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Journal Abstract Search


277 related items for PubMed ID: 9039994

  • 21. [Alagille Syndrome].
    Wakim El-Khoury J, Venetz JP, Rutz T, Sciarra A, Unger S, Sempoux C, Moradpour D, Fraga M.
    Rev Med Suisse; 2019 Aug 28; 15(660):1506-1510. PubMed ID: 31496175
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  • 22. Alagille syndrome: an uncommon cause of intrahepatic cholestasis in adults.
    Zhang W, Zhao X, Huang J, Ou X, Jia J.
    Rev Esp Enferm Dig; 2019 Apr 28; 111(4):323-326. PubMed ID: 30746957
    [Abstract] [Full Text] [Related]

  • 23. Alagille syndrome: an overview.
    Vajro P, Ferrante L, Paolella G.
    Clin Res Hepatol Gastroenterol; 2012 Jun 28; 36(3):275-7. PubMed ID: 22521120
    [Abstract] [Full Text] [Related]

  • 24. Alagille Syndrome: An Overview.
    Jesina D.
    Neonatal Netw; 2017 Nov 01; 36(6):343-347. PubMed ID: 29185945
    [Abstract] [Full Text] [Related]

  • 25. Alagille syndrome today.
    Alagille D.
    Clin Invest Med; 1996 Oct 01; 19(5):325-30. PubMed ID: 8889270
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  • 26. Alagille syndrome: clinical perspectives.
    Saleh M, Kamath BM, Chitayat D.
    Appl Clin Genet; 2016 Oct 01; 9():75-82. PubMed ID: 27418850
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  • 27. [Butterfly vertebrae and scoliosis: Alagille syndrome].
    Przkora R, Schmitz A, Perlick L, Koenig R, Jaeger U, Schmitt O.
    Z Orthop Ihre Grenzgeb; 2002 Oct 01; 140(2):182-4. PubMed ID: 12029591
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  • 28. Facial features in Alagille syndrome: specific or cholestasis facies?
    Kamath BM, Loomes KM, Oakey RJ, Emerick KE, Conversano T, Spinner NB, Piccoli DA, Krantz ID.
    Am J Med Genet; 2002 Oct 01; 112(2):163-70. PubMed ID: 12244550
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  • 29. Molecular analysis of 24 Alagille syndrome families identifies a single submicroscopic deletion and further localizes the Alagille region within 20p12.
    Rand EB, Spinner NB, Piccoli DA, Whitington PF, Taub R.
    Am J Hum Genet; 1995 Nov 01; 57(5):1068-73. PubMed ID: 7485156
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  • 30. Alagille syndrome and the Jagged1 gene.
    Piccoli DA, Spinner NB.
    Semin Liver Dis; 2001 Nov 01; 21(4):525-34. PubMed ID: 11745040
    [Abstract] [Full Text] [Related]

  • 31. Cytologically balanced t(2;20) in a two-generation family with alagille syndrome: cytogenetic and molecular studies.
    Spinner NB, Rand EB, Fortina P, Genin A, Taub R, Semeraro A, Piccoli DA.
    Am J Hum Genet; 1994 Aug 01; 55(2):238-43. PubMed ID: 8037203
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  • 38. Alagille syndrome with prominent skin manifestations.
    Sengupta S, Das JK, Gangopadhyay A.
    Indian J Dermatol Venereol Leprol; 2005 Aug 01; 71(2):119-21. PubMed ID: 16394388
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