BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 30578706)

  • 1. Factor XIII mutation spectrum in Iranian patients with hereditary factor XIII deficiency: Detection of 3 novel mutations.
    Mirakhorli M; Behboudi Farahbakhsh F; Reza Baghaipour M; Mahmoudi T; Jazebi M; Tabatabaei SM; Aala F
    Int J Lab Hematol; 2019 Jun; 41(3):e61-e65. PubMed ID: 30578706
    [No Abstract]   [Full Text] [Related]  

  • 2. Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran.
    Eshghi P; Cohan N; Lak M; Naderi M; Peyvandi F; Menegatti M; Karimi M
    Clin Appl Thromb Hemost; 2012; 18(1):100-3. PubMed ID: 22156982
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Molecular genetic analysis of ten unrelated Iranian patients with congenital factor XIII deficiency.
    Dorgalaleh A; Tabibian S; Bamedi T; Tamaddon GH; Naderi M; Varmaghani B; Boustani H; Dadashizadeh G
    Int J Lab Hematol; 2017 Apr; 39(2):e33-e36. PubMed ID: 28013530
    [No Abstract]   [Full Text] [Related]  

  • 6. Identification of two novel missense mutations causing severe factor XIII deficiency.
    Handrkova H; Borhany M; Schroeder V; Fatima N; Hussain A; Shamsi T; Kohler HP
    Haemophilia; 2015 May; 21(3):e253-e256. PubMed ID: 25832324
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. Mutations in coagulation factor XIII A gene in three Turkish patients: two novel mutations and a known insertion.
    Birben E; Oner R; Oner C; Gümrük F; Altay C; Gürgey A
    Br J Haematol; 2002 Jul; 118(1):278-81. PubMed ID: 12100162
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Seven novel mutations in the factor XIII A-subunit gene causing hereditary factor XIII deficiency in 10 unrelated families.
    Vysokovsky A; Saxena R; Landau M; Zivelin A; Eskaraev R; Rosenberg N; Seligsohn U; Inbal A
    J Thromb Haemost; 2004 Oct; 2(10):1790-7. PubMed ID: 15456491
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of novel pathogenic F13A1 mutation and novel NBEAL2 gene missense mutation in a pedigree with hereditary congenital factor XIII deficiency.
    Jia S; He Y; Lu M; Liao N; Lei Y; Lauriane N; Liang K; Wei H
    Gene; 2019 Jun; 702():143-147. PubMed ID: 30935919
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel compound heterozygous mutation in the F13A gene causing hereditary factor XIII deficiency in a Chinese family.
    Wu S; Wang Z; Dong N; Bai X; Ruan C
    J Thromb Haemost; 2006 Jan; 4(1):267-9. PubMed ID: 16409483
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Molecular mechanisms of two novel mutations of factor XIII gene resulting in hereditary coagulation deficiency].
    Duan BH; Wang HL; Wang XF; Hu YQ; Chu HY; Wang H; Yin J; Guo XM; Fu QH; Wu WM; Ding QL; Fang Y; Wang WB; Zhou RF; Kang WY; Xie S; Wang ZY
    Zhonghua Yi Xue Za Zhi; 2003 Dec; 83(24):2158-61. PubMed ID: 14720426
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Further evidence of heterogeneity of gene defects in Italian families with factor XIII deficiency.
    Castaman G; Giacomelli SH; Schroeder V; Sanna S; Valdrè L; Morfini M; Banov L; Kohler HP; Rodeghiero F
    Haemophilia; 2012 Jan; 18(1):e6-8. PubMed ID: 21812861
    [No Abstract]   [Full Text] [Related]  

  • 19. Spontaneous splenic rupture in a patient with factor XIII deficiency and a novel mutation.
    Khalife H; Muwakkit S; Al-Moussawi H; Dabbous I; Khoury R; Peyvandi F; Abboud MR
    Pediatr Blood Cancer; 2008 Jan; 50(1):113-4. PubMed ID: 16456856
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.