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Journal Abstract Search

202 related items for PubMed ID: 17604827

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  • 22. Exon skipping and aberrant signal peptide cleavage produce novel fibrinogen with an Aα chain lacking the first 42 residues.
    Brennan SO, Laurie AD, McRae S.
    Thromb Haemost; 2016 Aug 30; 116(3):581-5. PubMed ID: 27277572
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  • 24. A new heterozygous mutation in gamma fibrinogen gene leading to 326 Cys-->Ser substitution in fibrinogen Córdoba is associated with defective polymerization and familial hypodysfibrinogenemia.
    Guglielmone HA, Sanchez MC, Abate Daga D, Bocco JL.
    J Thromb Haemost; 2004 Feb 30; 2(2):352-4. PubMed ID: 14996011
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  • 29. 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 30; 81(2):123-9. PubMed ID: 18485115
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  • 30. 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 Aug 30; 121(1):75-84. PubMed ID: 17408725
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  • 32. The amplitude of coagulation curves from thrombin time tests allows dysfibrinogenemia caused by the common mutation FGG-Arg301 to be distinguished from hypofibrinogenemia.
    Jacquemin M, Vanlinthout I, Van Horenbeeck I, Debasse M, Toelen J, Schoeters J, Lavend'homme R, Freson K, Peerlinck K.
    Int J Lab Hematol; 2017 Jun 30; 39(3):301-307. PubMed ID: 28318107
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  • 33. Fibrinogen Claro--another dysfunctional fibrinogen variant with gamma 275 arginine-->histidine substitution.
    Steinmann C, Jungo M, Beck EA, Lämmle B, Furlan M.
    Thromb Res; 1996 Jan 01; 81(1):145-50. PubMed ID: 8747529
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  • 35. Fibrinogen Matsumoto II: gamma 308 Asn-->Lys (AAT-->AAG) mutation associated with bleeding tendency.
    Okumura N, Furihata K, Terasawa F, Ishikawa S, Ueno I, Katsuyama T.
    Br J Haematol; 1996 Sep 01; 94(3):526-8. PubMed ID: 8790154
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  • 37. Novel homozygous fibrinogen Aα chain truncation causes severe afibrinogenemia with life threatening complications in a two-year-old boy.
    Stikarová J, Blatný J, Kotlín R, Suttnar J, Zapletal O, Pimková K, Májek P, Hrachovinová I, Dyr JE.
    Thromb Res; 2013 Oct 01; 132(4):490-2. PubMed ID: 24050829
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