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 *

165 related articles for article (PubMed ID: 638074)

  • 1. Subunits A and S inheritance in four families with congenital factor XIII deficiency.
    Barbui T; Rodeghiero F; Dini E; Mariani G; Paa ML; De Biasi R; Murillo RC; Umana CM
    Br J Haematol; 1978 Feb; 38(2):267-71. PubMed ID: 638074
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Factor XIII deficiency. A family study by measurement of factor XIII subunits A and S.
    Francis JL; Todd PJ
    Acta Haematol; 1979; 62(3):167-72. PubMed ID: 118616
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new family with congenital factor XIII deficiency showing a deficit of both subunit A and B. Type I factor XIII deficiency.
    Capellato MG; Lazzaro AR; Marafioti F; Polato G; Girolami A
    Haematologia (Budap); 1987; 20(3):179-87. PubMed ID: 2891592
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Factor XIII levels in five families of patients with inherited factor XIII deficiency: support for an autosomal recessive inheritance.
    Fear JD; Miloszewski KJ; Losowsky MS
    Thromb Haemost; 1983 Aug; 50(2):588-90. PubMed ID: 6636036
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An electrophoretic and quantitative analysis of coagulation factor XIII in normal and deficient subjects.
    Board PG; Coggan M; Hamer JW
    Br J Haematol; 1980 Aug; 45(4):633-40. PubMed ID: 7426441
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital factor XIII deficiency. A family report.
    Thavaraj V; Singh Y; Choudhary VP; Saraya AK
    Haematologia (Budap); 1991; 24(2):107-11. PubMed ID: 1816054
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Subunit A of factor XIII regulates subunit B plasma concentration.
    Rodeghiero F; Morbin M; Barbui T
    Thromb Haemost; 1981 Oct; 46(3):621-2. PubMed ID: 7314056
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The normal and abnormal genes of the a and b subunits in coagulation factor XIII.
    Ichinose A; Izumi T; Hashiguchi T
    Semin Thromb Hemost; 1996; 22(5):385-91. PubMed ID: 8989821
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A familial factor XIII subunit B deficiency.
    Saito M; Asakura H; Yoshida T; Ito K; Okafuji K; Yoshida T; Matsuda T
    Br J Haematol; 1990 Mar; 74(3):290-4. PubMed ID: 2334637
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Electroimmunoassay of plasma subunits-a and -s in a case of congenital fibrin stabilizing factor deficiency.
    Barbui T; Cartei G; Chisesi T; Dini E
    Thromb Diath Haemorrh; 1974 Sep; 32(1):124-31. PubMed ID: 4454035
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Congenital deficiency of factor XIII caused by two missense mutations in a Dutch family.
    Onland W; Böing AN; Meijer AB; Schaap MC; Nieuwland R; Haasnoot K; Sturk A; Peters M
    Haemophilia; 2005 Sep; 11(5):539-47. PubMed ID: 16128900
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel and recurrent mutations in the F13A1 gene in unrelated Korean patients with congenital factor XIII deficiency.
    Jang MA; Park YS; Lee KO; Kim HJ
    Blood Coagul Fibrinolysis; 2015 Jan; 26(1):46-9. PubMed ID: 25004025
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.
    Borhany M; Handrkova H; Cairo A; Schroeder V; Fatima N; Naz A; Amanat S; Shamsi T; Peyvandi F; Kohler HP
    Haemophilia; 2014 Jul; 20(4):568-74. PubMed ID: 24329762
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fibrin cross-linking in congenital factor XIII deficiency.
    Rodeghiero F; Barbui T
    J Clin Pathol; 1980 May; 33(5):434-7. PubMed ID: 7400341
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Application of HUMF13A01 (AAAG)n STR polymorphism to the genetic diagnosis of coagulation factor XIII deficiency.
    Kangsadalampai S; Coggan M; Caglayan SH; Aktuglu G; Board PG
    Thromb Haemost; 1996 Dec; 76(6):879-82. PubMed ID: 8972004
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Factor XIII: congenital deficiency factor XIII, acquired deficiency, factor XIII A-subunit, and factor XIII B-subunit.
    Tahlan A; Ahluwalia J
    Arch Pathol Lab Med; 2014 Feb; 138(2):278-81. PubMed ID: 24476525
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines.
    Souri M; Biswas A; Misawa M; Omura H; Ichinose A
    Haemophilia; 2014 Mar; 20(2):255-62. PubMed ID: 24286209
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary factor XIII deficiency: report of four families and definition of the carrier state.
    Berliner S; Lusky A; Zivelin A; Modan M; Seligsohn U
    Br J Haematol; 1984 Mar; 56(3):495-505. PubMed ID: 6696852
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Tooth extraction in two patients who had a congenital deficiency of factor XIII.
    Suzuki H; Kaneda T
    J Oral Maxillofac Surg; 1985 Mar; 43(3):221-4. PubMed ID: 3156225
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular modeling predicts structural changes in the A subunit of factor XIII caused by two novel mutations identified in a neonate with severe congenital factor XIII deficiency.
    Souri M; Yee VC; Fujii N; Ichinose A
    Thromb Res; 2012 Sep; 130(3):506-10. PubMed ID: 22633530
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.