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Journal Abstract Search

79 related items for PubMed ID: 367661

  • 1. Congenital abnormalities of fibrinogen.
    Beck EA.
    Clin Haematol; 1979 Feb; 8(1):169-81. PubMed ID: 367661
    [No Abstract] [Full Text] [Related]

  • 2. Mutation of the translation initiation codon in FGA causes congenital afibrinogenemia.
    Tirefort Y, Alson OR, de Moerloose P, Neerman-Arbez M.
    Blood Coagul Fibrinolysis; 2012 Sep; 23(6):556-8. PubMed ID: 22732251
    [Abstract] [Full Text] [Related]

  • 3. Congenital afibrinogenemia in Hasan Sadikin Hospital.
    Supandiman I, Sumantri R.
    Southeast Asian J Trop Med Public Health; 1993 Sep; 24 Suppl 1():267-9. PubMed ID: 7886594
    [Abstract] [Full Text] [Related]

  • 4. Congenital dysfibrinogenemias. A review.
    Rocha E, Páramo JA, Aranda A, Cuesta B, Fernández J.
    Ric Clin Lab; 1985 Sep; 15(3):205-29. PubMed ID: 3909359
    [Abstract] [Full Text] [Related]

  • 5. [Afibrinogenemia and dysfibrinogenemia].
    Fukui H.
    Nihon Rinsho; 1970 Aug; 28(8):2086-91. PubMed ID: 4917925
    [No Abstract] [Full Text] [Related]

  • 6. [Congenital afibrinogenemia with bleeding, bone cysts and antibodies to fibrinogen].
    Ra'anani P, Levi Y, Varon D, Gitel S, Martinowitz U.
    Harefuah; 1991 Nov 01; 121(9):291-3. PubMed ID: 1800275
    [Abstract] [Full Text] [Related]

  • 7. Congenital disorders of fibrinogen.
    Agarwal MB, Sanzgiri PS, Bhanotra PC, Rao S, Mehta BC, Shah MD.
    J Postgrad Med; 1981 Jul 01; 27(3):178-83. PubMed ID: 7299708
    [No Abstract] [Full Text] [Related]

  • 8. Fibrinogen Vicenza and Genova II: two new cases of congenital dysfibrinogenemia with isolated defect of fibrin monomer polymerization and inhibitory activity on normal coagulation.
    Rodeghiero F, Castaman GC, Dal Belin Peruffo A, Dini E, Galletti A, Barone E, Gastaldi G.
    Thromb Haemost; 1987 Jun 03; 57(3):252-8. PubMed ID: 2958952
    [Abstract] [Full Text] [Related]

  • 9. [Congenital dysfibrinogenemia and thrombosis].
    Matsuo T.
    Rinsho Byori; 1987 May 03; 35(5):493-6. PubMed ID: 3302409
    [No Abstract] [Full Text] [Related]

  • 10. Dysfibrinogenemia. A current perspective.
    Galanakis DK.
    Clin Lab Med; 1984 Jun 03; 4(2):395-418. PubMed ID: 6388985
    [Abstract] [Full Text] [Related]

  • 11. Fibrinogen--its role in platelet agglutination and agglutinate stability. A study of congenital aibrinogenemia.
    Rodman NF, Mason RG, Painter JC, Brinkhous KM.
    Lab Invest; 1966 Mar 03; 15(3):641-56. PubMed ID: 5932939
    [No Abstract] [Full Text] [Related]

  • 12. Mesenteric venous thrombosis in a patient with congenital afibrinogenemia and diffuse peritonitis.
    Takasugi Y, Shiokawa Y, Kajikawa R, Oh J, Yamamoto Y, Sakata I, Koga Y.
    Ann Hematol; 2005 Feb 03; 84(2):129-30. PubMed ID: 15503018
    [No Abstract] [Full Text] [Related]

  • 13. Retrochorionic hematoma in congenital afibrinogenemia: resolution with fibrinogen concentrate infusions.
    Aygören-Pürsün E, Martinez Saguer I, Rusicke E, Louwen F, Geka F, Ivaskevicius V, Oldenburg J, Klingebiel T, Kreuz W.
    Am J Hematol; 2007 Apr 03; 82(4):317-20. PubMed ID: 17034026
    [Abstract] [Full Text] [Related]

  • 14. [Clinical aspects and clinical course of a case of congenital hypofibrinogenemia].
    Kruse H, Schulz K, Blau HJ.
    Kinderarztl Prax; 1969 Aug 03; 37(8):361-72. PubMed ID: 5355994
    [No Abstract] [Full Text] [Related]

  • 15. [Massive hemoperitoneum caused by rupture of the spleen, a complication of congenital afibrinogenemia. Conservative treatment].
    Gallet S, Tran Minh V, Louis D, Cotton JB, Berthier JC, Hartemann E.
    Pediatrie; 1985 Aug 03; 40(5):385-91. PubMed ID: 3909095
    [Abstract] [Full Text] [Related]

  • 16. Spontaneous extra-axial intracranial hemorrhage followed by thrombosis in congenital afibrinogenemia: perioperative management of this rare combination.
    Pati S, Kombogiorgas D, Anwar A, Price RF.
    Surg Neurol; 2009 Jun 03; 71(6):689-92, discussion 692. PubMed ID: 18295846
    [Abstract] [Full Text] [Related]

  • 17. Afibrinogenemia resulting from homozygous nonsense mutation in A alpha chain gene associated with multiple thrombotic episodes.
    Simsek I, de Mazancourt P, Horellou MH, Erdem H, Pay S, Dinc A, Samama MM.
    Blood Coagul Fibrinolysis; 2008 Apr 03; 19(3):247-53. PubMed ID: 18388508
    [Abstract] [Full Text] [Related]

  • 18. [Fibrinogen beta chain gene mutation contributes to one congenital afibrinogenemia].
    Xu XC, Zhou RF, Wu JS, Fang Y, Wang XF, Zhai ZM, Wang HL.
    Zhonghua Xue Ye Xue Za Zhi; 2005 Mar 03; 26(3):137-9. PubMed ID: 15946523
    [Abstract] [Full Text] [Related]

  • 19. Congenital fibrinogen disorders.
    de Moerloose P, Neerman-Arbez M.
    Semin Thromb Hemost; 2009 Jun 03; 35(4):356-66. PubMed ID: 19598064
    [Abstract] [Full Text] [Related]

  • 20. A new congenital abnormality of human fibrinogen. Fibrinogen Bethesda II.
    Gralnick HR, Givelber HM, Finlayson JS.
    Thromb Diath Haemorrh; 1973 Jun 28; 29(3):562-71. PubMed ID: 4761824
    [No Abstract] [Full Text] [Related]

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