667 related articles for article (PubMed ID: 24503678)
1. 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]
2. 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]
3. 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]
4. Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations.
Katona É; Muszbek L; Devreese K; Kovács KB; Bereczky Z; Jonkers M; Shemirani AH; Mondelaers V; Ermens AA
Haemophilia; 2014 Jan; 20(1):114-20. PubMed ID: 24118344
[TBL] [Abstract][Full Text] [Related]
5. Biology of Factor XIII and clinical manifestations of Factor XIII deficiency.
Levy JH; Greenberg C
Transfusion; 2013 May; 53(5):1120-31. PubMed ID: 22928875
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Factor XIII deficiency.
Hsieh L; Nugent D
Haemophilia; 2008 Nov; 14(6):1190-200. PubMed ID: 19141159
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Identification of a novel mutation in the factor XIII A subunit in a patient with inherited factor XIII deficiency.
Yan L; Wang T; Qiu J; Zhang X; Peng J; Fang Y; Sheng Z
Int J Hematol; 2023 Jul; 118(1):26-35. PubMed ID: 37059930
[TBL] [Abstract][Full Text] [Related]
12. Neoplasm-induced bleeding in inherited, heterozygous FXIII-A deficiency.
Ivaškevičius V; Goldmann G; Biswas A; Westhofen P; Thomas A; Marquardt N; Horneff S; Klein C; Rühl H; Pötzsch B; Oldenburg J
Hamostaseologie; 2015; 35 Suppl 1():S32-5. PubMed ID: 26540128
[TBL] [Abstract][Full Text] [Related]
13. Heterozygosity in factor XIII genes and the manifestation of mild inherited factor XIII deficiency.
Singh S; Pezeshkpoor B; Jamil MA; Dodt J; Sharma A; Ramar V; Ivaskevicius V; Hethershaw E; Philippou H; Pavlova A; Oldenburg J; Biswas A
J Thromb Haemost; 2024 Feb; 22(2):379-393. PubMed ID: 37832789
[TBL] [Abstract][Full Text] [Related]
14. [Acquired autoimmune coagulation factor XIII/13 deficiency].
Ogawa Y
Rinsho Ketsueki; 2020; 61(7):799-808. PubMed ID: 32759568
[TBL] [Abstract][Full Text] [Related]
15. Comparison of F13A1 gene mutations in 73 patients treated with recombinant FXIII-A
Ivaškevičius V; Biswas A; Garly ML; Oldenburg J
Haemophilia; 2017 May; 23(3):e194-e203. PubMed ID: 28520207
[TBL] [Abstract][Full Text] [Related]
16. [Factor XIII deficiency - not only a congenital bleeding disorder].
Schött U; Astermark J; Zdanowski A; Strandberg K
Lakartidningen; 2023 Apr; 120():. PubMed ID: 37099358
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. 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
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]