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170 related items for PubMed ID: 37137858

  • 1. [Clinical and genetic analysis of cases of progressive familial intrahepatic cholestasis type 3].
    Shen YL, Zhang XT, Xun YH.
    Zhonghua Gan Zang Bing Za Zhi; 2023 Mar 20; 31(3):307-313. PubMed ID: 37137858
    [Abstract] [Full Text] [Related]

  • 2. Progressive familial intrahepatic cholestasis type 3: Report of four clinical cases, novel ABCB4 variants and long-term follow-up.
    Lipiński P, Ciara E, Jurkiewicz D, Płoski R, Wawrzynowicz-Syczewska M, Pawłowska J, Jankowska I.
    Ann Hepatol; 2021 Mar 20; 25():100342. PubMed ID: 33757843
    [Abstract] [Full Text] [Related]

  • 3. [Clinical and genetic analysis of a family affected by progressive familial intraphepatic cholestasis type 3].
    Deng M, Guo L, Song Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Oct 10; 35(5):686-690. PubMed ID: 30298496
    [Abstract] [Full Text] [Related]

  • 4. [Clinical phenotype and genotype analysis of progressive familial intrahepatic cholestasis type 3 caused by novel ABCB4 gene mutation].
    Ye XL, Yu FH, Zhou J, Zhao CN, Wu J.
    Zhonghua Er Ke Za Zhi; 2024 Jul 02; 62(7):649-654. PubMed ID: 38955683
    [Abstract] [Full Text] [Related]

  • 5. A novel heterozygous deletion in ABCB4 gene in a Chinese family with intrahepatic cholestasis of pregnancy, neonatal hyperbilirubinemia, and cholelithiasis: Case reports and literature review.
    Zheng Y, Rao Q, Han Y, He J.
    Mol Genet Genomic Med; 2024 Jan 02; 12(1):e2291. PubMed ID: 37787087
    [Abstract] [Full Text] [Related]

  • 6. Cryptogenic cholestasis in young and adults: ATP8B1, ABCB11, ABCB4, and TJP2 gene variants analysis by high-throughput sequencing.
    Vitale G, Gitto S, Raimondi F, Mattiaccio A, Mantovani V, Vukotic R, D'Errico A, Seri M, Russell RB, Andreone P.
    J Gastroenterol; 2018 Aug 02; 53(8):945-958. PubMed ID: 29238877
    [Abstract] [Full Text] [Related]

  • 7. Heterozygous mutations of ATP8B1, ABCB11 and ABCB4 cause mild forms of Progressive Familial Intrahepatic Cholestasis in a pediatric cohort.
    Mínguez Rodríguez B, Molera Busoms C, Martorell Sampol L, García Romero R, Colomé Rivero G, Martín de Carpi J.
    Gastroenterol Hepatol; 2022 Oct 02; 45(8):585-592. PubMed ID: 34942279
    [Abstract] [Full Text] [Related]

  • 8. Evaluation of a Novel Missense Mutation in ABCB4 Gene Causing Progressive Familial Intrahepatic Cholestasis Type 3.
    Saleem K, Cui Q, Zaib T, Zhu S, Qin Q, Wang Y, Dam J, Ji W, Liu P, Jia X, Wu J, Bai J, Fu S, Sun W.
    Dis Markers; 2020 Oct 02; 2020():6292818. PubMed ID: 32626542
    [Abstract] [Full Text] [Related]

  • 9. A novel compound heterozygous mutation in ABCB4 gene in a pedigree with progressive familial intrahepatic cholestasis 3: a case report.
    Bai J, Li L, Liu H, Liu S, Bai L, Ning H, Song W, Zou H, Wang X, Chen Y, Zheng S, Duan Z.
    Ann Transl Med; 2021 Mar 02; 9(5):426. PubMed ID: 33842647
    [Abstract] [Full Text] [Related]

  • 10. Familial intrahepatic cholestasis: New and wide perspectives.
    Vitale G, Gitto S, Vukotic R, Raimondi F, Andreone P.
    Dig Liver Dis; 2019 Jul 02; 51(7):922-933. PubMed ID: 31105019
    [Abstract] [Full Text] [Related]

  • 11. Case Report: A rare case of young adult progressive familial intrahepatic cholestasis-type 3 with a novel heterozygous pathogenic variant of ABCB4.
    Zhu H, Wang S, Li L, Geng W, Wan X, Hua R, Wang D, Gao P.
    Front Pediatr; 2022 Jul 02; 10():1012825. PubMed ID: 36330364
    [Abstract] [Full Text] [Related]

  • 12. ABCB4 Mutations in Adults Cause a Spectrum Cholestatic Disorder Histologically Distinct from Other Biliary Disease.
    Sinha A, Bhuva M, Grant C, Gimson AE, Thompson E, Duckworth A, Davies SE, Aithal G, Griffiths WJ.
    Dig Dis Sci; 2022 Dec 02; 67(12):5551-5561. PubMed ID: 35288833
    [Abstract] [Full Text] [Related]

  • 13. The molecular landscape of progressive familial intrahepatic cholestasis in Turkey: Defining the molecular profiles and expanding the variant spectrum.
    Bakır A, Topçu V, Çavdarlı B.
    Ann Hum Genet; 2022 May 02; 86(3):119-126. PubMed ID: 34961929
    [Abstract] [Full Text] [Related]

  • 14. Spectrum of genomic variations in Indian patients with progressive familial intrahepatic cholestasis.
    Sharma A, Poddar U, Agnihotry S, Phadke SR, Yachha SK, Aggarwal R.
    BMC Gastroenterol; 2018 Jul 04; 18(1):107. PubMed ID: 29973134
    [Abstract] [Full Text] [Related]

  • 15. [Analysis of clinical characteristic of children with progressive familial intrahepatic cholestasis type 3].
    Cao LL, Yan JG, Feng DN, Dong Y, Xu ZQ, Wang FC, Gao YJ, Zhu SS, Zhang M.
    Zhonghua Er Ke Za Zhi; 2024 May 02; 62(5):462-466. PubMed ID: 38623015
    [Abstract] [Full Text] [Related]

  • 16. Familial cholestasis: progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy.
    van der Woerd WL, van Mil SW, Stapelbroek JM, Klomp LW, van de Graaf SF, Houwen RH.
    Best Pract Res Clin Gastroenterol; 2010 Oct 02; 24(5):541-53. PubMed ID: 20955958
    [Abstract] [Full Text] [Related]

  • 17. NR1H4 analysis in patients with progressive familial intrahepatic cholestasis, drug-induced cholestasis or intrahepatic cholestasis of pregnancy unrelated to ATP8B1, ABCB11 and ABCB4 mutations.
    Davit-Spraul A, Gonzales E, Jacquemin E.
    Clin Res Hepatol Gastroenterol; 2012 Dec 02; 36(6):569-73. PubMed ID: 23142591
    [Abstract] [Full Text] [Related]

  • 18. Molecular characterization of exons 6, 8 and 9 of ABCB4 gene in children with Progressive Familial Intrahepatic Cholestasis type 3.
    Fathy M, Kamal M, Al-Sharkawy M, Al-Karaksy H, Hassan N.
    Biomarkers; 2016 Nov 02; 21(7):573-7. PubMed ID: 27075526
    [Abstract] [Full Text] [Related]

  • 19. Novel ABCB4 mutation in a Chinese female patient with progressive familial intrahepatic cholestasis type 3: a case report.
    Wu Z, Zhang S, Zhang L, Li M.
    Diagn Pathol; 2020 Apr 22; 15(1):39. PubMed ID: 32321542
    [Abstract] [Full Text] [Related]

  • 20. Expanding the spectrum of progressive familial intrahepatic cholestasis: A report of 3 cases.
    Jiao J, Morotti R, Shafizadeh N, Jain D.
    Am J Clin Pathol; 2024 Sep 27. PubMed ID: 39333837
    [Abstract] [Full Text] [Related]

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