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.
159 related articles for article (PubMed ID: 24889649)
21. Factor XIII deficiency: an update. Schroeder V; Kohler HP Semin Thromb Hemost; 2013 Sep; 39(6):632-41. PubMed ID: 23929307 [TBL] [Abstract][Full Text] [Related]
22. Molecular mechanisms of mutations in factor XIII A-subunit deficiency: in vitro expression in COS-cells demonstrates intracellular degradation of the mutant proteins. Mikkola H; Muszbek L; Haramura G; Hämäläinen E; Jalanko A; Palotie A Thromb Haemost; 1997 Jun; 77(6):1068-72. PubMed ID: 9241733 [TBL] [Abstract][Full Text] [Related]
23. Factor XIII Deficiency. Karimi M; Bereczky Z; Cohan N; Muszbek L Semin Thromb Hemost; 2009 Jun; 35(4):426-38. PubMed ID: 19598071 [TBL] [Abstract][Full Text] [Related]
24. [Identification of genetic defects in a Chinese pedigree with factor XIII deficiency: case report and literature review]. Xu G; Liang Q; Zhang L; Shen Y; Ding Q; Wang X; Wang H Zhonghua Xue Ye Xue Za Zhi; 2015 Oct; 36(10):844-8. PubMed ID: 26477763 [TBL] [Abstract][Full Text] [Related]
25. A common F13A1 intron 1 variant IVS1+12(A) is associated with mild FXIII deficiency in Caucasian population. Ivaskevicius V; Biswas A; Thomas A; Lyonga S; Rott H; Halimeh S; Kappert G; Klammroth R; Scholz U; Eberl W; Harbrecht U; Gnida C; Hertfelder HJ; Marquardt N; Oldenburg J Ann Hematol; 2013 Jul; 92(7):975-9. PubMed ID: 23508224 [TBL] [Abstract][Full Text] [Related]
26. Phenotype and genotype of FXIII deficiency in two unrelated probands: identification of a novel F13A1 large deletion mediated by complex rearrangement. Ma S; Chen C; Liang Q; Wu X; Wang X; Wu W; Liu Y; Ding Q Orphanet J Rare Dis; 2019 Jul; 14(1):182. PubMed ID: 31340840 [TBL] [Abstract][Full Text] [Related]
27. Gene defects in congenital factor XIII deficiency. Mikkola H; Palotie A Semin Thromb Hemost; 1996; 22(5):393-8. PubMed ID: 8989822 [TBL] [Abstract][Full Text] [Related]
28. Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function. Ivaskevicius V; Biswas A; Bevans C; Schroeder V; Kohler HP; Rott H; Halimeh S; Petrides PE; Lenk H; Krause M; Miterski B; Harbrecht U; Oldenburg J Haematologica; 2010 Jun; 95(6):956-62. PubMed ID: 20179087 [TBL] [Abstract][Full Text] [Related]
29. Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired forms. Biswas A; Ivaskevicius V; Thomas A; Oldenburg J Hamostaseologie; 2014; 34(2):160-6. PubMed ID: 24503678 [TBL] [Abstract][Full Text] [Related]
30. Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parent. Shen MC; Chen M; Chang SP; Lin PT; Hsieh HN; Lin KH Pediatr Hematol Oncol; 2018; 35(7-8):442-446. PubMed ID: 30702381 [TBL] [Abstract][Full Text] [Related]
31. Molecular mechanism of a mild phenotype in coagulation factor XIII (FXIII) deficiency: a splicing mutation permitting partial correct splicing of FXIII A-subunit mRNA. Mikkola H; Muszbek L; Laiho E; Syrjälä M; Hämäläinen E; Haramura G; Salmi T; Peltonen L; Palotie A Blood; 1997 Feb; 89(4):1279-87. PubMed ID: 9028951 [TBL] [Abstract][Full Text] [Related]
32. [Identification of two novel mutation in two Chinese hereditary coagulation factor XIII deficiency families]. Duan B; Wang H; Chu H; Wang X; Qu B; Li D; Wang H; Yin J; Kang W; Wang Z Zhonghua Xue Ye Xue Za Zhi; 2002 Mar; 23(3):117-20. PubMed ID: 12015062 [TBL] [Abstract][Full Text] [Related]
34. Mild factor XIII deficiency and concurrent hypofibrinogenemia: effect of pregnancy. Kaveney AD; Philipp CS Blood Coagul Fibrinolysis; 2016 Jun; 27(4):457-60. PubMed ID: 26575494 [TBL] [Abstract][Full Text] [Related]
35. Effect of four missense mutations in the factor XIII A-subunit gene on protein stability: studies with recombinant proteins. Vysokovsky A; Rosenberg N; Dardik R; Seligsohn U; Inbal A Blood Coagul Fibrinolysis; 2006 Mar; 17(2):125-30. PubMed ID: 16479194 [TBL] [Abstract][Full Text] [Related]
36. Factor XIII deficiency: new nonsense and deletion mutations in the human factor XIIIA gene. Anwar R; Gallivan L; Richards M; Khair K; Wright M; Minford A Haematologica; 2005 Dec; 90(12):1718-20. PubMed ID: 16330458 [TBL] [Abstract][Full Text] [Related]
37. Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiency. Ivaskevicius V; Biswas A; Loreth R; Schroeder V; Ohlenforst S; Rott H; Krause M; Kohler HP; Scharrer I; Oldenburg J Haemophilia; 2010 Jul; 16(4):675-82. PubMed ID: 20331752 [TBL] [Abstract][Full Text] [Related]
38. 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]
39. Identification of a new mutation (Gly420Ser), distal to the active site, that leads to factor XIII deficiency. Kangsadalampai S; Yenchitsomanus P; Chelvanayagam G; Sawasdee N; Laosombat V; Board P Eur J Haematol; 2000 Oct; 65(4):279-84. PubMed ID: 11073170 [TBL] [Abstract][Full Text] [Related]
40. 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; Thromb Haemost; 2007 Jun; 97(6):914-21. PubMed ID: 17549292 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]