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 *

202 related articles for article (PubMed ID: 1905206)

  • 1. Prevention and control of haemophilia: memorandum from a joint WHO/WFH meeting (World Federation of Haemophilia).
    Bull World Health Organ; 1991; 69(1):17-26. PubMed ID: 1905206
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Haemophilia: strategies for carrier detection and prenatal diagnosis.
    Peake IR; Lillicrap DP; Boulyjenkov V; Briet E; Chan V; Ginter EK; Kraus EM; Ljung R; Mannucci PM; Nicolaides K
    Bull World Health Organ; 1993; 71(3-4):429-58. PubMed ID: 8324863
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Molecular genetics and counselling in haemophilia.
    Peake I
    Thromb Haemost; 1995 Jul; 74(1):40-4. PubMed ID: 8578494
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Methods for the detection of haemophilia carriers: a memorandum.
    Bull World Health Organ; 1977; 55(6):675-702. PubMed ID: 304395
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A 6-year follow-up of dosing, coagulation factor levels and bleedings in relation to joint status in the prophylactic treatment of haemophilia.
    Ahnström J; Berntorp E; Lindvall K; Björkman S
    Haemophilia; 2004 Nov; 10(6):689-97. PubMed ID: 15569163
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Carrier detection and prenatal diagnosis in haemophilia A and B.
    Chistolini A; Papacchini M; Mazzucconi MG; La Verde G; Arcieri R; Ferrari A; Paesano R; Pachi A; Mariani G
    Haematologica; 1990; 75(5):424-8. PubMed ID: 1982946
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Treatment of hemophilia.
    Meili EO
    Schweiz Med Wochenschr Suppl; 1991; 43():82-9. PubMed ID: 1843043
    [No Abstract]   [Full Text] [Related]  

  • 9. Carrier detection and prenatal diagnosis in families with haemophilia.
    Shetty S; Ghosh K; Bhide A; Mohanty D
    Natl Med J India; 2001; 14(2):81-3. PubMed ID: 11396323
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Revision consensus hemophilia: treatment and responsibility. Nederlandse Vereniging van Hemophilia Patients].
    Briët E; Mauser-Bunschoten EP
    Ned Tijdschr Geneeskd; 1997 Dec; 141(52):2566-71. PubMed ID: 9555158
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Management of carriers and babies with haemophilia.
    Street AM; Ljung R; Lavery SA
    Haemophilia; 2008 Jul; 14 Suppl 3():181-7. PubMed ID: 18510540
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Haemophilia management in New Zealand: an Auckland perspective.
    Ockelford PA; Benny AG; Van de Water NS; Berry EW
    N Z Med J; 1989 Apr; 102(866):189-91. PubMed ID: 2496366
    [No Abstract]   [Full Text] [Related]  

  • 13. [Detection of Hemophilia A carrier state].
    Michalski R; Pniejnia-Olszyński W; Bykowska K; Lopaciuk S
    Acta Haematol Pol; 1977; 8(3):229-33. PubMed ID: 920063
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Partial deletions of factor VIII gene as molecular diagnostic markers in haemophilia A.
    Wehnert M; Herrmann FH; Wulff K
    Dis Markers; 1989; 7(2):113-7. PubMed ID: 2567219
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bleeding symptoms in carriers of hemophilia A and B.
    Mauser Bunschoten EP; van Houwelingen JC; Sjamsoedin Visser EJ; van Dijken PJ; Kok AJ; Sixma JJ
    Thromb Haemost; 1988 Jun; 59(3):349-52. PubMed ID: 2847347
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Relation of factor VIII and IX inhibitors with ABO blood groups in 150 patients with haemophilia A and B.
    Torghabeh HM; Pourfathollah A; Shooshtari MM; Yazdi ZR
    Iran J Allergy Asthma Immunol; 2006 Mar; 5(1):33-4. PubMed ID: 17242502
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Direct carrier detection for severe haemophilia A: application to families with no available affected male.
    Maugard C; Aguilar-Martinez P; Schved JF; Biron C; Gris JC; Demaille J; Claustres M
    Genet Couns; 1995; 6(2):109-12. PubMed ID: 7546452
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Genetic questions of hemophilia].
    Weissbach G; Lenk H
    Z Gesamte Inn Med; 1981 Jun; 36(11):363-70. PubMed ID: 6795839
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic diagnosis of haemophilia and other inherited bleeding disorders.
    Peyvandi F; Jayandharan G; Chandy M; Srivastava A; Nakaya SM; Johnson MJ; Thompson AR; Goodeve A; Garagiola I; Lavoretano S; Menegatti M; Palla R; Spreafico M; Tagliabue L; Asselta R; Duga S; Mannucci PM
    Haemophilia; 2006 Jul; 12 Suppl 3():82-9. PubMed ID: 16684001
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Effect of stanozolol on factors VIII and IX and serum aminotransferases in haemophilia.
    Greer IA; Greaves M; Madhok R; McLoughlin K; Porter N; Lowe GD; Preston FE; Forbes CD
    Thromb Haemost; 1985 Jun; 53(3):386-9. PubMed ID: 3931287
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.