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Journal Abstract Search

152 related items for PubMed ID: 37950050

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  • 4. Genetic background analysis of protein C deficiency demonstrates a recurrent mutation associated with venous thrombosis in Chinese population.
    Tang L, Guo T, Yang R, Mei H, Wang H, Lu X, Yu J, Wang Q, Hu Y.
    PLoS One; 2012; 7(4):e35773. PubMed ID: 22545135
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  • 5. Two heterozygous mutations associated with type I protein C deficiency in two Chinese independent families.
    Xu Q, Wang M, Jin Y, Liu S, Luo S, Yang L.
    Blood Coagul Fibrinolysis; 2021 Dec 01; 32(8):596-602. PubMed ID: 34261859
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  • 7. The clinical presentation and genotype of protein C deficiency with double mutations of the protein C gene.
    Inoue H, Terachi SI, Uchiumi T, Sato T, Urata M, Ishimura M, Koga Y, Hotta T, Hara T, Kang D, Ohga S.
    Pediatr Blood Cancer; 2017 Jul 01; 64(7):. PubMed ID: 28111891
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  • 9. Severe Protein C Deficiency due to Novel Biallelic Variants in PROC and Their Phenotype Correlation.
    Barg AA, Dardik R, Levin C, Koren A, Levy-Mendelovich S, Pode-Shakked B, Kenet G.
    Acta Haematol; 2021 Jul 01; 144(3):327-331. PubMed ID: 32980846
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  • 10. Familial thrombotic risk based on the genetic background of Protein C Deficiency in a Portuguese Study.
    Fidalgo T, Martinho P, Salvado R, Manco L, Oliveira AC, Pinto CS, Gonçalves E, Marques D, Sevivas T, Martins N, Ribeiro ML.
    Eur J Haematol; 2015 Oct 01; 95(4):294-307. PubMed ID: 25533856
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  • 12. Protein C deficiency as the major cause of thrombophilias in childhood.
    Ohga S, Ishiguro A, Takahashi Y, Shima M, Taki M, Kaneko M, Fukushima K, Kang D, Hara T, Japan Childhood Thrombophilia Study Group.
    Pediatr Int; 2013 Jun 01; 55(3):267-71. PubMed ID: 23521084
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  • 13. Identification of mutations in 15 Hungarian families with hereditary protein C deficiency.
    Dávid M, Losonczy H, Sas G, Nagy A, Kutscher G, Meyer M.
    Br J Haematol; 2000 Oct 01; 111(1):129-35. PubMed ID: 11091192
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  • 17. Pathogenic variants of PROC gene caused type II activity deficiency in a Chinese family: A case report.
    Zhu H, Liu H, Liu J.
    Medicine (Baltimore); 2021 Mar 26; 100(12):e25160. PubMed ID: 33761690
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  • 19. R147W mutation of PROC gene is common in venous thrombotic patients in Taiwanese Chinese.
    Tsay W, Shen MC.
    Am J Hematol; 2004 May 26; 76(1):8-13. PubMed ID: 15114590
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