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Journal Abstract Search

207 related items for PubMed ID: 21799399

  • 1. 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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  • 4. 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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  • 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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  • 7. Mesenteric venous thrombosis in a child with type 2 protein S deficiency.
    Hayakawa T, Morimoto A, Nozaki Y, Kashii Y, Aihara T, Maeda K, Momoi MY.
    J Pediatr Hematol Oncol; 2011 Mar; 33(2):141-3. PubMed ID: 21285903
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  • 8. Similar hypercoagulable state and thrombosis risk in type I and type III protein S-deficient individuals from mixed type I/III families.
    Castoldi E, Maurissen LF, Tormene D, Spiezia L, Gavasso S, Radu C, Hackeng TM, Rosing J, Simioni P.
    Haematologica; 2010 Apr 07. PubMed ID: 20378562
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  • 9. Genotype and laboratory and clinical phenotypes of protein s deficiency.
    Duebgen S, Kauke T, Marschall C, Giebl A, Lison S, Hart C, Dick A, Spannagl M.
    Am J Clin Pathol; 2012 Feb 07; 137(2):178-84. PubMed ID: 22261441
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  • 10. 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 07; 115(3):570-9. PubMed ID: 26466767
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  • 16. Heerlen polymorphism associated with type III protein S deficiency and factor V Leiden mutation in a Polish patient with deep vein thrombosis.
    Wypasek E, Potaczek DP, Alhenc-Gelas M, Undas A.
    Blood Coagul Fibrinolysis; 2014 Jan 07; 25(1):84-5. PubMed ID: 24365770
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  • 17. Inherited protein S deficiency as a result of a large duplication mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification.
    Choung HS, Kim HJ, Gwak GY, Kim SH, Kim DK.
    J Thromb Haemost; 2008 Aug 07; 6(8):1430-2. PubMed ID: 18489710
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  • 18. A large deletion of the PROS1 gene in a deep vein thrombosis patient with protein S deficiency.
    Yin T, Takeshita S, Sato Y, Sakata T, Shin Y, Honda S, Kawasaki T, Tsuji H, Kojima T, Madoiwa S, Sakata Y, Murata M, Ikeda Y, Miyata T.
    Thromb Haemost; 2007 Oct 07; 98(4):783-9. PubMed ID: 17938802
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  • 20. Thrombophilia: disorders predisposing to venous thromboembolism.
    Pineo GF, Hull RD.
    Baillieres Clin Haematol; 1998 Sep 07; 11(3):525-40. PubMed ID: 10331092
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