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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

377 related items for PubMed ID: 16456856

  • 1. Spontaneous splenic rupture in a patient with factor XIII deficiency and a novel mutation.
    Khalife H, Muwakkit S, Al-Moussawi H, Dabbous I, Khoury R, Peyvandi F, Abboud MR.
    Pediatr Blood Cancer; 2008 Jan; 50(1):113-4. PubMed ID: 16456856
    [Abstract] [Full Text] [Related]

  • 2. [Spontaneous splenic rupture in a patient with congenital factor XIII deficiency].
    Toubouras M, Panagopoulos F, Makris G.
    Chirurg; 1980 Jan; 51(1):46-7. PubMed ID: 7389494
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Gene defects in congenital factor XIII deficiency.
    Mikkola H, Palotie A.
    Semin Thromb Hemost; 1996 Jan; 22(5):393-8. PubMed ID: 8989822
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. [Characterization of a large deletion that leads to congenital factor XIII deficiency].
    Otaki M, Inaba H, Shinozawa K, Fujita S, Amano K, Fukutake K.
    Rinsho Byori; 2008 Mar; 56(3):187-94. PubMed ID: 18411802
    [Abstract] [Full Text] [Related]

  • 9. Spontaneous epidural hematoma in a child with inherited factor XIII deficiency.
    Farah RA, Al Danaf JZ, Chahinian RA, Braiteh NT, Al Ojaimi NF, Cairo A, Farhat H, Mantoura JR.
    J Pediatr Hematol Oncol; 2014 Jan; 36(1):62-5. PubMed ID: 23619114
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Deficiency of coagulation factor XIII A subunit caused by the dinucleotide deletion at the 5' end of exon III.
    Kamura T, Okamura T, Murakawa M, Tsuda H, Teshima T, Shibuya T, Harada M, Niho Y.
    J Clin Invest; 1992 Aug; 90(2):315-9. PubMed ID: 1644910
    [Abstract] [Full Text] [Related]

  • 12. Molecular characterization of a novel mutation in the factor XIII a subunit gene associated with a severe defect: importance of prophylactic substitution.
    Morange P, Trigui N, Frère C, Chambost H, Pouymayou C, Uters M, Boucly C, Juhan-Vague I, de Mazancourt P.
    Blood Coagul Fibrinolysis; 2009 Oct; 20(7):605-6. PubMed ID: 19713833
    [Abstract] [Full Text] [Related]

  • 13. Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutations.
    Ivaskevicius V, Windyga J, Baran B, Schroeder V, Junen J, Bykowska K, Seifried E, Kohler HP, Oldenburg J.
    Haemophilia; 2007 Sep; 13(5):649-57. PubMed ID: 17880458
    [Abstract] [Full Text] [Related]

  • 14. [Molecular mechanisms of two novel mutations of factor XIII gene resulting in hereditary coagulation deficiency].
    Duan BH, Wang HL, Wang XF, Hu YQ, Chu HY, Wang H, Yin J, Guo XM, Fu QH, Wu WM, Ding QL, Fang Y, Wang WB, Zhou RF, Kang WY, Xie S, Wang ZY.
    Zhonghua Yi Xue Za Zhi; 2003 Dec 25; 83(24):2158-61. PubMed ID: 14720426
    [Abstract] [Full Text] [Related]

  • 15. [Identification of a novel mutation of F (13) A gene in a pedigree with factor XIII deficiency].
    Jiao WY, Wu JS, Ding QL, Wang XF, Xu XC, Ding KY, Liu X.
    Zhonghua Xue Ye Xue Za Zhi; 2007 Sep 25; 28(9):598-601. PubMed ID: 18246815
    [Abstract] [Full Text] [Related]

  • 16. An unusual clinical presentation of factor XIII deficiency and issues relating to the monitoring of factor XIII replacement therapy.
    Dargaud Y, de Mazancourt P, Rugeri L, Hanss M, Borg JY, Gaucherand P, Negrier C, Trzeciak C.
    Blood Coagul Fibrinolysis; 2008 Jul 25; 19(5):447-52. PubMed ID: 18600098
    [Abstract] [Full Text] [Related]

  • 17. Congenital factor XIII deficiency caused by two mutations in eight Tunisian families: molecular confirmation of a founder effect.
    Louhichi N, Medhaffar M, Hadjsalem I, Mkaouar-Rebai E, Fendri-Kriaa N, Kanoun H, Yaïch F, Souissi T, Elloumi M, Fakhfakh F.
    Ann Hematol; 2010 May 25; 89(5):499-504. PubMed ID: 19937244
    [Abstract] [Full Text] [Related]

  • 18. [Factor XIII deficiency due to lack of both the S and A subunits. (Classification of factor XIII deficiency in 2 groups)].
    Girolami A, Burul A, Cappellato MG, Betterle C, Casonato A, Dal Bo Zanon R.
    Ric Clin Lab; 1979 May 25; 9(2 Suppl):35-49. PubMed ID: 395620
    [No Abstract] [Full Text] [Related]

  • 19. 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 25; 20(2):255-62. PubMed ID: 24286209
    [Abstract] [Full Text] [Related]

  • 20. International registry on factor XIII deficiency: a basis formed mostly on European data.
    Ivaskevicius V, Seitz R, Kohler HP, Schroeder V, Muszbek L, Ariens RA, Seifried E, Oldenburg J, Study Group.
    Thromb Haemost; 2007 Jun 25; 97(6):914-21. PubMed ID: 17549292
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 19.