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Journal Abstract Search

273 related items for PubMed ID: 16607083

  • 1. Novel fibrinogen mutation (gamma 313 Ser-->Asn) associated with hypofibrinogenemia in two unrelated families.
    Meyer M, Bergmann F, Brennan SO.
    Blood Coagul Fibrinolysis; 2006 Jan; 17(1):63-7. PubMed ID: 16607083
    [Abstract] [Full Text] [Related]

  • 2. Hypofibrinogenemia due to novel 316 Asp --> Tyr substitution in the fibrinogen Bbeta chain.
    Brennan SO, Wyatt JM, May S, De Caigney S, George PM.
    Thromb Haemost; 2001 Mar; 85(3):450-3. PubMed ID: 11307813
    [Abstract] [Full Text] [Related]

  • 3. Fibrinogen St. Gallen I (gamma 292 Gly--> Val): evidence for structural alterations causing defective polymerization and fibrinogenolysis.
    Stucki B, Schmutz P, Schmid L, Haeberli A, Lämmle B, Furlan M.
    Thromb Haemost; 1999 Feb; 81(2):268-74. PubMed ID: 10064005
    [Abstract] [Full Text] [Related]

  • 4. A C-terminal amino acid substitution in the gamma-chain caused by a novel heterozygous frameshift mutation (Fibrinogen Matsumoto VII) results in hypofibrinogenaemia.
    Fujihara N, Haneishi A, Yamauchi K, Terasawa F, Ito T, Ishida F, Okumura N.
    Thromb Haemost; 2010 Aug; 104(2):213-23. PubMed ID: 20589319
    [Abstract] [Full Text] [Related]

  • 5. Novel fibrinogen gamma375 Arg-->Trp mutation (fibrinogen aguadilla) causes hepatic endoplasmic reticulum storage and hypofibrinogenemia.
    Brennan SO, Maghzal G, Shneider BL, Gordon R, Magid MS, George PM.
    Hepatology; 2002 Sep; 36(3):652-8. PubMed ID: 12198657
    [Abstract] [Full Text] [Related]

  • 6. Fibrinogen Saint-Germain II: hypofibrinogenemia due to heterozygous gamma N345S mutation.
    de Raucourt E, de Mazancourt P, Maghzal GJ, Brennan SO, Mosesson MW.
    Thromb Haemost; 2005 Nov; 94(5):965-8. PubMed ID: 16363237
    [Abstract] [Full Text] [Related]

  • 7. Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutations.
    Castaman G, Giacomelli SH, Duga S, Rodeghiero F.
    Haemophilia; 2008 May; 14(3):630-3. PubMed ID: 18393984
    [No Abstract] [Full Text] [Related]

  • 8. A case of congenital afibrinogenemia: fibrinogen Hakata, a novel nonsense mutation of the fibrinogen gamma-chain gene.
    Iida H, Ishii E, Nakahara M, Urata M, Wakiyama M, Kurihara M, Watanabe K, Kai T, Ihara K, Kinoshita S, Hamasaki N.
    Thromb Haemost; 2000 Jul; 84(1):49-53. PubMed ID: 10928469
    [Abstract] [Full Text] [Related]

  • 9. Congenital hypofibrinogenemia: characterization of two missense mutations affecting fibrinogen assembly and secretion.
    Platè M, Asselta R, Spena S, Spreafico M, Fagoonee S, Peyvandi F, Tenchini ML, Duga S.
    Blood Cells Mol Dis; 2008 Jul; 41(3):292-7. PubMed ID: 18676163
    [Abstract] [Full Text] [Related]

  • 10. Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia.
    Asselta R, Spena S, Duga S, Peyvandi F, Malcovati M, Mannucci PM, Tenchini ML.
    Haematologica; 2002 Aug; 87(8):855-9. PubMed ID: 12161363
    [Abstract] [Full Text] [Related]

  • 11. A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo.
    Margaglione M, Vecchione G, Santacroce R, D'Angelo F, Casetta B, Papa ML, Grandone E, Di Minno G.
    Thromb Haemost; 2001 Dec; 86(6):1483-8. PubMed ID: 11776317
    [Abstract] [Full Text] [Related]

  • 12. Paris I dysfibrinogenemia: a point mutation in intron 8 results in insertion of a 15 amino acid sequence in the fibrinogen gamma-chain.
    Rosenberg JB, Newman PJ, Mosesson MW, Guillin MC, Amrani DL.
    Thromb Haemost; 1993 Mar 01; 69(3):217-20. PubMed ID: 8470043
    [Abstract] [Full Text] [Related]

  • 13. A novel fibrinogen variant--Liberec: dysfibrinogenaemia associated with gamma Tyr262Cys substitution.
    Kotlín R, Sobotková A, Suttnar J, Salaj P, Walterová L, Riedel T, Reicheltová Z, Dyr JE.
    Eur J Haematol; 2008 Aug 01; 81(2):123-9. PubMed ID: 18485115
    [Abstract] [Full Text] [Related]

  • 14. Hepatic fibrinogen storage disease: identification of two novel mutations (p.Asp316Asn, fibrinogen Pisa and p.Gly366Ser, fibrinogen Beograd) impacting on the fibrinogen γ-module.
    Asselta R, Robusto M, Braidotti P, Peyvandi F, Nastasio S, D'Antiga L, Perisic VN, Maggiore G, Caccia S, Duga S.
    J Thromb Haemost; 2015 Aug 01; 13(8):1459-67. PubMed ID: 26039544
    [Abstract] [Full Text] [Related]

  • 15. Fibrinogen Bastia (gamma 318 Asp-->Tyr) a novel abnormal fibrinogen characterized by defective fibrin polymerization.
    Lounes KC, Soria C, Valognes A, Turchini MF, Soria J, Koopman J.
    Thromb Haemost; 1999 Dec 01; 82(6):1639-43. PubMed ID: 10613648
    [Abstract] [Full Text] [Related]

  • 16. 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 01; 19(7):697-9. PubMed ID: 18832913
    [Abstract] [Full Text] [Related]

  • 17. Gene analyses of abnormal fibrinogens with a mutation in the gamma chain.
    Mimuro J, Muramatsu S, Maekawa H, Sakata Y, Kaneko M, Yoshitake S, Okuma M, Ito Y, Takeda Y, Matsuda M.
    Int J Hematol; 1992 Oct 01; 56(2):129-34. PubMed ID: 1421174
    [Abstract] [Full Text] [Related]

  • 18. Severe bleeding and miscarriages in a hypofibrinogenemic woman heterozygous for the gamma Ala82Gly mutation.
    Zdziarska J, Undas A, Basa J, Iwaniec T, Skotnicki AB, de Moerloose P, Neerman-Arbez M.
    Blood Coagul Fibrinolysis; 2009 Jul 01; 20(5):374-6. PubMed ID: 19300242
    [Abstract] [Full Text] [Related]

  • 19. 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 01; 12(3):338-43. PubMed ID: 16959688
    [Abstract] [Full Text] [Related]

  • 20. Hypofibrinogenaemia associated with a novel heterozygous gamma289 Ala -->Val substitution (fibrinogen Dorfen).
    Dear A, Brennan SO, Dempfle CE, Kirschstein W, George PM.
    Thromb Haemost; 2004 Dec 01; 92(6):1291-5. PubMed ID: 15583736
    [Abstract] [Full Text] [Related]

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