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157 related items for PubMed ID: 17157360

  • 21. Optimization of a simple and rapid single-strand conformation analysis for detection of mutations in the PROS1 gene: identification of seven novel mutations and three novel, apparently neutral, variants.
    Espinosa-Parrilla Y, Morell M, Borrell M, Souto JC, Fontcuberta J, Estivill X, Sala N.
    Hum Mutat; 2000; 15(5):463-73. PubMed ID: 10790208
    [Abstract] [Full Text] [Related]

  • 22. 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
    [Abstract] [Full Text] [Related]

  • 23. Association between estrogen receptor alpha and beta gene polymorphisms and deep vein thrombosis.
    Aléssio AM, Höehr NF, Siqueira LH, Ozelo MC, de Pádua Mansur A, Annichino-Bizzacchi JM.
    Thromb Res; 2007 Oct; 120(5):639-45. PubMed ID: 17184825
    [Abstract] [Full Text] [Related]

  • 24. 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
    [Abstract] [Full Text] [Related]

  • 25. Inherited thrombophilia and first venous thromboembolism during pregnancy and puerperium.
    Martinelli I, De Stefano V, Taioli E, Paciaroni K, Rossi E, Mannucci PM.
    Thromb Haemost; 2002 May; 87(5):791-5. PubMed ID: 12038778
    [Abstract] [Full Text] [Related]

  • 26. Deficiencies of antithrombin, protein C and protein S - practical experience in genetic analysis of a large patient cohort.
    Caspers M, Pavlova A, Driesen J, Harbrecht U, Klamroth R, Kadar J, Fischer R, Kemkes-Matthes B, Oldenburg J.
    Thromb Haemost; 2012 Aug; 108(2):247-57. PubMed ID: 22627591
    [Abstract] [Full Text] [Related]

  • 27. Two mutations in exon XII of the protein S alpha gene in four thrombophilic families resulting in premature stop codons and depressed levels of mutated mRNA.
    Andersen BD, Lind B, Philips M, Hansen AB, Ingerslev J, Thorsen S.
    Thromb Haemost; 1996 Aug; 76(2):143-50. PubMed ID: 8865520
    [Abstract] [Full Text] [Related]

  • 28. Risk of venous thrombosis in carriers of the prothrombin G20210A variant and factor V Leiden and their interaction with oral contraceptives.
    Aznar J, Vayá A, Estellés A, Mira Y, Seguí R, Villa P, Ferrando F, Falcó C, Corella D, España F.
    Haematologica; 2000 Dec; 85(12):1271-6. PubMed ID: 11114134
    [Abstract] [Full Text] [Related]

  • 29. [A novel gene mutation in a congenital protein S deficiency pedigree].
    Liu L, He L, Yang S.
    Zhonghua Xue Ye Xue Za Zhi; 2001 Sep; 22(9):457-60. PubMed ID: 11758223
    [Abstract] [Full Text] [Related]

  • 30. 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; 137(2):178-84. PubMed ID: 22261441
    [Abstract] [Full Text] [Related]

  • 31. Phenotypic APC resistance in carriers of the A20210 prothrombin mutation is associated with an increased risk of venous thrombosis.
    Castaman G, Tosetto A, Simioni M, Ruggeri M, Madeo D, Rodeghiero F.
    Thromb Haemost; 2001 Sep; 86(3):804-8. PubMed ID: 11583311
    [Abstract] [Full Text] [Related]

  • 32. Free protein S deficiency is a risk factor for venous thrombosis.
    Faioni EM, Valsecchi C, Palla A, Taioli E, Razzari C, Mannucci PM.
    Thromb Haemost; 1997 Nov; 78(5):1343-6. PubMed ID: 9408016
    [Abstract] [Full Text] [Related]

  • 33. Protein S deficiency: a clinical perspective.
    ten Kate MK, van der Meer J.
    Haemophilia; 2008 Nov; 14(6):1222-8. PubMed ID: 18479427
    [Abstract] [Full Text] [Related]

  • 34. The paradoxical association between inherited factor VII deficiency and venous thrombosis.
    Marty S, Barro C, Chatelain B, Fimbel B, Tribout B, Reynaud J, Schved JF, Giansily-Blaizot M.
    Haemophilia; 2008 May; 14(3):564-70. PubMed ID: 18282149
    [Abstract] [Full Text] [Related]

  • 35. Familial thrombophilia is an oligogenetic disease: involvement of the prothrombin G20210A, PROC and PROS gene mutations.
    Boinot C, Borgel D, Kitzis A, Guicheteau M, Aiach M, Alhenc-Gelas M.
    Blood Coagul Fibrinolysis; 2003 Feb; 14(2):191-6. PubMed ID: 12632031
    [Abstract] [Full Text] [Related]

  • 36. [Recurrent deep vein thrombosis caused by heterozygous missense mutation of the protein S gene: genetic analysis of a case].
    Ye X, Liu XL, Feng Y, Zhou XH, Xing ZF.
    Nan Fang Yi Ke Da Xue Xue Bao; 2011 Jun; 31(7):1228-31. PubMed ID: 21764702
    [Abstract] [Full Text] [Related]

  • 37. Poor relationship between phenotypes of protein S deficiency and mutations in the protein S alpha gene.
    Hermida J, Faioni EM, Mannucci PM.
    Thromb Haemost; 1999 Dec; 82(6):1634-8. PubMed ID: 10613647
    [Abstract] [Full Text] [Related]

  • 38. The HR2 haplotype of factor V: effects on factor V levels, normalized activated protein C sensitivity ratios and the risk of venous thrombosis.
    de Visser MC, Guasch JF, Kamphuisen PW, Vos HL, Rosendaal FR, Bertina RM.
    Thromb Haemost; 2000 Apr; 83(4):577-82. PubMed ID: 10780320
    [Abstract] [Full Text] [Related]

  • 39. Association of genotypes of thrombin-activatable fibrinolysis inhibitors with thrombotic microangiopathies--a pilot study.
    Sucker C, Hetzel GR, Farokhzad F, Dahhan F, Schmitz M, Kurschat C, Grabensee B, Maruhn-Debowski B, Zotz R, Scharf R.
    Nephrol Dial Transplant; 2007 May; 22(5):1347-50. PubMed ID: 17327284
    [Abstract] [Full Text] [Related]

  • 40. 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
    [Abstract] [Full Text] [Related]

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