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 *

235 related articles for article (PubMed ID: 20331761)

  • 1. Spectrum of F8 gene mutations in haemophilia A patients from a region of Italy: identification of 23 new mutations.
    Riccardi F; Tagliaferri A; Martorana D; Rivolta GF; Valdrè L; Rodorigo G; Biasoli C; D'Incà M; Serino ML; Macchi S; Vincenzi D; Arbasi M; Pedrazzi P; Volta M; DI Perna C; Ippolito L; Savi M; Neri TM
    Haemophilia; 2010 Sep; 16(5):791-800. PubMed ID: 20331761
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Computational and molecular approaches for predicting unreported causal missense mutations in Belgian patients with haemophilia A.
    Lannoy N; Abinet I; Bosmans A; Lambert C; Vermylen C; Hermans C
    Haemophilia; 2012 May; 18(3):e331-9. PubMed ID: 21883705
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Canadian "National Program for hemophilia mutation testing" database: a ten-year review.
    Rydz N; Leggo J; Tinlin S; James P; Lillicrap D
    Am J Hematol; 2013 Dec; 88(12):1030-4. PubMed ID: 23913812
    [TBL] [Abstract][Full Text] [Related]  

  • 8. F8 mRNA studies in haemophilia A patients with different splice site mutations.
    Castaman G; Giacomelli SH; Mancuso ME; Sanna S; Santagostino E; Rodeghiero F
    Haemophilia; 2010 Sep; 16(5):786-90. PubMed ID: 20398075
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of 123 previously unreported mutations in the F8 gene of Iranian patients with haemophilia A.
    Ravanbod S; Rassoulzadegan M; Rastegar-Lari G; Jazebi M; Enayat S; Ala F
    Haemophilia; 2012 May; 18(3):e340-6. PubMed ID: 22117735
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. First report of molecular diagnosis of Tunisian hemophiliacs A: identification of 8 novel causative mutations.
    Elmahmoudi H; Khodjet-el-khil H; Wigren E; Jlizi A; Zahra K; Pellechia D; Vinciguerra C; Meddeb B; Elggaaied AB; Gouider E
    Diagn Pathol; 2012 Aug; 7():93. PubMed ID: 22883072
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A.
    Santacroce R; Acquila M; Belvini D; Castaldo G; Garagiola I; Giacomelli SH; Lombardi AM; Minuti B; Riccardi F; Salviato R; Tagliabue L; Grandone E; Margaglione M;
    J Hum Genet; 2008; 53(3):275-284. PubMed ID: 18217193
    [TBL] [Abstract][Full Text] [Related]  

  • 13. F8 gene dosage defects in atypical patients with severe haemophilia A.
    Venceslá Á; Baena M; Garrido RP; Núñez R; Velasco F; Rosell J; Villar A; Jiménez-Yuste V; Baiget M; Tizzano EF
    Haemophilia; 2012 Sep; 18(5):708-13. PubMed ID: 22621702
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Detection of 95 novel mutations in coagulation factor VIII gene F8 responsible for hemophilia A: results from a single institution.
    Guillet B; Lambert T; d'Oiron R; Proulle V; Plantier JL; Rafowicz A; Peynet J; Costa JM; Bendelac L; Laurian Y; Lavergne JM
    Hum Mutat; 2006 Jul; 27(7):676-85. PubMed ID: 16786531
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The molecular aetiology of haemophilia A in a New Zealand patient group.
    Laurie AD; Sheen CR; Hanrahan V; Smith MP; George PM
    Haemophilia; 2007 Jul; 13(4):420-7. PubMed ID: 17610560
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The identification and classification of 41 novel mutations in the factor VIII gene (F8C).
    Cutler JA; Mitchell MJ; Smith MP; Savidge GF
    Hum Mutat; 2002 Mar; 19(3):274-8. PubMed ID: 11857744
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of mutations in the F8 and F9 gene in families with haemophilia using targeted high-throughput sequencing.
    Lyu C; Xue F; Liu X; Liu W; Fu R; Sun T; Wu R; Zhang L; Li H; Zhang D; Yang R; Zhang L
    Haemophilia; 2016 Sep; 22(5):e427-34. PubMed ID: 27292088
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.