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Journal Abstract Search

175 related items for PubMed ID: 29742732

  • 1. Recurrent pulmonary embolism associated with deep venous thrombosis diagnosed as protein s deficiency owing to a novel mutation in PROS1: A case report.
    Huang X, Xu F, Assa CR, Shen L, Chen B, Liu Z.
    Medicine (Baltimore); 2018 May; 97(19):e0714. PubMed ID: 29742732
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  • 2. One novel and one recurrent mutation in the PROS1 gene cause type I protein S deficiency in patients with pulmonary embolism associated with deep vein thrombosis.
    Mizukami K, Nakabayashi T, Naitoh S, Takeda M, Tarumi T, Mizoguchi I, Ieko M, Koike T.
    Am J Hematol; 2006 Oct; 81(10):787-97. PubMed ID: 16868938
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  • 3. A novel nonsense mutation Tyr301* of PROS1 causing protein S deficiency.
    Jang MA, Kim SH, Kim DK, Kim HJ.
    Blood Coagul Fibrinolysis; 2015 Mar; 26(2):223-4. PubMed ID: 25255242
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  • 4. Clinical Manifestation and Mutation Spectrum of 53 Unrelated Pedigrees with Protein S Deficiency in China.
    Li L, Wu X, Wu W, Ding Q, Cai X, Wang X.
    Thromb Haemost; 2019 Mar; 119(3):449-460. PubMed ID: 30669159
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  • 5. Compound heterozygous mutations identified in severe type I protein S deficiency impaired the secretion of protein S.
    Zhou J, Shen W, Gu Y, Li M, Shen W.
    J Clin Pathol; 2020 Jan; 73(1):7-13. PubMed ID: 31422373
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  • 6. PROS1 variant c.1574C>T p.Ala525Val causes portal vein thrombosis with protein S deficiency.
    Ye X, Mi X, Sun J, ShenTu Y, Fei Y, Tang D, Ye X, Ma X, Shi J, Chen G, Gong L.
    Clin Res Hepatol Gastroenterol; 2023 May; 47(6):102141. PubMed ID: 37207893
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  • 9. A novel PROS1 mutation, c.74dupA, was identified in a protein S deficiency family.
    Zhang Y, Yang H, Chen Q, Yu J, Chen X, Liu S, Gao G, Song Y, Zhou Z.
    Thromb Res; 2016 Dec; 148():125-127. PubMed ID: 27846449
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  • 10. A rare splicing mutation in the PROS1 gene of a Korean patient with type I hereditary protein S deficiency.
    Choi J, Kim HJ, Chang MH, Choi JR, Yoo JH.
    Ann Clin Lab Sci; 2011 Dec; 41(4):397-400. PubMed ID: 22166512
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  • 11. Venous thromboembolism associated with protein S deficiency due to Arg451* mutation in PROS1 gene: a case report and a literature review.
    Wypasek E, Karpinski M, Alhenc-Gelas M, Undas A.
    J Genet; 2017 Dec; 96(6):1047-1051. PubMed ID: 29321366
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  • 16. Protein S deficiency with a PROS1 gene mutation in a patient presenting with mesenteric venous thrombosis following total colectomy.
    Ji M, Yoon SN, Lee W, Jang S, Park SH, Kim DY, Chun S, Min WK.
    Blood Coagul Fibrinolysis; 2011 Oct; 22(7):619-21. PubMed ID: 21799399
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  • 17. PROS1 genotype phenotype relationships in a large cohort of adults with suspicion of inherited quantitative protein S deficiency.
    Alhenc-Gelas M, Plu-Bureau G, Horellou MH, Rauch A, Suchon P, GEHT genetic thrombophilia group.
    Thromb Haemost; 2016 Mar; 115(3):570-9. PubMed ID: 26466767
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  • 18. Lessons from an elderly patient with pulmonary embolism caused by protein S deficiency: a case report.
    Qiang L, Hong L, Min S, Hongping W, Xian C, Tianlang L.
    J Med Case Rep; 2024 Feb 28; 18(1):77. PubMed ID: 38414076
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  • 20. Compound heterozygous mutations in the PROS1 gene responsible for quantitative and qualitative protein S deficiency.
    Yamanouchi J, Hato T, Tamura T, Fujiwara H, Yakushijin Y, Yasukawa M.
    Int J Hematol; 2009 Nov 28; 90(4):537-539. PubMed ID: 19826897
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