These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

312 related articles for article (PubMed ID: 15921397)

  • 1. The spectrum of mutations in Southern Spanish patients with hemophilia A and identification of 28 novel mutations.
    Fernández-López O; García-Lozano JR; Núñez-Vázquez R; Pérez-Garrido R; Núñez-Roldán A
    Haematologica; 2005 May; 90(5):707-10. PubMed ID: 15921397
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rapid hemophilia A molecular diagnosis by a simple DNA sequencing procedure: identification of 14 novel mutations.
    Vidal F; Farssac E; Altisent C; Puig L; Gallardo D
    Thromb Haemost; 2001 Apr; 85(4):580-3. PubMed ID: 11341489
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of 32 novel mutations in the factor VIII gene in Indian patients with hemophilia A.
    Ahmed RP; Ivaskevicius V; Kannan M; Seifried E; Oldenburg J; Saxena R
    Haematologica; 2005 Feb; 90(2):283-4. PubMed ID: 15710596
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Spectrum of molecular defects and mutation detection rate in patients with severe hemophilia A.
    Bogdanova N; Markoff A; Pollmann H; Nowak-Göttl U; Eisert R; Wermes C; Todorova A; Eigel A; Dworniczak B; Horst J
    Hum Mutat; 2005 Sep; 26(3):249-54. PubMed ID: 16086318
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Non-inversion factor VIII mutations in 80 hemophilia A families including 24 with alloimmune responses.
    Liu ML; Nakaya S; Thompson AR
    Thromb Haemost; 2002 Feb; 87(2):273-6. PubMed ID: 11858487
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Molecular characterization of hemophilia B in North Indian families: identification of novel and recurrent molecular events in the factor IX gene.
    Mahajan A; Chavali S; Kabra M; Chowdhury MR; Bharadwaj D
    Haematologica; 2004 Dec; 89(12):1498-503. PubMed ID: 15590401
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular diagnostics of 15 hemophilia A patients: characterization of eight novel mutations in the factor VIII gene, two of which result in exon skipping.
    Tavassoli K; Eigel A; Wilke K; Pollmann H; Horst J
    Hum Mutat; 1998; 12(5):301-3. PubMed ID: 9792405
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutational-screening in the factor VIII gene resulting in the identification of three novel mutations, one of which is a donor splice mutation. Mutations in brief no. 245. Online.
    Möller-Morlang K; Tavassoli K; Eigel A; Pollmann H; Horst J
    Hum Mutat; 1999; 13(6):504. PubMed ID: 10408784
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype.
    Margaglione M; Castaman G; Morfini M; Rocino A; Santagostino E; Tagariello G; Tagliaferri AR; Zanon E; Bicocchi MP; Castaldo G; Peyvandi F; Santacroce R; Torricelli F; Grandone E; Mannucci PM;
    Haematologica; 2008 May; 93(5):722-8. PubMed ID: 18387975
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Inversion mutation as a major cause of severe hemophilia A in Italian patients.
    Mori PG; Caprino D; Bicocchi MP; Valetto A; Bottini F; Aquila M
    Haematologica; 1997; 82(1):75-6. PubMed ID: 9107090
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.