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Journal Abstract Search

120 related items for PubMed ID: 18841297

  • 1.
    ; . PubMed ID:
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  • 3. Fibrinogen Nottingham II: a novel Bbeta Arg264gly substitution causing hypofibrinogenaemia.
    Hill MB, Brennan SO, Dear A, Strong J, Nejim T, Dolan G.
    Thromb Haemost; 2006 Sep; 96(3):378-80. PubMed ID: 16953282
    [No Abstract] [Full Text] [Related]

  • 4. Characterisation of Fibrinogen Oslo IV by electrospray mass spectrometry.
    Brennan SO, Ridgway H, Stormorken H, Brosstad F, George PM.
    Thromb Haemost; 1997 May; 77(5):1040-1. PubMed ID: 9184429
    [No Abstract] [Full Text] [Related]

  • 5. Two different fibrinogen gene mutations associated with bleeding in the same family (A αGly13Glu and γGly16Ser) and their impact on fibrin clot properties: fibrinogen Krakow II and Krakow III.
    Pietrys D, Balwierz W, Iwaniec T, Vorjohann S, Neerman-Arbez M, Undas A.
    Thromb Haemost; 2011 Sep; 106(3):558-60. PubMed ID: 21725578
    [No Abstract] [Full Text] [Related]

  • 6. Two novel mutations at contiguous codons in the fibrinogen Bbeta chain associated with hypofibrinogenaemia.
    Davis RL, May S, Chunilal S, Brennan SO.
    Thromb Haemost; 2009 May; 101(5):980-2. PubMed ID: 19404555
    [No Abstract] [Full Text] [Related]

  • 7. Fibrinogen Leipzig II (gamma351Gly-->Ser and gamma82Ala-->Gly): hypodysfibrinogenaemia due to two independent amino acid substitutions within the same polypeptide chain.
    Meyer M, Dietzel H, Kaetzel R, Schmidt D, Liebscher K, Brennan SO.
    Thromb Haemost; 2007 Oct; 98(4):903-5. PubMed ID: 17938819
    [No Abstract] [Full Text] [Related]

  • 8. A novel fibrinogen variant--Praha I: hypofibrinogenemia associated with gamma Gly351Ser substitution.
    Kotlín R, Chytilová M, Suttnar J, Salaj P, Riedel T, Santrůcek J, Klener P, Dyr JE.
    Eur J Haematol; 2007 May; 78(5):410-6. PubMed ID: 17331136
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  • 9. Fibrinogen Mannheim II: a novel gamma307 His-->Tyr substitution in the gammaD domain causes hypofibrinogenemia.
    Dear A, Dempfle CE, Brennan SO, Kirschstein W, George PM.
    J Thromb Haemost; 2004 Dec; 2(12):2194-9. PubMed ID: 15613026
    [Abstract] [Full Text] [Related]

  • 10. Simulated point mutations in the Aalpha-chain of human fibrinogen support a role of the alphaC domain in the stabilization of fibrin gel.
    Colafranceschi M, Papi M, Giuliani A, Amiconi G, Colosimo A.
    Pathophysiol Haemost Thromb; 2006 Dec; 35(6):417-27. PubMed ID: 17565234
    [Abstract] [Full Text] [Related]

  • 11. Abnormal fibrinogens with two structural defects.
    Matsuda M, Terukina S, Yoshida N, Yamazumi K, Maekawa H.
    Adv Exp Med Biol; 1990 Dec; 281():63-72. PubMed ID: 2102626
    [No Abstract] [Full Text] [Related]

  • 12. Fibrinogen Seoul (FGG Ala341Asp): a novel mutation associated with hypodysfibrinogenemia.
    Song KS, Park NJ, Choi JR, Doh HJ, Chung KH.
    Clin Appl Thromb Hemost; 2006 Jul; 12(3):338-43. PubMed ID: 16959688
    [Abstract] [Full Text] [Related]

  • 13. Proceedings: A new fibrinogen anomaly: fibrinogen Buenos Aires.
    Buraschi JA, Sack ES, Quiroga E, Hendler H.
    Thromb Diath Haemorrh; 1975 Nov 15; 34(2):570-1. PubMed ID: 1198458
    [No Abstract] [Full Text] [Related]

  • 14. Fibrinogen Montreal: a novel missense mutation (Aa D496N) associated with hypofibrinogenaemia.
    Sheen CR, Brennan SO, Jabado N, George PM.
    Thromb Haemost; 2006 Aug 15; 96(2):231-2. PubMed ID: 16894470
    [No Abstract] [Full Text] [Related]

  • 15. "Limited proteolysis," a new bleeding syndrome with circulating fibrinogen fragments.
    Oldham FB, Warner D, Kalmaz E, Hampton JW.
    J Lab Clin Med; 1971 Nov 15; 78(5):846. PubMed ID: 5128897
    [No Abstract] [Full Text] [Related]

  • 16. [Fibrinolysis in dysfibrinogenemia].
    Witt I.
    Hamostaseologie; 2002 May 15; 22(2):11-2. PubMed ID: 12193971
    [No Abstract] [Full Text] [Related]

  • 17. Fibrinogen Krakow: a novel hypo/dysfibrinogenemia mutation in fibrinogen gamma chain (Asn325Ile) affecting fibrin clot structure and function.
    Undas A, Zdziarska J, Iwaniec T, Stepien E, Skotnicki AB, de Moerloose P, Neerman-Arbez M.
    Thromb Haemost; 2009 May 15; 101(5):975-6. PubMed ID: 19404553
    [No Abstract] [Full Text] [Related]

  • 18. Rare inherited disorders of fibrinogen.
    Acharya SS, Dimichele DM.
    Haemophilia; 2008 Nov 15; 14(6):1151-8. PubMed ID: 19141154
    [Abstract] [Full Text] [Related]

  • 19. Defective fibrinogen polymerization associated with a novel gamma279Ala-->Asp mutation.
    Brennan SO, Wyatt JM, Ockelford P, George PM.
    Br J Haematol; 2000 Feb 15; 108(2):236-40. PubMed ID: 10691848
    [Abstract] [Full Text] [Related]

  • 20. Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiency.
    Spena S, Asselta R, Caccia S, Rimoldi V, Giacomelli SH, Tagliaferri A, Peyvandi F, Castaman G, Duga S.
    Thromb Haemost; 2009 Sep 15; 102(3):603-6. PubMed ID: 19718484
    [No Abstract] [Full Text] [Related]

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