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 *

101 related articles for article (PubMed ID: 23492911)

  • 1. Unusual presentation of haemophilia in two paediatric patients.
    De Luca M; Carducci FI; Pansini V; Coletti V; Tucci FM; Cirillo M; Acquila M; Bicocchi MP; D'Argenio P; Luciani M
    Blood Coagul Fibrinolysis; 2013 Sep; 24(6):645-8. PubMed ID: 23492911
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Female haemophiliac homozygous for the factor VIII intron 22 inversion mutation, with transcriptional inactivation of one of the factor VIII alleles.
    David D; Morais S; Ventura C; Campos M
    Haemophilia; 2003 Jan; 9(1):125-30. PubMed ID: 12558791
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Severe haemophilia A in a preterm girl with Turner syndrome: case report - a diagnostic and therapeutic challenge for a paediatrician (Part 2).
    Agnieszka B; Monika WM; Barbara W; Anna K
    Ital J Pediatr; 2021 Jul; 47(1):157. PubMed ID: 34256805
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Prenatal diagnosis of haemophilia.
    Saxena R; Mohanty S; Choudhry VP
    Indian J Pediatr; 1998; 65(5):645-9. PubMed ID: 10773919
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Normalization of factor VIII levels in a patient with mild haemophilia A during a 35-year period.
    Mainwaring CJ; Evans J; Chana J; Lewis H
    Haemophilia; 2006 Nov; 12(6):668-71. PubMed ID: 17083519
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Heritable skewed X-chromosome inactivation leads to haemophilia A expression in heterozygous females.
    Renault NK; Dyack S; Dobson MJ; Costa T; Lam WL; Greer WL
    Eur J Hum Genet; 2007 Jun; 15(6):628-37. PubMed ID: 17342157
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Absence of correlation between X chromosome inactivation pattern and plasma concentration of factor VIII and factor IX in carriers of haemophilia A and B.
    Orstavik KH; Scheibel E; Ingerslev J; Schwartz M
    Thromb Haemost; 2000 Mar; 83(3):433-7. PubMed ID: 10744150
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of F8 defects in haemophilia A in Pakistan: investigation of correlation between mutation type and the in vitro thrombin generation assay.
    Khanum F; Collins PW; Harris RL; Bowen DJ
    Haemophilia; 2014 Mar; 20(2):287-93. PubMed ID: 24118398
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Haemophilia A and intracranial bleedings in infants].
    Peltier J; Baroncini M; Thines L; Leteurtre S; Marey A; Vinchon M
    Neurochirurgie; 2012 Feb; 58(1):19-24. PubMed ID: 22385799
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Liver haemorrhage in haemophilia--a case report and review of the literature.
    Hamilton M; French W; Rhymes N; Collins P
    Haemophilia; 2006 Jul; 12(4):441-3. PubMed ID: 16834749
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [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]  

  • 16. Diagnosis and management challenges in patients with mild haemophilia A and discrepant FVIII measurements.
    Trossaert M; Lienhart A; Nougier C; Fretigny M; Sigaud M; Meunier S; Fouassier M; Ternisien C; Negrier C; Dargaud Y
    Haemophilia; 2014 Jul; 20(4):550-8. PubMed ID: 24517184
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. [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]  

  • 19. Identification of de novo deletion in the factor VIII gene by MLPA technique in two girls with isolated factor VIII deficiency.
    Lannoy N; Abinet I; Dahan K; Hermans C
    Haemophilia; 2009 May; 15(3):797-801. PubMed ID: 19432928
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Incidence and risk factors for inhibitor development in previously untreated severe haemophilia A patients born between 2005 and 2010.
    Vézina C; Carcao M; Infante-Rivard C; Lillicrap D; Stain AM; Paradis E; Teitel J; Rivard GE;
    Haemophilia; 2014 Nov; 20(6):771-6. PubMed ID: 25039669
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.