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Journal Abstract Search

121 related items for PubMed ID: 28537987

  • 1. Congenital dysfibrinogenemia in a Japanese family with fibrinogen Naples (BβAla68Thr) manifesting as superior sagittal sinus thrombosis.
    Yoshida S, Kibe T, Matsubara R, Koizumi SI, Nara K, Amano K, Okumura N.
    Blood Coagul Fibrinolysis; 2017 Oct; 28(7):580-584. PubMed ID: 28537987
    [Abstract] [Full Text] [Related]

  • 2. Heterozygous FGA p.Asp473Ter (fibrinogen Nieuwegein) presenting as antepartum cerebral thrombosis.
    Tajdar M, Orlando C, Casini A, Herpol M, De Bisschop B, Govaert P, Neerman-Arbez M, Jochmans K.
    Thromb Res; 2018 Mar; 163():185-189. PubMed ID: 29122299
    [Abstract] [Full Text] [Related]

  • 3. Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen.
    Haverkate F, Samama M.
    Thromb Haemost; 1995 Jan; 73(1):151-61. PubMed ID: 7740487
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  • 4. Fibrinogen Šumperk II: dysfibrinogenemia in an individual with two coding mutations.
    Kotlín R, Suttnar J, Cápová I, Hrachovinová I, Urbánková M, Dyr JE.
    Am J Hematol; 2012 May; 87(5):555-7. PubMed ID: 22407772
    [Abstract] [Full Text] [Related]

  • 5. Congenital fibrinogen disorders with repeated thrombosis.
    Zhang X, Zhang C, Wang B, Chen N, Sun G, Guo X.
    J Thromb Thrombolysis; 2020 Feb; 49(2):312-315. PubMed ID: 31542854
    [Abstract] [Full Text] [Related]

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  • 7. The dilemma of inherited dysfibrinogenemia during pregnancy.
    Munoz J, Schering J, Lambing A, Neal S, Goyert G, Green PM, Hanbali A, Raman S, Kuriakose P.
    Blood Coagul Fibrinolysis; 2012 Dec; 23(8):775-7. PubMed ID: 23135383
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  • 9. A novel Asp344Val substitution in the fibrinogen gamma chain (fibrinogen Caen) causes dysfibrinogenemia associated with thrombosis.
    Robert-Ebadi H, Le Querrec A, de Moerloose P, Gandon-Laloum S, Borel Derlon A, Neerman-Arbez M.
    Blood Coagul Fibrinolysis; 2008 Oct; 19(7):697-9. PubMed ID: 18832913
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  • 11. Fibrinogen Nový Jicín and Praha II: cases of hereditary Aalpha 16 Arg-->Cys and Aalpha 16 Arg-->His dysfibrinogenemia.
    Kotlín R, Chytilová M, Suttnar J, Riedel T, Salaj P, Blatný J, Santrůcek J, Klener P, Dyr JE.
    Thromb Res; 2007 Oct; 121(1):75-84. PubMed ID: 17408725
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  • 12. Paradoxical bleeding and thrombosis in a patient with afibrinogenemia and fibrinogen Mumbai mutation.
    Mukaddam A, Patil R, Jadli A, Chandrakala S, Ghosh K, Shetty S.
    Am J Clin Pathol; 2015 May; 143(5):755-7. PubMed ID: 25873512
    [Abstract] [Full Text] [Related]

  • 13. Diagnosis of congenital fibrinogen disorders.
    Lebreton A, Casini A.
    Ann Biol Clin (Paris); 2016 Aug 01; 74(4):405-12. PubMed ID: 27492693
    [Abstract] [Full Text] [Related]

  • 14. Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management.
    Casini A, Neerman-Arbez M, Ariëns RA, de Moerloose P.
    J Thromb Haemost; 2015 Jun 01; 13(6):909-19. PubMed ID: 25816717
    [Abstract] [Full Text] [Related]

  • 15. Reversible non-thrombotic occlusion of the superior sagittal sinus caused by metastatic malignant lymphoma--case report.
    Matsumoto K, Ohta M, Takeshita I.
    Neurol Med Chir (Tokyo); 2003 Jul 01; 43(7):349-51. PubMed ID: 12924595
    [Abstract] [Full Text] [Related]

  • 16. Severe congenital dysfibrinogenemia (fibrinogen-Riyadh): a family study.
    al-Fawaz IM, Gader AM.
    Acta Haematol; 1992 Jul 01; 88(4):194-7. PubMed ID: 1292308
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  • 18. Two novel mutations in the fibrinogen γ nodule.
    Kotlín R, Pastva O, Stikarová J, Hlaváčková A, Suttnar J, Chrastinová L, Riedel T, Salaj P, Dyr JE.
    Thromb Res; 2014 Oct 01; 134(4):901-8. PubMed ID: 25074738
    [Abstract] [Full Text] [Related]

  • 19. Dusart Syndrome in a Scandinavian family characterized by arterial and venous thrombosis at young age.
    Ramanathan R, Gram J, Feddersen S, Nybo M, Larsen A, Sidelmann JJ.
    Scand J Clin Lab Invest; 2013 Oct 01; 73(7):585-90. PubMed ID: 24000886
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