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Journal Abstract Search

203 related items for 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
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  • 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
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  • 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
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  • 5. Methods for the detection of haemophilia carriers: a memorandum.
    Bull World Health Organ; 1977 Mar; 55(6):675-702. PubMed ID: 304395
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  • 8. Treatment of hemophilia.
    Meili EO.
    Schweiz Med Wochenschr Suppl; 1991 Mar; 43():82-9. PubMed ID: 1843043
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  • 10. [Revision consensus hemophilia: treatment and responsibility. Nederlandse Vereniging van Hemophilia Patients].
    Briët E, Mauser-Bunschoten EP.
    Ned Tijdschr Geneeskd; 1997 Dec 27; 141(52):2566-71. PubMed ID: 9555158
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  • 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 26; 102(866):189-91. PubMed ID: 2496366
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  • 14. Partial deletions of factor VIII gene as molecular diagnostic markers in haemophilia A.
    Wehnert M, Herrmann FH, Wulff K.
    Dis Markers; 1989 Apr 26; 7(2):113-7. PubMed ID: 2567219
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  • 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 16; 59(3):349-52. PubMed ID: 2847347
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  • 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 Jun 16; 6(2):109-12. PubMed ID: 7546452
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  • 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 16; 12 Suppl 3():82-9. PubMed ID: 16684001
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  • 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 24; 53(3):386-9. PubMed ID: 3931287
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