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Journal Abstract Search

229 related items for PubMed ID: 24507871

  • 1. PROS1 mutations associated with protein S deficiency in Polish patients with residual vein obstruction on rivaroxaban therapy.
    Wypasek E, Potaczek DP, Alhenc-Gelas M, Undas A.
    Thromb Res; 2014 Jul; 134(1):199-201. PubMed ID: 24507871
    [No Abstract] [Full Text] [Related]

  • 2. Protein S deficiency and novel oral anticoagulants: an intriguing case.
    Tàssies D, García de Frutos P.
    Thromb Res; 2014 Jul; 134(1):1-2. PubMed ID: 24642006
    [No Abstract] [Full Text] [Related]

  • 3. 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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  • 4. 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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  • 6. 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; 98(4):783-9. PubMed ID: 17938802
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  • 8. 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; 90(4):537-539. PubMed ID: 19826897
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  • 9. First case of protein S deficiency due to a translocation t(3;21)(q11.2;q22).
    Hurtado B, Nadal M, Margarit E, Sánchez A, Abasolo N, García N, Doménech P, Sala N.
    Thromb Haemost; 2009 May; 101(5):977-9. PubMed ID: 19404554
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  • 15. Clinical characteristics, genes identification and follow-up study of a patient with central venous thrombosis from a protein S deficiency pedigree.
    Wang T, Zhao XJ, Zhu HD, Lu M, Wen B, Ma L.
    Eur Rev Med Pharmacol Sci; 2021 Jan; 25(1):353-361. PubMed ID: 33506924
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  • 17. Severe arterial thrombosis in a family with type III protein S deficiency caused by a frameshift mutation in the PROS1 gene.
    Larsen TB, Brusgaard K, Nybo M.
    Thromb Res; 2010 Aug; 126(2):e159-61. PubMed ID: 20398916
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  • 19. 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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  • 20. Genetic characterization of antithrombin, protein C, and protein S deficiencies in Polish patients.
    Wypasek E, Corral J, Alhenc-Gelas M, Sydor W, Iwaniec T, Celińska-Lowenhoff M, Potaczek DP, Blecharczyk A, Zawilska K, Musiał J, Undas A.
    Pol Arch Intern Med; 2017 Aug 09; 127(7-8):512-523. PubMed ID: 28607330
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