Search filters

List of works by Nurulamin Abu Bakar

A mutation in mannose-phosphate-dolichol utilization defect 1 reveals clinical symptoms of congenital disorders of glycosylation type I and dystroglycanopathy

scientific article published on 30 September 2019

Clinical glycomics for the diagnosis of congenital disorders of glycosylation.

scientific article

Intact transferrin and total plasma glycoprofiling for diagnosis and therapy monitoring in phosphoglucomutase-I deficiency

scientific article published on 10 May 2018

Integrating glycomics and genomics uncovers SLC10A7 as essential factor for bone mineralization by regulating post-Golgi protein transport and glycosylation

article published in 2018

Oral D-galactose supplementation in PGM1-CDG.

scientific article published on 15 June 2017

PGM1 deficiency: Substrate use during exercise and effect of treatment with galactose.

scientific article published on 19 January 2017

Sialic acid catabolism by N-acetylneuraminate pyruvate lyase is essential for muscle function

scientific article published on 20 December 2018

Paulina is supported by:

About Paulina

Help