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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

92 related articles for article (PubMed ID: 7580547)

  • 1. Survival in families with hereditary protein C deficiency, 1820 to 1993.
    Allaart CF; Rosendaal FR; Noteboom WM; Vandenbroucke JP; Briët E
    BMJ; 1995 Oct; 311(7010):910-3. PubMed ID: 7580547
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Increased risk of venous thrombosis in carriers of hereditary protein C deficiency defect.
    Allaart CF; Poort SR; Rosendaal FR; Reitsma PH; Bertina RM; Briët E
    Lancet; 1993 Jan; 341(8838):134-8. PubMed ID: 8093743
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effects.
    Reitsma PH; Poort SR; Allaart CF; Briët E; Bertina RM
    Blood; 1991 Aug; 78(4):890-4. PubMed ID: 1868249
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The significance of F139V mutation on thrombotic events in compound heterozygous and homozygous protein C deficiency.
    Yang LH; Zheng FX; Chen Y; Jin YH; Zhang Z; Xie HX; Yang XL; Wang MS; Chen BC
    Blood Coagul Fibrinolysis; 2014 Dec; 25(8):824-30. PubMed ID: 24911457
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Application of two neutral MspI DNA polymorphisms in the analysis of hereditary protein C deficiency.
    Reitsma PH; te Lintel Hekkert W; Koenhen E; van der Velden PA; Allaart CF; Deutz-Terlouw PP; Poort SR; Bertina RM
    Thromb Haemost; 1990 Oct; 64(2):239-44. PubMed ID: 1702905
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Gene mutations in 21 unrelated cases of phenotypic heterozygous protein C deficiency and thrombosis. Protein C Study Group.
    Ireland H; Thompson E; Lane DA
    Thromb Haemost; 1996 Dec; 76(6):867-73. PubMed ID: 8972002
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of 58 Mutations (26 Novel) in 94 of 109 Symptomatic Spanish Probands with Protein C Deficiency.
    Martos L; Fernández-Pardo Á; López-Fernández MF; Ibáñez F; Herrero S; Tàssies D; González-Porras JR; Solmoirago MJ; Costa MJ; Reverter JC; Marco P; Roldán V; Lecumberri R; Velasco F; Oto J; Iruin G; Alonso MN; Vayá A; Bonanad S; Ferrando F; Martí E; Cid AR; Plana E; Oña F; Cuesta I; González-López TJ; España F; Medina P; Navarro S;
    Thromb Haemost; 2019 Sep; 119(9):1409-1418. PubMed ID: 31254973
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hereditary deficiency of protein C or protein S confers increased risk of arterial thromboembolic events at a young age: results from a large family cohort study.
    Mahmoodi BK; Brouwer JL; Veeger NJ; van der Meer J
    Circulation; 2008 Oct; 118(16):1659-67. PubMed ID: 18824642
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Analysis of phenotypes and genetic mutations in two pedigrees affected with hereditary protein C deficiency].
    Yang L; Jin Y; Yang T; Chen X; Zhu L; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):10-14. PubMed ID: 28186585
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 95(4):294-307. PubMed ID: 25533856
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis.
    Tjeldhorn L; Sandset PM; Haugbro K; Skretting G
    Thromb Res; 2010 Mar; 125(3):230-4. PubMed ID: 19535131
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hereditary antithrombin deficiency: heterogeneity of the molecular basis and mortality in Dutch families.
    van Boven HH; Olds RJ; Thein SL; Reitsma PH; Lane DA; Briët E; Vandenbroucke JP; Rosendaal FR
    Blood; 1994 Dec; 84(12):4209-13. PubMed ID: 7994035
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary homozygous heparin cofactor II deficiency and the risk of developing venous thrombosis.
    Villa P; Aznar J; Vaya A; España F; Ferrando F; Mira Y; Estellés A
    Thromb Haemost; 1999 Sep; 82(3):1011-4. PubMed ID: 10494755
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Compound heterozygosity in a family with protein C deficiency illustrating the complexity of the underlying molecular mechanism.
    Gandrille S; Jude B; Alhenc-Gelas M; Millaire A; Aiach M
    Thromb Haemost; 1993 Nov; 70(5):747-52. PubMed ID: 8128429
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An unknown genetic defect increases venous thrombosis risk, through interaction with protein C deficiency.
    Hasstedt SJ; Bovill EG; Callas PW; Long GL
    Am J Hum Genet; 1998 Aug; 63(2):569-76. PubMed ID: 9683579
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mortality in hereditary antithrombin-III deficiency--1830 to 1989.
    Rosendaal FR; Heijboer H; Briët E; Büller HR; Brandjes DP; de Bruin K; Hommes DW; Vandenbroucke JP
    Lancet; 1991 Feb; 337(8736):260-2. PubMed ID: 1671110
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Biochemical activity and gene analysis of inherited protein C and antithrombin deficiency in two Chinese pedigrees.
    Zhou RF; Fu QH; Wang WB; Xie S; Hu YQ; Wang XF; Wang ZY; Wang HL
    Chin Med J (Engl); 2004 Jun; 117(6):813-7. PubMed ID: 15198878
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Different impact of two mutations of a novel compound heterozygous protein C deficiency with late onset thrombosis.
    Yang LH; Wang MS; Zheng FX; Li J; Chen Y; Jin YH; Xie HX; Yang XL; Chen BC
    Genet Mol Res; 2014 Apr; 13(2):2969-77. PubMed ID: 24782131
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Analysis of an hereditary protein C deficiency pedigree with compound heterozygous gene mutations].
    Yang LH; Zhu LQ; Yang XO; Wang MS; Li J; Chen BC; Jin YH; Zhang Z; Zheng FX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Oct; 29(5):515-8. PubMed ID: 23042384
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dysfunctional protein C deficiency (type II). A report of 11 cases in 3 American families and review of the literature.
    Berdeaux DH; Abshire TC; Marlar RA
    Am J Clin Pathol; 1993 Jun; 99(6):677-86. PubMed ID: 8322701
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.