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Pubmed for Handhelds

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Journal Abstract Search

295 related items for PubMed ID: 8470043

  • 21. Genetic analyses of novel compound heterozygous hypodysfibrinogenemia, Tsukuba I: FGG c.1129+62_65 del AATA and FGG c.1299+4 del A.
    Mukai S, Nagata K, Ikeda M, Arai S, Sugano M, Honda T, Okumura N.
    Thromb Res; 2016 Dec; 148():111-117. PubMed ID: 27837696
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  • 22. Novel fibrinogen Aalpha chain mutation associated with afibrinogenaemia.
    Saravanan L, Brennan S, George P, Lowen R, Kirkland M, Campbell P.
    Pathology; 2007 Oct; 39(5):519-20. PubMed ID: 17886104
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  • 23. 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; 14(3):293-8. PubMed ID: 12695754
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  • 30. A novel fibrinogen variant: dysfibrinogenemia associated with γAsp185Asn substitution.
    Zhou N, Xu P, Zhou M, Xu Y, Li P, Chen B, Ouyang J, Zhou R.
    J Thromb Thrombolysis; 2017 Jul; 44(1):139-144. PubMed ID: 28425010
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  • 31. [A case of dysfibrinogenemia without hemorrhagic diathesis or thromboembolism linked to a new mutation p.H103N in fibrinogen γ chain].
    Devignes J, Hanss M, Chabaud A, Toussaint-Hacquard M, Mansuy L, De Mazancourt P, Lecompte T.
    Ann Biol Clin (Paris); 2013 Jul; 71(4):489-95. PubMed ID: 23906582
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  • 35. Hypofibrinogenemia in an individual with 2 coding (gamma82 A-->G and Bbeta235 P-->L) and 2 noncoding mutations.
    Brennan SO, Fellowes AP, Faed JM, George PM.
    Blood; 2000 Mar 01; 95(5):1709-13. PubMed ID: 10688828
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