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Cited by in F6Publishing
For: Starosta RT, Boyer S, Tahata S, Raymond K, Lee HE, Wolfe LA, Lam C, Edmondson AC, Schwartz IVD, Morava E. Liver manifestations in a cohort of 39 patients with congenital disorders of glycosylation: pin-pointing the characteristics of liver injury and proposing recommendations for follow-up. Orphanet J Rare Dis 2021;16:20. [PMID: 33413482 DOI: 10.1186/s13023-020-01630-2] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Johnsen C, Edmondson AC. Manifestations and Management of Hepatic Dysfunction in Congenital Disorders of Glycosylation. Clin Liver Dis (Hoboken) 2021;18:54-66. [PMID: 34584669 DOI: 10.1002/cld.1105] [Reference Citation Analysis]
2 Lipiński P, Tylki-Szymańska A. Congenital Disorders of Glycosylation: What Clinicians Need to Know? Front Pediatr 2021;9:715151. [PMID: 34540767 DOI: 10.3389/fped.2021.715151] [Reference Citation Analysis]
3 Lipiński P, Bogdańska A, Socha P, Tylki-Szymańska A. Liver Involvement in Congenital Disorders of Glycosylation and Deglycosylation. Front Pediatr 2021;9:696918. [PMID: 34291020 DOI: 10.3389/fped.2021.696918] [Reference Citation Analysis]
4 Pi S, Gong J, Xiao W, Xiao B, Mao X, Long H. The second DDOST-CDG patient with lactose intolerance, developmental delay, and situs inversus totalis. J Hum Genet 2021. [PMID: 34462534 DOI: 10.1038/s10038-021-00974-2] [Reference Citation Analysis]