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For: Amirneni S, Haep N, Gad MA, Soto-Gutierrez A, Squires JE, Florentino RM. Molecular overview of progressive familial intrahepatic cholestasis. World J Gastroenterol 2020; 26(47): 7470-7484 [PMID: 33384548 DOI: 10.3748/wjg.v26.i47.7470] [Cited by in CrossRef: 6] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Sánchez-Monteagudo A, Ripollés E, Berenguer M, Espinós C. Wilson's Disease: Facing the Challenge of Diagnosing a Rare Disease. Biomedicines 2021;9:1100. [PMID: 34572285 DOI: 10.3390/biomedicines9091100] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
2 Jagadisan B, Dhawan A. Emergencies in Pediatric hepatology. J Hepatol 2022:S0168-8278(21)02304-7. [PMID: 34990749 DOI: 10.1016/j.jhep.2021.12.027] [Reference Citation Analysis]
3 Florentino RM, Li Q, Coard MC, Haep N, Motomura T, Diaz-Aragon R, Faccioli LAP, Amirneni S, Kocas-Kilicarslan ZN, Ostrowska A, Squires JE, Feranchak AP, Soto-Gutierrez A. Transmembrane channel activity in human hepatocytes and cholangiocytes derived from induced pluripotent stem cells. Hepatol Commun 2022. [PMID: 35289126 DOI: 10.1002/hep4.1920] [Reference Citation Analysis]
4 Liu TF, He JJ, Wang L, Zhang LY. Novel ABCB4 mutations in an infertile female with progressive familial intrahepatic cholestasis type 3: A case report. World J Clin Cases 2022; 10(6): 1998-2006 [DOI: 10.12998/wjcc.v10.i6.1998] [Reference Citation Analysis]
5 Tang J, Tan M, Deng Y, Tang H, Shi H, Li M, Ma W, Li J, Dai H, Li J, Zhou S, Li X, Wei F, Ma X, Luo L. Two Novel Pathogenic Variants of TJP2 Gene and the Underlying Molecular Mechanisms in Progressive Familial Intrahepatic Cholestasis Type 4 Patients. Front Cell Dev Biol 2021;9:661599. [PMID: 34504838 DOI: 10.3389/fcell.2021.661599] [Reference Citation Analysis]
6 Mahle AC, Morris BD, Frazer Z, Novak C. Severe vitamin deficiencies in pregnancy complicated by progressive familial intrahepatic cholestasis. BMJ Case Rep 2021;14:e240248. [PMID: 33692058 DOI: 10.1136/bcr-2020-240248] [Reference Citation Analysis]
7 Moussaoui S, Abdelwahed M, Ben Chaaben N, Bellalah A, Ben Fadhel N, Guediche A, Zakhama M, Tababi R, Aouam K, Abdelfattah Z, Loghmari H, Safer L. Norethisterone‐induced cholestasis: A case report. Clinical Case Reports 2022;10. [DOI: 10.1002/ccr3.5522] [Reference Citation Analysis]
8 Bolia R, Goel AD, Sharma V, Srivastava A. Biliary Diversion in Progressive Familial Intrahepatic Cholestasis: A Systematic Review and Meta-Analysis. Expert Rev Gastroenterol Hepatol 2022. [PMID: 35051344 DOI: 10.1080/17474124.2022.2032660] [Reference Citation Analysis]
9 Pan Q, Luo G, Qu J, Chen S, Zhang X, Zhao N, Ding J, Yang H, Li M, Li L, Cheng Y, Li X, Xie Q, Li Q, Zhou X, Zou H, Fan S, Zou L, Liu W, Deng G, Cai SY, Boyer JL, Chai J. A homozygous R148W mutation in Semaphorin 7A causes progressive familial intrahepatic cholestasis. EMBO Mol Med 2021;13:e14563. [PMID: 34585848 DOI: 10.15252/emmm.202114563] [Reference Citation Analysis]
10 Vij M, Shah V. Compound Heterozygous Myosin 5B (Myo5b) Mutation with Early Onset Progressive Cholestasis and No Intestinal Failure. Fetal Pediatr Pathol 2021;:1-7. [PMID: 34338607 DOI: 10.1080/15513815.2021.1959690] [Reference Citation Analysis]