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Journal Abstract Search

135 related items for PubMed ID: 2133234

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  • 2. Fibrinogen Oviedo I. A new Spanish dysfibrinogenaemia.
    Fernández FJ, Rodríguez Pinto C, Páramo J, Cuesta B, Collado M, Rocha E.
    Blood Coagul Fibrinolysis; 1990 Oct; 1(4-5):571-5. PubMed ID: 2133236
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  • 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
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  • 6. Fibrinogen Stony Brook II: partial characterization of a heterozygously transmitted peptide A anomaly.
    Galanakis DK, Hultin M.
    Blood Coagul Fibrinolysis; 1990 Oct; 1(4-5):567-70. PubMed ID: 2133235
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  • 7. Fibrinogen Milano V: a congenital dysfibrinogenaemia with a gamma 275 Arg-->Cys substitution.
    Steinmann C, Bögli C, Jungo M, Lämmle B, Heinemann G, Wermuth B, Redaelli R, Baudo F, Furlan M.
    Blood Coagul Fibrinolysis; 1994 Aug; 5(4):463-71. PubMed ID: 7841300
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  • 12. Fibrinogen Philadelphia, a hypodysfibrinogenemia characterized by abnormal polymerization and fibrinogen hypercatabolism due to gamma S378P mutation.
    Keller MA, Martinez J, Baradet TC, Nagaswami C, Chernysh IN, Borowski MK, Surrey S, Weisel JW.
    Blood; 2005 Apr 15; 105(8):3162-8. PubMed ID: 15632207
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  • 13. 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 15; 134(4):901-8. PubMed ID: 25074738
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  • 15. Three cases of congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation in fibrinogen alpha chain Argl6His.
    Luo M, Deng D, Xiang L, Cheng P, Liao L, Deng X, Yan J, Lin F.
    Medicine (Baltimore); 2016 Sep 15; 95(39):e4864. PubMed ID: 27684817
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  • 17. A hereditary dysfibrinogenemia: fibrinogen Awaji.
    Matsuo T, Okuno S, Mukaida T, Ueshima S, Okada K, Matsuo O.
    Haemostasis; 1987 Sep 15; 17(1-2):89-97. PubMed ID: 3596361
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  • 18. Fibrinogen Poissy II (gammaN361K): a novel dysfibrinogenemia associated with defective polymerization and peptide B release.
    Mathonnet F, Guillon L, Detruit H, Mazmanian GM, Dreyfus M, Alvarez JC, Giudicelli Y, de Mazancourt P.
    Blood Coagul Fibrinolysis; 2003 Apr 15; 14(3):293-8. PubMed ID: 12695754
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