Eur. J. Paediatr. Neurol.

SLC35A2-related congenital disorder of glycosylation: Defining the phenotype.

Yates TM, Suri M, Desurkar A, ..., Thuresson AC, Balasubramanian M

Eur. J. Paediatr. Neurol. 22 (6) 1095-1102 [2018-11-00; online 2018-08-27]

Biotin and Thiamine Responsive Basal Ganglia Disease--A vital differential diagnosis in infants with severe encephalopathy.

Ygberg S, Naess K, Eriksson M, ..., Wedell A, Wickström R

Eur. J. Paediatr. Neurol. 20 (3) 457-461 [2016-05-00; online 2016-02-04]

Affiliated researcher