OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Mass Spectrometry of Transferrin and Apolipoprotein CIII from Dried Blood Spots for Congenital Disorders of Glycosylation
Yoshinao Wada, Machiko Kadoya, Nobuhiko Okamoto
Mass Spectrometry (2022) Vol. 11, Iss. 1, pp. A0113-A0113
Open Access | Times Cited: 6
Yoshinao Wada, Machiko Kadoya, Nobuhiko Okamoto
Mass Spectrometry (2022) Vol. 11, Iss. 1, pp. A0113-A0113
Open Access | Times Cited: 6
Showing 6 citing articles:
Mass Spectrometry as a First-Line Diagnostic Aid for Congenital Disorders of Glycosylation
Yoshinao Wada
Mass Spectrometry (2025) Vol. 14, Iss. 1, pp. A0169-A0169
Open Access | Times Cited: 1
Yoshinao Wada
Mass Spectrometry (2025) Vol. 14, Iss. 1, pp. A0169-A0169
Open Access | Times Cited: 1
Biochemical diagnosis of congenital disorders of glycosylation
Alexandre Raynor, Walid Haouari, Elodie Lebredonchel, et al.
Advances in clinical chemistry (2024), pp. 1-43
Closed Access | Times Cited: 5
Alexandre Raynor, Walid Haouari, Elodie Lebredonchel, et al.
Advances in clinical chemistry (2024), pp. 1-43
Closed Access | Times Cited: 5
Biochemical testing for congenital disorders of glycosylation: A technical standard of the American College of Medical Genetics and Genomics (ACMG)
Patricia Hall, Christina Lam, Lynne A. Wolfe, et al.
Genetics in Medicine (2025), pp. 101328-101328
Closed Access
Patricia Hall, Christina Lam, Lynne A. Wolfe, et al.
Genetics in Medicine (2025), pp. 101328-101328
Closed Access
Diagnostic and Therapeutic Approaches in Congenital Disorders of Glycosylation
Alexandre Raynor, Élodie Lebredonchel, François Foulquier, et al.
Handbook of experimental pharmacology (2025)
Closed Access
Alexandre Raynor, Élodie Lebredonchel, François Foulquier, et al.
Handbook of experimental pharmacology (2025)
Closed Access
Progressive myoclonic epilepsy as an expanding phenotype of NGLY1-associated congenital deglycosylation disorder: A case report and review of the literature
Yuri Sonoda, Atsushi Fujita, Michiko Torio, et al.
European Journal of Medical Genetics (2023) Vol. 67, pp. 104895-104895
Open Access | Times Cited: 5
Yuri Sonoda, Atsushi Fujita, Michiko Torio, et al.
European Journal of Medical Genetics (2023) Vol. 67, pp. 104895-104895
Open Access | Times Cited: 5
Quantitative Assessment of Core Fucosylation for Congenital Disorders of Glycosylation
Yoshinao Wada, Machiko Kadoya
Mass Spectrometry (2024) Vol. 13, Iss. 1, pp. A0159-A0159
Open Access | Times Cited: 1
Yoshinao Wada, Machiko Kadoya
Mass Spectrometry (2024) Vol. 13, Iss. 1, pp. A0159-A0159
Open Access | Times Cited: 1
