adults with hereditary spastic paraparesis compared to population study controls
Krister W. Fjermestad, Øivind J. Kanavin, Eva E. Næss, Lise B. Hoxmark and Grete Hummelvoll
Published on: 13 July 2016
RESEARCH
Mucopolysaccharidosis I; Parental beliefs about the impact of disease on the quality of life of their children
A. Soni-Jaiswal, J. Mercer, S. A. Jones, I. A. Bruce and P. Callery
Published on: 12 July 2016
RESEARCH
Whole exome sequencing diagnosis of inborn errors of metabolism and other disorders in United Arab Emirates
Aisha Al-Shamsi, Jozef L. Hertecant, Abdul-Kader Souid and Fatma A. Al-Jasmi
Published on: 8 July 2016