146 related articles for article (PubMed ID: 36940714)
1. Novel Insights into Heterozygous Factor XIII Deficiency.
Dorgalaleh A
Semin Thromb Hemost; 2024 Mar; 50(2):200-212. PubMed ID: 36940714
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Central nervous system bleeding in pediatric patients with factor XIII deficiency: a study on 23 new cases.
Naderi M; Alizadeh S; Kazemi A; Tabibian S; Zaker F; Bamedi T; Kashani Khatib Z; Dorgalaleh A
Hematology; 2015 Mar; 20(2):112-8. PubMed ID: 25001244
[TBL] [Abstract][Full Text] [Related]
4. A Unique Factor XIII Mutation in Southeastern Iran with an Unexpectedly High Prevalence: Khash Factor XIII.
Dorgalaleh A; Tabibian S; Shams M; Majid G; Naderi M; Casini A; Tavasoli B; Gheidishiran M; Daneshi M; Safa M
Semin Thromb Hemost; 2019 Feb; 45(1):43-49. PubMed ID: 30630205
[TBL] [Abstract][Full Text] [Related]
5. Clinical manifestations and management of life-threatening bleeding in the largest group of patients with severe factor XIII deficiency.
Naderi M; Dorgalaleh A; Alizadeh S; Tabibian S; Hosseini S; Shamsizadeh M; Bamedi T
Int J Hematol; 2014 Nov; 100(5):443-9. PubMed ID: 25230816
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Blood coagulation factor XIII and factor XIII deficiency.
Dorgalaleh A; Rashidpanah J
Blood Rev; 2016 Nov; 30(6):461-475. PubMed ID: 27344554
[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. 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]
10. 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]
11. 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]
12. 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]
13. [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]
14. Postpartum Hemorrhage in Heterozygote Factor XIII Deficient Women Compared With Healthy Women. A Cross-Sectional Experience From Iran.
Naderi M; Mirzaei I; Yaghoubi S; Milani I; Cohan N
Clin Appl Thromb Hemost; 2021; 27():10760296211051714. PubMed ID: 34697946
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. The impact of acquired coagulation factor XIII deficiency in traumatic bleeding and wound healing.
Kleber C; Sablotzki A; Casu S; Olivieri M; Thoms KM; Horter J; Schmitt FCF; Birschmann I; Fries D; Maegele M; Schöchl H; Wilhelmi M
Crit Care; 2022 Mar; 26(1):69. PubMed ID: 35331308
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Two novel and one recurrent missense mutation in the factor XIII A gene in two Dutch patients with factor XIII deficiency.
Gómez García EB; Poort SR; Stibbe J; Sturk A; Schaap MC; Kappers M; Bertina RM
Br J Haematol; 2001 Feb; 112(2):513-8. PubMed ID: 11167856
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
