BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

366 related articles for article (PubMed ID: 18371166)

  • 1. Spectrum of factor VIII mutations in Arab patients with severe haemophilia A.
    Abu-Amero KK; Hellani A; Al-Mahed M; Al-Sheikh I
    Haemophilia; 2008 May; 14(3):484-8. PubMed ID: 18371166
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions.
    Jayandharan G; Shaji RV; Baidya S; Nair SC; Chandy M; Srivastava A
    Haemophilia; 2005 Sep; 11(5):481-91. PubMed ID: 16128892
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Detection of factor VIII intron 1 inversion in severe haemophilia A].
    Liang Y; Yan ZY; Yan M; Hua BL; Xiao B; Zhao YQ; Liu JZ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):323-5. PubMed ID: 19504449
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic analysis of haemophilia A in Taiwan.
    Chen YC; Hu SH; Cheng SN; Chao TY
    Haemophilia; 2010 May; 16(3):538-44. PubMed ID: 20236351
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Molecular genetics of hemophilia A].
    De Brasi CD; Slavutsky IR; Larripa IB
    Medicina (B Aires); 1996; 56(5 Pt 1):509-17. PubMed ID: 9239887
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular genotyping of hemophilia A in Saudi Arabia: report of 2 novel mutations.
    Owaidah TM; Alkhail HA; Zahrani HA; Musa AA; Saleh MA; Riash MA; Alodaib A; Abu Amero K
    Blood Coagul Fibrinolysis; 2009 Sep; 20(6):415-8. PubMed ID: 19448530
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Spectrum of mutations in Albanian patients with haemophilia A: identification of ten novel mutations in the factor VIII gene.
    Castaman G; Giacomelli SH; Ghiotto R; Boseggia C; Pojani K; Bulo A; Madeo D; Rodeghiero F
    Haemophilia; 2007 May; 13(3):311-6. PubMed ID: 17498081
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Study of mutations in Jordanian patients with haemophilia A: identification of five novel mutations.
    Awidi A; Ramahi M; Alhattab D; Mefleh R; Dweiri M; Bsoul N; Magablah A; Arafat E; Barqawi M; Bishtawi M; Haddadeen E; Falah M; Tarawneh B; Swaidan S; Fauori S
    Haemophilia; 2010 Jan; 16(1):136-42. PubMed ID: 19817879
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation analysis in 51 patients with haemophilia A: report of 10 novel mutations and correlations between genotype and clinical phenotype.
    Hill M; Deam S; Gordon B; Dolan G
    Haemophilia; 2005 Mar; 11(2):133-41. PubMed ID: 15810915
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutational spectrum of F8 gene and prothrombotic gene variants in haemophilia A patients from Southern Italy.
    Sanna V; Zarrilli F; Nardiello P; D'Argenio V; Rocino A; Coppola A; DI Minno G; Castaldo G
    Haemophilia; 2008 Jul; 14(4):796-803. PubMed ID: 18459951
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Relationship between factor VIII mutation type and inhibitor development in a cohort of previously untreated patients treated with recombinant factor VIII (Recombinate). Recombinate PUP Study Group.
    Goodeve AC; Williams I; Bray GL; Peake IR
    Thromb Haemost; 2000 Jun; 83(6):844-8. PubMed ID: 10896236
    [TBL] [Abstract][Full Text] [Related]  

  • 12. High throughput mutation screening of the factor VIII gene (F8C) in hemophilia A: 37 novel mutations and genotype-phenotype correlation.
    Citron M; Godmilow L; Ganguly T; Ganguly A
    Hum Mutat; 2002 Oct; 20(4):267-74. PubMed ID: 12325022
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular analysis of F8 in Lebanese haemophilia A patients: novel mutations and phenotype-genotype correlation.
    Djambas Khayat C; Salem N; Chouery E; Corbani S; Moix I; Nicolas E; Morris MA; de Moerloose P; Mégarbané A
    Haemophilia; 2008 Jul; 14(4):709-16. PubMed ID: 18479430
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Intron 1 and 22 inversions in factor VIII gene in patients with haemophilia A].
    Li T; Dai J; Wu JS; Ding QL; Ding KY; Zheng CC; Sun P; Wang XF
    Zhonghua Xue Ye Xue Za Zhi; 2009 Mar; 30(3):150-3. PubMed ID: 19642360
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A.
    Bogdanova N; Markoff A; Pollmann H; Nowak-Göttl U; Eisert R; Dworniczak B; Eigel A; Horst J
    Hum Mutat; 2002 Sep; 20(3):236-7. PubMed ID: 12204009
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of factor VIII gene mutations in patients with severe haemophilia A in Venezuela: identification of seven novel mutations.
    Albánez S; Ruiz-Sáez A; Boadas A; de Bosch N; Porco A
    Haemophilia; 2011 Sep; 17(5):e913-8. PubMed ID: 21371196
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterisation of 96 mutations in 128 unrelated severe haemophilia A patients from France. Description of 62 novel mutations.
    Vinciguerra C; Zawadzki C; Dargaud Y; Pernod G; Berger C; Nougier C; Négrier C
    Thromb Haemost; 2006 Apr; 95(4):593-9. PubMed ID: 16601827
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analysis of large structural changes of the factor VIII gene, involving intron 1 and 22, in severe hemophilia A.
    Andrikovics H; Klein I; Bors A; Nemes L; Marosi A; Váradi A; Tordai A
    Haematologica; 2003 Jul; 88(7):778-84. PubMed ID: 12857556
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Long distance PCR in detection of inversion mutations of F8C gene in hemophilia A patients.
    Poláková H; Zmetáková I; Kádasi L
    Gen Physiol Biophys; 2003 Jun; 22(2):243-53. PubMed ID: 14699993
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Seven novel and four recurrent point mutations in the factor VIII (F8C) gene.
    Bogdanova N; Lemcke B; Markoff A; Pollmann H; Dworniczak B; Eigel A; Horst J
    Hum Mutat; 2001 Dec; 18(6):546. PubMed ID: 11748850
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.