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 *

111 related articles for article (PubMed ID: 18852482)

  • 1. True congenital prothrombin deficiency due to a 'new' mutation in the pre-propeptide (ARG-39 GLN).
    Girolami A; Santarossa L; Scarparo P; Candeo N; Girolami B
    Acta Haematol; 2008; 120(2):82-6. PubMed ID: 18852482
    [No Abstract]   [Full Text] [Related]  

  • 2. The hereditary transmission of congenital 'true' hypoprothrombinaemia.
    Girolami A
    Br J Haematol; 1971 Dec; 21(6):695-703. PubMed ID: 5132950
    [No Abstract]   [Full Text] [Related]  

  • 3. Prothrombin Suresnes: a case of homozygous F299V mutation responsible for hypodysprothrombinemia.
    François D; Chevreaud C; Vignon D; de Mazancourt P
    Haematologica; 2006 Mar; 91(3):431-2. PubMed ID: 16503555
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A natural variant with a point mutation resulting in a homozygous Arg to His substitution at position 388 in prothrombin.
    d'Audigier C; Pasmant E; Bournier O; Laurian Y; Guillin MC; Bezeaud A
    Haematologica; 2008 May; 93(5):799-800. PubMed ID: 18450742
    [No Abstract]   [Full Text] [Related]  

  • 5. Prothrombin deficiency caused by compound heterozygosity for two novel mutations in the prothrombin gene associated with a bleeding tendency.
    Stanchev H; Philips M; Villoutreix BO; Aksglaede L; Lethagen S; Thorsen S
    Thromb Haemost; 2006 Jan; 95(1):195-8. PubMed ID: 16543981
    [No Abstract]   [Full Text] [Related]  

  • 6. Homozygosity for a novel missense mutation in the prothrombin gene causing a severe bleeding disorder.
    Poort SR; Michiels JJ; Reitsma PH; Bertina RM
    Thromb Haemost; 1994 Dec; 72(6):819-24. PubMed ID: 7740448
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Abnormalities of prothrombin: a review of the pathophysiology, diagnosis, and treatment.
    Meeks SL; Abshire TC
    Haemophilia; 2008 Nov; 14(6):1159-63. PubMed ID: 19141155
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A common mutation, Arg457-->Gln, links prothrombin deficiencies in the Puerto Rican population.
    Lefkowitz JB; Weller A; Nuss R; Santiago-Borrero PJ; Brown DL; Ortiz IR
    J Thromb Haemost; 2003 Nov; 1(11):2381-8. PubMed ID: 14629473
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two novel mutations in the prothrombin gene identified in a patient with compound heterozygous type 1/2 prothrombin deficiency.
    Kuijper PH; Schellings MW; van de Kerkhof D; Nicolaes GA; Reitsma P; Halbertsma F; Dors N
    Haemophilia; 2013 Sep; 19(5):e304-6. PubMed ID: 23711336
    [No Abstract]   [Full Text] [Related]  

  • 10. Congenital prothrombin deficiency.
    Lancellotti S; De Cristofaro R
    Semin Thromb Hemost; 2009 Jun; 35(4):367-81. PubMed ID: 19598065
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation.
    Jayandharan G; Viswabandya A; Baidya S; Nair SC; Shaji RV; Chandy M; Srivastava A
    J Thromb Haemost; 2005 Jul; 3(7):1446-53. PubMed ID: 15892853
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Congenital deficiencies and abnormalities of prothrombin.
    Girolami A; Scarano L; Saggiorato G; Girolami B; Bertomoro A; Marchiori A
    Blood Coagul Fibrinolysis; 1998 Oct; 9(7):557-69. PubMed ID: 9863703
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A severe neonatal presentation of factor II deficiency.
    Pasmant E; Dumont B; Lacapere JJ; Dautzenberg MD; Bezeaud A
    Eur J Haematol; 2011 Nov; 87(5):464-6. PubMed ID: 21692854
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prophylactic administration of prothrombin complex concentrates for congenital prothrombin deficiency with a novel frameshift mutation, prothrombin saitama.
    Seki M; Koh K; Inoue T; Tomita Y; Kato M; Shimizu M; Morishita E; Hanada R
    Pediatr Blood Cancer; 2013 Mar; 60(3):503-5. PubMed ID: 23152198
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A second case of prothrombin Puerto Rico I in the United States.
    Kling SJ; Jones KA; Rodgers GM
    Am J Hematol; 2007 Jul; 82(7):661-2. PubMed ID: 17160994
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prothrombin Mumbai causes severe prothrombin deficiency due to a novel Cys90Ser mutation.
    Kulkarni B; Kanakia S; Ghosh K; Shetty S
    Ann Hematol; 2012 Oct; 91(10):1667-8. PubMed ID: 22392504
    [No Abstract]   [Full Text] [Related]  

  • 17. Two novel mutations in the prothrombin gene cause severe bleeding in a compound heterozygous patient.
    Poort SR; Njo KT; Vos HL; Bertina RM
    Blood Coagul Fibrinolysis; 1998 Nov; 9(8):761-4. PubMed ID: 9890721
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new variant of human prothrombin: prothrombin Metz, demonstration in a family showing double heterozygosity for congenital hypoprothrombinemia and dysprothrombinemia.
    Josso F; Rio Y; Béguin S
    Haemostasis; 1982; 12(4):309-16. PubMed ID: 7152370
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Analysis of phenotype and genotype in a Chinese pedigree with inherited prothrombin deficiency resulted from a homozygous mutation Tyr510Asp].
    Jin YH; Wang MS; Zheng FX
    Zhonghua Xue Ye Xue Za Zhi; 2012 Jul; 33(7):587-9. PubMed ID: 22967428
    [No Abstract]   [Full Text] [Related]  

  • 20. Prothrombin Saint-Denis: a natural variant with a point mutation resulting in Asp to Glu substitution at position 552 in prothrombin.
    Rouy S; Vidaud D; Alessandri JL; Dautzenberg MD; Venisse L; Guillin MC; Bezeaud A
    Br J Haematol; 2006 Mar; 132(6):770-3. PubMed ID: 16487178
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.