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272 related items for PubMed ID: 23619114
1. 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]
2. Efficacy and safety of prophylactic treatment with plasma-derived factor XIII concentrate (human) in patients with congenital factor XIII deficiency. Ashley C, Chang E, Davis J, Mangione A, Frame V, Nugent DJ. Haemophilia; 2015 Jan; 21(1):102-8. PubMed ID: 25377187 [Abstract] [Full Text] [Related]
5. 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]
7. Pharmacokinetics of recombinant factor XIII in young children with congenital FXIII deficiency and comparison with older patients. Williams M, Will A, Stenmo C, Rosholm A, Tehranchi R. Haemophilia; 2014 Jan; 20(1):99-105. PubMed ID: 23834599 [Abstract] [Full Text] [Related]
10. Recombinant factor XIII prophylaxis is safe and effective in young children with congenital factor XIII-A deficiency: international phase 3b trial results. Kerlin BA, Inbal A, Will A, Williams M, Garly ML, Jacobsen L, Kearney SL. J Thromb Haemost; 2017 Aug; 15(8):1601-1606. PubMed ID: 28581691 [Abstract] [Full Text] [Related]
12. 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 [Abstract] [Full Text] [Related]
13. Use of Factor XIII (FXIII) concentrate in patients with congenital FXIII deficiency undergoing surgical procedures. Janbain M, Nugent DJ, Powell JS, St-Louis J, Frame VB, Leissinger CA. Transfusion; 2015 Jan; 55(1):45-50. PubMed ID: 25070582 [Abstract] [Full Text] [Related]
16. Alloantibodies against the B subunit of plasma factor XIII developed in its congenital deficiency. Wada H, Souri M, Matsumoto R, Sugihara T, Ichinose A. Thromb Haemost; 2013 Apr; 109(4):661-8. PubMed ID: 23407795 [Abstract] [Full Text] [Related]
17. 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]