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Journal Abstract Search

153 related items for PubMed ID: 38588792

  • 1. Phenotype and molecular characterization of Wilson's disease in Morocco.
    Abbassi N, Bourrahouat A, Bedoya EC, Pagan C, Qabli ME, Maidoumi S, Belmalih A, Guillaud O, Kissani N, Abkari A, Chahid I, Rafai MA, Mouane N, Kriouile Y, Aidi S, Hida M, Idrissi ML, Belahsen MF, Abkari ME, Rkain M, Ismaili Z, Sedki A, Bost M, Aboussair N, Lachaux A.
    Clin Res Hepatol Gastroenterol; 2024 May; 48(5):102335. PubMed ID: 38588792
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  • 2. [Phenotypes and ATP7B gene variants in 316 children with Wilson disease].
    Lu ZK, Cheng J, Li SM, Lin YT, Zhang W, Li XZ, Sheng HY, Mao XJ, Mei HF, Zheng RD, Liang CL, Jiang MY, Huang YL, Liu L, Zeng CH.
    Zhonghua Er Ke Za Zhi; 2022 Apr 02; 60(4):317-322. PubMed ID: 35385937
    [Abstract] [Full Text] [Related]

  • 3. Epidemiology, clinical features, and mortality rate of Wilson disease in Moroccan children: A pediatric case series.
    Abbassi N, Bourrahouat A, Bedoya EC, Belmalih A, El Hanafi FZ, Bost M, Sedki A, Lachaux A.
    Arch Pediatr; 2022 Aug 02; 29(6):453-458. PubMed ID: 35705388
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  • 5. ATP7B mutations in families in a predominantly Southern Indian cohort of Wilson's disease patients.
    Santhosh S, Shaji RV, Eapen CE, Jayanthi V, Malathi S, Chandy M, Stanley M, Selvi S, Kurian G, Chandy GM.
    Indian J Gastroenterol; 2006 Aug 02; 25(6):277-82. PubMed ID: 17264425
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  • 6. Genetic and Clinical Analysis in a Cohort of Patients with Wilson's Disease in Southwestern China.
    Liu Y, Zhou H, Guo H, Bai Y.
    Arch Med Res; 2015 Feb 02; 46(2):164-9. PubMed ID: 25704634
    [Abstract] [Full Text] [Related]

  • 7. Whole-exome sequencing identifies novel pathogenic variants across the ATP7B gene and some modifiers of Wilson's disease phenotype.
    Kluska A, Kulecka M, Litwin T, Dziezyc K, Balabas A, Piatkowska M, Paziewska A, Dabrowska M, Mikula M, Kaminska D, Wiernicka A, Socha P, Czlonkowska A, Ostrowski J.
    Liver Int; 2019 Jan 02; 39(1):177-186. PubMed ID: 30230192
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  • 9. Phenotypic and genetic characterization of children with Wilson Disease from Northeast China.
    Zhang T, Song W, Mao Z.
    BMC Pediatr; 2024 Sep 12; 24(1):576. PubMed ID: 39267050
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  • 10. [Phenotype and genotype analysis of 55 children patients with Wilson's disease].
    Zhou XY, Yin HX, Wang CL, Liu ZF, Zheng BX, Jin Y.
    Zhonghua Gan Zang Bing Za Zhi; 2020 Jul 20; 28(7):603-607. PubMed ID: 32791797
    [Abstract] [Full Text] [Related]

  • 11. Clinical presentation, diagnosis and long-term outcome of Wilson's disease: a cohort study.
    Merle U, Schaefer M, Ferenci P, Stremmel W.
    Gut; 2007 Jan 20; 56(1):115-20. PubMed ID: 16709660
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  • 12. [Wilson disease: an update].
    Seo JK.
    Korean J Hepatol; 2006 Sep 20; 12(3):333-63. PubMed ID: 16998287
    [Abstract] [Full Text] [Related]

  • 13. Mutation analysis of the ATP7B gene and genotype-phenotype correlation in Chinese patients with Wilson disease.
    Li M, Ma J, Wang W, Yang X, Luo K.
    BMC Gastroenterol; 2021 Sep 01; 21(1):339. PubMed ID: 34470610
    [Abstract] [Full Text] [Related]

  • 14. Genotype phenotype correlation in Wilson's disease within families--a report on four south Indian families.
    Santhosh S, Shaji RV, Eapen CE, Jayanthi V, Malathi S, Finny P, Thomas N, Chandy M, Kurian G, Chandy GM.
    World J Gastroenterol; 2008 Aug 07; 14(29):4672-6. PubMed ID: 18698682
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  • 18. Role for Biochemical Assays and Kayser-Fleischer Rings in Diagnosis of Wilson's Disease.
    Dong Y, Wang RM, Yang GM, Yu H, Xu WQ, Xie JJ, Zhang Y, Chen YC, Ni W, Wu ZY.
    Clin Gastroenterol Hepatol; 2021 Mar 07; 19(3):590-596. PubMed ID: 32485301
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  • 20. Wilson's disease in Lebanon and regional countries: Homozygosity and hepatic phenotype predominance.
    Barada K, El Haddad A, Katerji M, Jomaa M, Usta J.
    World J Gastroenterol; 2017 Sep 28; 23(36):6715-6725. PubMed ID: 29085216
    [Abstract] [Full Text] [Related]

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