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 *

149 related articles for article (PubMed ID: 12567191)

  • 21. Haemophilia A mutations in patients with non-severe phenotype associated with a discrepancy between one-stage and chromogenic factor VIII activity assays.
    Pavlova A; Delev D; Pezeshkpoor B; Müller J; Oldenburg J
    Thromb Haemost; 2014 May; 111(5):851-61. PubMed ID: 24452774
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. F8 genetic analysis strategies when standard approaches fail.
    Pezeshkpoor B; Pavlova A; Oldenburg J; El-Maarri O
    Hamostaseologie; 2014; 34(2):167-73. PubMed ID: 24296544
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Creation of a novel donor splice site in intron 1 of the factor VIII gene leads to activation of a 191 bp cryptic exon in two haemophilia A patients.
    Bagnall RD; Waseem NH; Green PM; Colvin B; Lee C; Giannelli F
    Br J Haematol; 1999 Dec; 107(4):766-71. PubMed ID: 10606882
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N.
    Berber E; Fidanci ID; Un C; El-Maarri O; Aktuglu G; Gurgey A; Celkan T; Meral A; Oldenburg J; Graw J; Akar N; Caglayan H
    Haemophilia; 2006 Jul; 12(4):398-400. PubMed ID: 16834740
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. 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]  

  • 29. Factor VIII (FVIII) gene mutations in 120 patients with hemophilia A: detection of 26 novel mutations and correlation with FVIII inhibitor development.
    Repessé Y; Slaoui M; Ferrandiz D; Gautier P; Costa C; Costa JM; Lavergne JM; Borel-Derlon A
    J Thromb Haemost; 2007 Jul; 5(7):1469-76. PubMed ID: 17445092
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Application studies on the gene diagnosis and carrier detection of hemophilia A by using polymerase chain reaction-conformation sensitive gel electrophoresis].
    Lillicrap D; He GP; Leggo J; Liu YS; Tong XH; Zhou GX; Luo LH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):393-9. PubMed ID: 20017302
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Screening for mutations in haemophilia A patients by multiplex PCR-SSCP, Southern blotting and RNA analysis: the detection of a genetic abnormality in the factor VIII gene in 30 out of 35 patients.
    Pieneman WC; Deutz-Terlouw PP; Reitsma PH; Briët E
    Br J Haematol; 1995 Jun; 90(2):442-9. PubMed ID: 7794769
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mutations and a polymorphism in the factor VIII gene discovered by denaturing gradient gel electrophoresis.
    Kogan S; Gitschier J
    Proc Natl Acad Sci U S A; 1990 Mar; 87(6):2092-6. PubMed ID: 2107542
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular analysis of FVIII gene in severe HA patients of Costa Rica.
    Salazar-Sánchez L; Jiménez-Cruz G; Mendez M; Chaverri P; Alvarado P; Schröder W; Wulff K; Sandoval M; Herrmann FH; Pavlova A; Oldenburg J
    Hamostaseologie; 2010 Nov; 30 Suppl 1():S150-2. PubMed ID: 21052611
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Determinants of factor VIII plasma levels in carriers of haemophilia A and in control women.
    Ay C; Thom K; Abu-Hamdeh F; Horvath B; Quehenberger P; Male C; Mannhalter C; Pabinger I
    Haemophilia; 2010 Jan; 16(1):111-7. PubMed ID: 19758307
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Profiling of factor VIII mutations in Korean haemophilia A.
    Hwang SH; Kim MJ; Lim JA; Kim HC; Kim HS
    Haemophilia; 2009 Nov; 15(6):1311-7. PubMed ID: 19719548
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A.
    Lakich D; Kazazian HH; Antonarakis SE; Gitschier J
    Nat Genet; 1993 Nov; 5(3):236-41. PubMed ID: 8275087
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Analysis of the essential sequences of the factor VIII gene in twelve haemophilia A patients by single-stranded conformation polymorphism.
    David D; Moreira I; Lalloz MR; Rosa HA; Schwaab R; Morais S; Diniz MJ; de Deus G; Campos M; Lavinha J
    Blood Coagul Fibrinolysis; 1994 Apr; 5(2):257-64. PubMed ID: 8054459
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. A deletion/insertion leading to the generation of a direct repeat as a result of slipped mispairing and intragenic recombination in the factor VIII gene.
    Tavassoli K; Eigel A; Horst J
    Hum Genet; 1999 May; 104(5):435-7. PubMed ID: 10394938
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.