Nurulamin Abu Bakar - Concepedia

Author

Nurulamin Abu Bakar

Radboud University Medical Center ORCID

Also Known As

A. Abu Bakar, Abu Bakar, Nurulamin, N. Abu Bakar, N. Bakar, Nurulamin Abu Bakar

Publications

404

Citations

H-Index

Concepts

All Affiliations

Radboud University Medical Center Radboud University Nijmegen Heidelberg University Zentrum für Kinderheilkunde Mayo Clinic

About

Nurulamin Abu Bakar is an author at Radboud University Medical Center specializing in medicine, diabetes, and glycobiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	198
2	Health Sciences	2	2	94
3	Biochemistry	2	2	80
4	Diabetes	2	2	118
5	Cell Biology	1	1	40

Nurulamin Abu Bakar

Publications

333

Citations

H-Index

Page 1

	Year	Citations
Oral D-galactose supplementation in PGM1-CDG Sunnie Wong, Therese Gadomski, Monique van Scherpenzeel, Genetics in Medicine MedicineDiabetesOral D-galactose SupplementationPharmacologyCarbohydrate-protein Interaction	2017	78
Integrating glycomics and genomics uncovers SLC10A7 as essential factor for bone mineralization by regulating post-Golgi protein transport and glycosylation Angel Ashikov, Nurulamin Abu Bakar, Xiao‐Yan Wen, Human Molecular Genetics	2018	63
Sialic acid catabolism by N-acetylneuraminate pyruvate lyase is essential for muscle function Xiao‐Yan Wen, Maja Tarailo‐Graovac, Koroboshka Brand‐Arzamendi, JCI Insight Muscle FunctionSialic Acid BiosynthesisGlycobiologyBiosynthesisSkeletal Muscle	2018	54
PGM1 deficiency: Substrate use during exercise and effect of treatment with galactose Nicol C. Voermans, Nicolai Preisler, Karen L. Madsen, Neuromuscular Disorders NutritionEnergy MetabolismHealth SciencesExercise PhysiologyPhysiology	2017	40
Phosphoglucomutase-1 deficiency: Early presentation, metabolic management and detection in neonatal blood spots Federica Conte, Éva Morava, Nurulamin Abu Bakar, Molecular Genetics and Metabolism	2020	33
Intact transferrin and total plasma glycoprofiling for diagnosis and therapy monitoring in phosphoglucomutase-I deficiency Nurulamin Abu Bakar, Nicol C. Voermans, Thorsten Marquardt, Translational research Intact TransferrinBiochemistryTherapy MonitoringMedicineChronic Kidney Disease	2018	26
Synergistic use of glycomics and single‐molecule molecular inversion probes for <scp>identification</scp> of congenital disorders of glycosylation type‐1 Nurulamin Abu Bakar, Angel Ashikov, Jaime Moritz Brum, Journal of Inherited Metabolic Disease	2022	21
A mutation in mannose‐phosphate‐dolichol utilization defect 1 reveals clinical symptoms of congenital disorders of glycosylation type I and dystroglycanopathy Walinka van Tol, Angel Ashikov, Eckhard Korsch, JIMD Reports	2019	18

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