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Journal Abstract Search

300 related items for PubMed ID: 35385937

  • 1. [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]

  • 2. [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
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  • 3. Familial screening of children with Wilson disease: Necessity of screening in previous generation and screening methods.
    Li H, Liu L, Li Y, He S, Liu Y, Li J, Tao R, Li W, Shang S.
    Medicine (Baltimore); 2018 Jul 20; 97(27):e11405. PubMed ID: 29979436
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  • 4. 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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  • 8. 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 12; 48(5):102335. PubMed ID: 38588792
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  • 10. Contribution of intragenic deletions to mutation spectrum in Chinese patients with Wilson's disease and possible mechanism underlying ATP7B gross deletions.
    Chen YC, Yu H, Wang RM, Xie JJ, Ni W, Zhang Y, Dong Y, Wu ZY.
    Parkinsonism Relat Disord; 2019 May 12; 62():128-133. PubMed ID: 30655162
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  • 11. 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
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  • 12. Clinical characteristics and prognosis of early diagnosed Wilson's disease: A large cohort study.
    Li S, Lin Y, Chen S, Zhang W, Chen YM, Lu X, Shao Y, Lu Z, Sheng H, Guan Z, Zheng R, Liang C, Chen Y, Liu L, Zeng C.
    Liver Int; 2024 Sep 01; 44(9):2424-2433. PubMed ID: 38847512
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  • 14. 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 01; 19(3):590-596. PubMed ID: 32485301
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  • 16. [Wilson disease: an update].
    Seo JK.
    Korean J Hepatol; 2006 Sep 01; 12(3):333-63. PubMed ID: 16998287
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  • 17. Mutational analysis of exon 8 and exon 14 of ATP7B gene in Bangladeshi children with Wilson disease.
    Tasmeen R, Karim ASMB, Banu LA, Hossain E, Rokunuzzaman M, Majumder W, Alam ST, Rasid R, Benzamin M, Hasan MS.
    Indian J Gastroenterol; 2022 Oct 01; 41(5):456-464. PubMed ID: 36308701
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  • 18. A novel gross deletion and breakpoint junction sequence analysis of ATP7B in a Chinese family with Wilson disease using next‑generation sequencing and Sanger sequencing.
    Liu WL, Li F, Liu L, Chen W, He ZX, Gu H, Ai R.
    Mol Med Rep; 2020 Jan 01; 21(1):517-523. PubMed ID: 31746411
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