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For: Bruneel A, Cholet S, Tran NT, Mai TD, Fenaille F. CDG biochemical screening: Where do we stand? Biochimica et Biophysica Acta (BBA) - General Subjects 2020;1864:129652. [DOI: 10.1016/j.bbagen.2020.129652] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
Number Citing Articles
1 Raynor A, Haouari W, Ng BG, Cholet S, Harroche A, Raulet-Bussian C, Lounis-Ouaras S, Vuillaumier-Barrot S, Pascreau T, Borgel D, Freeze HH, Fenaille F, Bruneel A. SLC37A4-CDG: New biochemical insights for an emerging congenital disorder of glycosylation with major coagulopathy. Clin Chim Acta 2021;521:104-6. [PMID: 34245688 DOI: 10.1016/j.cca.2021.07.005] [Reference Citation Analysis]
2 Raynor A, Vincent-Delorme C, Alaix AS, Cholet S, Dupré T, Vuillaumier-Barrot S, Fenaille F, Besmond C, Bruneel A. Normal transferrin patterns in congenital disorders of glycosylation with Golgi homeostasis disruption: apolipoprotein C-III at the rescue! Clin Chim Acta 2021;519:285-90. [PMID: 34022244 DOI: 10.1016/j.cca.2021.05.016] [Reference Citation Analysis]
3 Castiglioni C, Feillet F, Barnerias C, Wiedemann A, Muchart J, Cortes F, Hernando-Davalillo C, Montero R, Dupré T, Bruneel A, Seta N, Vuillaumier-Barrot S, Serrano M. Expanding the phenotype of X-linked SSR4-CDG: Connective tissue implications. Hum Mutat 2021;42:142-9. [PMID: 33300232 DOI: 10.1002/humu.24151] [Reference Citation Analysis]
4 Liénard-Mayor T, Yang B, Tran NT, Bruneel A, Guttman A, Taverna M, Mai TD. High sensitivity capillary electrophoresis with fluorescent detection for glycan mapping. J Chromatogr A 2021;1657:462593. [PMID: 34689907 DOI: 10.1016/j.chroma.2021.462593] [Reference Citation Analysis]
5 Sakhi S, Cholet S, Wehbi S, Isidor B, Cogne B, Vuillaumier-Barrot S, Dupré T, Detleft T, Schmitt E, Leheup B, Bonnet C, Feillet F, Muti C, Fenaille F, Bruneel A. MAN1B1-CDG: Three new individuals and associated biochemical profiles. Mol Genet Metab Rep 2021;28:100775. [PMID: 34141584 DOI: 10.1016/j.ymgmr.2021.100775] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Sierra T, Crevillen AG, Escarpa A. Electrochemical sensor for the assessment of carbohydrate deficient transferrin: Application to diagnosis of congenital disorders of glycosilation. Biosens Bioelectron 2021;179:113098. [PMID: 33636501 DOI: 10.1016/j.bios.2021.113098] [Reference Citation Analysis]
7 Lipiński P, Bogdańska A, Tylki-Szymańska A. Congenital disorders of glycosylation: Prevalence, incidence and mutational spectrum in the Polish population. Mol Genet Metab Rep 2021;27:100726. [PMID: 33643843 DOI: 10.1016/j.ymgmr.2021.100726] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]