These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
254 related articles for article (PubMed ID: 18435454)
21. Association of protein S p.Pro667Pro dimorphism with plasma protein S levels in normal individuals and patients with inherited protein S deficiency. Castaman G; Biguzzi E; Razzari C; Tosetto A; Fontana G; Asti D; Brancaccio V; Castori D; Lane DA; Faioni EM; Thromb Res; 2007; 120(3):421-6. PubMed ID: 17157360 [TBL] [Abstract][Full Text] [Related]
22. Absence of linkage between type III protein S deficiency and the PROS1 and C4BP genes in families carrying the protein S Heerlen allele. Espinosa-Parrilla Y; Morell M; Souto JC; Borrell M; Heine-Suñer D; Tirado I; Volpini V; Estivill X; Sala N Blood; 1997 Apr; 89(8):2799-806. PubMed ID: 9108398 [TBL] [Abstract][Full Text] [Related]
23. 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 [TBL] [Abstract][Full Text] [Related]
24. Characterization and structural impact of five novel PROS1 mutations in eleven protein S-deficient families. Andersen BD; Bisgaard ML; Lind B; Philips M; Villoutreix B; Thorsen S Thromb Haemost; 2001 Dec; 86(6):1392-9. PubMed ID: 11776305 [TBL] [Abstract][Full Text] [Related]
25. [Molecular mechanisms of recurrent venous thrombosis in two pedigrees with type I antithrombin deficiency]. Xia Y; Ding QL; Xu GQ; Zhang LW; Dai J; Lu YL; Wang XF; Xi XD; Wang HL Zhonghua Xue Ye Xue Za Zhi; 2011 Dec; 32(12):848-53. PubMed ID: 22339960 [TBL] [Abstract][Full Text] [Related]
26. Protein C and protein S deficiency - practical diagnostic issues. Wypasek E; Undas A Adv Clin Exp Med; 2013; 22(4):459-67. PubMed ID: 23986205 [TBL] [Abstract][Full Text] [Related]
27. 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 [TBL] [Abstract][Full Text] [Related]
28. 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 [TBL] [Abstract][Full Text] [Related]
29. Functional characterization of twelve natural PROS1 mutations associated with anticoagulant protein S deficiency. Hurtado B; Muñoz X; Mulero MC; Navarro G; Domènech P; García de Frutos P; Pérez-Riba M; Sala N Haematologica; 2008 Apr; 93(4):574-80. PubMed ID: 18322254 [TBL] [Abstract][Full Text] [Related]
30. 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; ():. PubMed ID: 20378562 [TBL] [Abstract][Full Text] [Related]
31. 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 [TBL] [Abstract][Full Text] [Related]
32. Molecular mechanisms of antithrombin deficiency in two Chinese families. One novel and one recurrent point mutation in the antithrombin gene causing venous thrombosis. Zhou RF; Fu QH; Wang WB; Xie S; Dai J; Ding QL; Wang XF; Wang HL; Wang ZY Thromb Haemost; 2005 Dec; 94(6):1172-6. PubMed ID: 16411389 [TBL] [Abstract][Full Text] [Related]
33. Protein C and protein S assessment in hospital laboratories: which strategy and what role for DNA sequencing? Labrouche S; Reboul MP; Guérin V; Vergnes C; Freyburger G Blood Coagul Fibrinolysis; 2003 Sep; 14(6):531-8. PubMed ID: 12960605 [TBL] [Abstract][Full Text] [Related]
34. Identification of three novel mutations in hereditary protein S deficiency. Bustorff TC; Freire I; Gago T; Crespo F; David D Thromb Haemost; 1997 Jan; 77(1):21-5. PubMed ID: 9031443 [TBL] [Abstract][Full Text] [Related]
35. 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 [TBL] [Abstract][Full Text] [Related]
36. Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. Biguzzi E; Razzari C; Lane DA; Castaman G; Cappellari A; Bucciarelli P; Fontana G; Margaglione M; D'Andrea G; Simmonds RE; Rezende SM; Preston R; Prisco D; Faioni EM; Hum Mutat; 2005 Mar; 25(3):259-69. PubMed ID: 15712227 [TBL] [Abstract][Full Text] [Related]
37. A mutation in the protein S pseudogene is linked to protein S deficiency in a thrombophilic family. Ploos van Amstel HK; Reitsma PH; Hamulyák K; de Die-Smulders CE; Mannucci PM; Bertina RM Thromb Haemost; 1989 Nov; 62(3):897-901. PubMed ID: 2531940 [TBL] [Abstract][Full Text] [Related]
38. 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 [TBL] [Abstract][Full Text] [Related]
39. Low cut-off values increase diagnostic performance of protein S assays. Mulder R; Ten Kate MK; Kluin-Nelemans HC; Mulder AB Thromb Haemost; 2010 Sep; 104(3):618-25. PubMed ID: 20539904 [TBL] [Abstract][Full Text] [Related]
40. The prevalence of, and molecular defects underlying, inherited protein S deficiency in the general population. Beauchamp NJ; Dykes AC; Parikh N; Campbell Tait R; Daly ME Br J Haematol; 2004 Jun; 125(5):647-54. PubMed ID: 15147381 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]