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PUBMED FOR HANDHELDS

Journal Abstract Search


139 related items for PubMed ID: 28734329

  • 1. Leptochoroid in a Case of Alagille Syndrome (Arteriohepatic Dysplasia).
    Shen JH, Chen KJ, Wang NK.
    Ophthalmology; 2017 Aug; 124(8):1135. PubMed ID: 28734329
    [No Abstract] [Full Text] [Related]

  • 2. Macular atrophy and focal choroidal excavation in a patient with JAG1- related alagille syndrome.
    Ruiz-Chavolla D, Barragán-Arévalo T, Cortes-Muñoz D, Sánchez-Ruiz J, Zenteno JC, Ledesma-Gil G.
    Ophthalmic Genet; 2024 Jun; 45(3):299-302. PubMed ID: 38526149
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  • 3. An Atypical Presentation of Alagille Syndrome.
    Wu KY, Treece AL, Russo PA, Wen JW.
    Pediatr Dev Pathol; 2018 Jun; 21(1):79-83. PubMed ID: 29187043
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  • 6. Alagille Syndrome.
    Mitchell E, Gilbert M, Loomes KM.
    Clin Liver Dis; 2018 Nov; 22(4):625-641. PubMed ID: 30266153
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  • 9. Alagille syndrome with atypical phenotype diagnosed by molecular tests: unreported JAG1 mutation.
    Marín Urueña SI, Montejo Vicente MM, Garrote Adrados JA.
    Med Clin (Barc); 2017 Nov 22; 149(10):462. PubMed ID: 28648591
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  • 12. A novel JAG1 frameshift variant causing Alagille syndrome with incomplete penetrance.
    Yang Y, Wang H.
    Clin Biochem; 2022 Jun 22; 104():19-21. PubMed ID: 35151641
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  • 18. CHORIORETINAL ATROPHY IN ALAGILLE SYNDROME.
    Esmaili DD.
    Retin Cases Brief Rep; 2015 Jun 22; 9(4):330-2. PubMed ID: 26355821
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  • 19. Middle aortic syndrome in a boy with arteriohepatic dysplasia (Alagille syndrome).
    Shefler AG, Chan MK, Ostman-Smith I.
    Pediatr Cardiol; 1997 Jun 22; 18(3):232-4. PubMed ID: 9142719
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  • 20. A novel JAG1 mutation causing Alagille syndrome presenting with giant hepatic nodules and discordant phenotype in monozygotic twins.
    Zhang Y, Xiang B, Yu X.
    Med Clin (Barc); 2020 Dec 11; 155(11):507-509. PubMed ID: 31522744
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