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For: Woods AG, Woods CW, Snow TM. Congenital disorders of glycosylation. Adv Neonatal Care 2012;12:90-5. [PMID: 22469961 DOI: 10.1097/ANC.0b013e318241cb20] [Cited by in Crossref: 15] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
Number Citing Articles
1 Murali C, Lu JT, Jain M, Liu DS, Lachman R, Gibbs RA, Lee BH, Cohn D, Campeau PM. Diagnosis of ALG12-CDG by exome sequencing in a case of severe skeletal dysplasia. Mol Genet Metab Rep 2014;1:213-9. [PMID: 25019053 DOI: 10.1016/j.ymgmr.2014.04.004] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 2.0] [Reference Citation Analysis]
2 Ednie AR, Harper JM, Bennett ES. Sialic acids attached to N- and O-glycans within the Nav1.4 D1S5-S6 linker contribute to channel gating. Biochim Biophys Acta 2015;1850:307-17. [PMID: 25450184 DOI: 10.1016/j.bbagen.2014.10.027] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 0.9] [Reference Citation Analysis]
3 Dhaunsi GS. Receptor-mediated selective impairment of insulin-like growth factor-1 activity in congenital disorders of glycosylation patients. Pediatr Res 2017;81:526-30. [PMID: 27089502 DOI: 10.1038/pr.2016.96] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
4 Panigrahy N, Lingappa L, Ramadevi AR, Venkatlakshmi A. Congenital Disorder of Glycosylation (CDG) Presenting as Non-immune Hydrops Fetalis. Indian J Pediatr 2016;83:359-60. [PMID: 26365158 DOI: 10.1007/s12098-015-1895-z] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
5 Dolitsky S, Mitra A, Khan S, Ashkinadze E, Sauer MV. Beyond the "Jewish panel": the importance of offering expanded carrier screening to the Ashkenazi Jewish population. F S Rep 2020;1:294-8. [PMID: 34223259 DOI: 10.1016/j.xfre.2020.08.001] [Reference Citation Analysis]