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 *

63 related articles for article (PubMed ID: 505387)

  • 21. [With regard to a double factor XI/XII deficiency].
    Tortosa Cavero JI
    Sangre (Barc); 1992 Aug; 37(4):304-5. PubMed ID: 1514151
    [No Abstract]   [Full Text] [Related]  

  • 22. Hemophilia A in a phenotypic female with normal male karyotype associated with a low factor XII level.
    Huisse MG; de Grouchy J; Menaché D; de Crépy B; Andreassian B; Baumann J
    Ann Genet; 1980; 23(1):31-4. PubMed ID: 6965837
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Haemophilia B in a female caused by skewed inactivation of the normal X-chromosome.
    Espinós C; Lorenzo JI; Casaña P; Martínez F; Aznar JA
    Haematologica; 2000 Oct; 85(10):1092-5. PubMed ID: 11025603
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Hemophilia A and hemophilia B in a family of French bulldogs.
    Slappendel RJ
    Tijdschr Diergeneeskd; 1975 Oct; 100(20):1075-88. PubMed ID: 1209580
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Factor XII deficiency and pregnancy.
    Lao TT; Lewinsky RM; Ohlsson A; Cohen H
    Obstet Gynecol; 1991 Sep; 78(3 Pt 2):491-3. PubMed ID: 1870803
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [3 families with a congenital factor X deficiency, one of them with an associated factor XII deficiency].
    Pérez Sánchez M; López J; López JL; Haya S; Lavilla E; Cárdenas MC; Rey L; Gómez N; Fernández-Rañada JM
    Sangre (Barc); 1993 Feb; 38(1):57-61. PubMed ID: 8470037
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Colour vision deficiencies and haemophilia.
    Jaeger W; Schneider VJ
    Mod Probl Ophthalmol; 1976; 17():143-6. PubMed ID: 1085859
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The life-long haemorrhagic disorders with prolonged bleeding time and factor-IX deficiency.
    Dube B; Gupta SP; Udupa KN; Somani PN; Srivastava PK; Kubey SM
    J Assoc Physicians India; 1973 Jun; 21(6):523-7. PubMed ID: 4792727
    [No Abstract]   [Full Text] [Related]  

  • 29. Hereditary Hageman factor (factor XII) deficiency: report of three families and review of the literature published in Japan.
    Sano M; Saito H; Sugihara T; Suzuki H; Kojima T; Shirakawa M; Kamiya T; Ohya I
    Nihon Ketsueki Gakkai Zasshi; 1986 Sep; 49(6):1275-81. PubMed ID: 3811790
    [No Abstract]   [Full Text] [Related]  

  • 30. Factor XII deficiency and von Willebrand's disease in a family of miniature poodle dogs.
    Randolph JF; Center SA; Dodds WJ
    Cornell Vet; 1986 Jan; 76(1):3-10. PubMed ID: 3484442
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Hemophilia B carrier determination based on family-specific mutation detection by DNA single-strand conformation analysis.
    Poon MC; Anand S; Fraser BM; Hoar DI; Sinclair GD
    J Lab Clin Med; 1993 Jul; 122(1):55-63. PubMed ID: 8320491
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Spectrum of hereditary coagulation factor deficiencies in eastern province, Saudi Arabia.
    Islam SI; Quadri MI
    East Mediterr Health J; 1999 Nov; 5(6):1188-95. PubMed ID: 11924110
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Congenital factor XII deficiency: successful open heart surgery and anticoagulation.
    Kelsey PR; Bottomley J; Grotte GJ; Maciver JE
    Clin Lab Haematol; 1985; 7(4):379-81. PubMed ID: 3879475
    [No Abstract]   [Full Text] [Related]  

  • 34. [Microspherocytosis associated with factor IX deficiency].
    Thouverez JP; Coeur P; Bryon PA; Revol L; Croizat P
    Sem Hop; 1970 Feb; 46(9):621-2. PubMed ID: 4314358
    [No Abstract]   [Full Text] [Related]  

  • 35. Two distinct mutations cause severe hemophilia B in two unrelated canine pedigrees.
    Gu W; Brooks M; Catalfamo J; Ray J; Ray K
    Thromb Haemost; 1999 Oct; 82(4):1270-5. PubMed ID: 10544912
    [TBL] [Abstract][Full Text] [Related]  

  • 36. DNA analysis of seven patients with hemophilia B who have anti-factor IX antibodies: relationship to clinical manifestations and evidence that the abnormal gene was inherited.
    Tanimoto M; Kojima T; Kamiya T; Takamatsu J; Ogata K; Obata Y; Inagaki M; Iizuka A; Nagao T; Kurachi K
    J Lab Clin Med; 1988 Sep; 112(3):307-13. PubMed ID: 3411192
    [TBL] [Abstract][Full Text] [Related]  

  • 37. An unusual complication in a gravida with factor IX deficiency: case report with review of the literature.
    Guy GP; Baxi LV; Hurlet-Jensen A; Chao CR
    Obstet Gynecol; 1992 Sep; 80(3 Pt 2):502-5. PubMed ID: 1495722
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [The genetics of factor XII deficiency].
    Kempter B; Rüth S; Epple I; Lohse P
    Beitr Infusionsther; 1993; 31():174-8. PubMed ID: 7693250
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Presence of inactive factor ix in variants of hemophilia, type B, and in carriers of hemophilia B].
    Elodi S
    Minerva Med; 1975 Jun; 66(42):2037-43. PubMed ID: 1138213
    [No Abstract]   [Full Text] [Related]  

  • 40. [Use of chromogenic substrates in the clarification of disorders in the early stages of blood coagulation].
    Vogel G; Stürzebecher J; Klessen C; Lauten G
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1982; 109(1):115-20. PubMed ID: 6177592
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.