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For: Elkadri AA. Congenital Diarrheal Syndromes. Clin Perinatol 2020;47:87-104. [PMID: 32000931 DOI: 10.1016/j.clp.2019.10.010] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
Number Citing Articles
1 Babcock SJ, Flores-marin D, Thiagarajah JR. The genetics of monogenic intestinal epithelial disorders. Hum Genet 2022. [DOI: 10.1007/s00439-022-02501-5] [Reference Citation Analysis]
2 Hoşnut FÖ, Sahin GE, Ozyazıcı A, Olgac A, Aksu AU. Congenital Rare Diseases Causing Persistent Diarrhea in the Newborn: A Single Center Experience. Z Geburtshilfe Neonatol 2022. [PMID: 35576965 DOI: 10.1055/a-1774-5005] [Reference Citation Analysis]
3 Jonathan Medernach, Middleton JP. Malabsorption Syndromes and Food Intolerance. Clinics in Perinatology 2022. [DOI: 10.1016/j.clp.2022.02.015] [Reference Citation Analysis]
4 Yan W, Xiao Y, Zhang Y, Tao Y, Cao Y, Liu K, Cai W, Wang Y. Monogenic mutations in four cases of neonatal-onset watery diarrhea and a mutation review in East Asia. Orphanet J Rare Dis 2021;16:383. [PMID: 34503561 DOI: 10.1186/s13023-021-01995-y] [Reference Citation Analysis]
5 Qian Y, Wu B, Liu R, Lu Y, Zhang P, Shao C, Huang Y, Wang H. Case Report: Complete Maternal Uniparental Isodisomy of Chromosome 5 (iUPD(5)mat) With PCSK1 Nonsense Variant in an Infant With Recurrent Diarrhea. Front Genet 2021;12:668326. [PMID: 34025722 DOI: 10.3389/fgene.2021.668326] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Bandyopadhyay T, Deswal S, Maria A, Phulware RH, Das P, Ahuja A. Microvillous inclusion disease as a cause of severe congenital diarrhea in a newborn. J Matern Fetal Neonatal Med 2021;:1-3. [PMID: 33843415 DOI: 10.1080/14767058.2021.1910656] [Reference Citation Analysis]