150 related articles for article (PubMed ID: 32776739)
1. Premarital Screening Program for Congenital Factor XIII Deficiency in Iran.
Daneshi M; Dorgalaleh A; Tabibian S; Safa M; Naderi M; Kazemi A
Clin Lab; 2020 Aug; 66(8):. PubMed ID: 32776739
[TBL] [Abstract][Full Text] [Related]
2. First cases of severe congenital factor XIII deficiency in Southwestern Afghanistan in the vicinity of southeast of Iran.
Hosseini S; Dorgalaleh A; Bamedi T; Tavakol K; Tabibian S; Naderi M; Alizadeh S; Varmaghani B; Shamsizadeh M; Rahimizadeh A; Ebrahimi S
Blood Coagul Fibrinolysis; 2015 Dec; 26(8):908-11. PubMed ID: 26226252
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Noninvasive prenatal diagnosis of congenital factor XIII deficiency in Iran.
Motlagh H; Dorgalaleh A; Tabibian S; Naderi M; Zaker F
Blood Coagul Fibrinolysis; 2022 Apr; 33(3):167-170. PubMed ID: 34980832
[TBL] [Abstract][Full Text] [Related]
5. Establishment of a prenatal diagnosis schedule as part of a prophylaxis program of factor XIII deficiency in the southeast of Iran.
Naderi M; Reykande SE; Dorgalaleh A; Alizadeh S; Tabibian S; Einollahi N; Moghaddam EM
Blood Coagul Fibrinolysis; 2016 Jan; 27(1):97-100. PubMed ID: 26703985
[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. Molecular Basis of Congenital Factor XIII Deficiency in Iran.
Dorgalaleh A; Assadollahi V; Tabibian S; Shamsizadeh M
Clin Appl Thromb Hemost; 2018 Mar; 24(2):210-216. PubMed ID: 27879471
[TBL] [Abstract][Full Text] [Related]
8. 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; 89(5):499-504. PubMed ID: 19937244
[TBL] [Abstract][Full Text] [Related]
9. The most common disease-causing mutation of factor XIII deficiency is corrected by CRISPR/CAS9 gene editing system.
Dorgalaleh A; Kiani J; Zaker F; Safa M
Blood Coagul Fibrinolysis; 2022 Apr; 33(3):153-158. PubMed ID: 35221320
[TBL] [Abstract][Full Text] [Related]
10. Challenges in implementation of ISTH diagnostic algorithm for diagnosis and classification of factor XIII deficiency in Iran.
Dorgalaleh A; Farshi Y; Alizadeh SH; Naderi M; Tabibian SH; Kazemi A; Hosseini S
J Thromb Haemost; 2015 Sep; 13(9):1735-6. PubMed ID: 26099358
[No Abstract] [Full Text] [Related]
11. 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]
12. Factor XIII Deficiency in Western Afghanistan due to a Novel F13A Gene Mutation.
Mousavi SH; Zeinali S; Mesbah-Namin SA; Shams M; Dorgalaleh A
Int J Lab Hematol; 2020 Feb; 42(1):e1-e3. PubMed ID: 31136071
[No Abstract] [Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. Application of HUMF13A01 (AAAG)n STR polymorphism to the genetic diagnosis of coagulation factor XIII deficiency.
Kangsadalampai S; Coggan M; Caglayan SH; Aktuglu G; Board PG
Thromb Haemost; 1996 Dec; 76(6):879-82. PubMed ID: 8972004
[TBL] [Abstract][Full Text] [Related]
17. A novel Cys328-terminator mutant implicated in severe coagulation factor XIII deficiency: a case report.
Cai R; Li Y; Wang W; Feng Q
BMC Med Genet; 2020 Sep; 21(1):175. PubMed ID: 32883222
[TBL] [Abstract][Full Text] [Related]
18. Morbidity and mortality in a large number of Iranian patients with severe congenital factor XIII deficiency.
Dorgalaleh A; Naderi M; Shamsizadeh M
Ann Hematol; 2016 Feb; 95(3):451-5. PubMed ID: 26692088
[TBL] [Abstract][Full Text] [Related]
19. Molecular diagnosis of factor XIII deficiency, data from comprehensive coagulation laboratory in Iran.
Gheidishahran M; Dorgalaleh A; Tabibian S; Shams M; Sanei Moghaddam E; Khosravi S; Naderi M; Kahraze S; Lotfi F; Kazeme A; Safa M
Blood Coagul Fibrinolysis; 2018 Jan; 29(1):87-91. PubMed ID: 29095761
[TBL] [Abstract][Full Text] [Related]
20. Pathogenicity analysis of variations and prenatal diagnosis in a hereditary coagulation factor XIII deficiency family.
Sun L; Yan Q; Wang Y; Luo H; Du P; Hassan R; Liu L; Jiang W
Hematology; 2018 Sep; 23(8):501-509. PubMed ID: 29307277
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
