These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

419 related items for PubMed ID: 18388508

  • 21. Pseudo-exon activation caused by a deep-intronic mutation in the fibrinogen gamma-chain gene as a novel mechanism for congenital afibrinogenaemia.
    Spena S, Asselta R, Platé M, Castaman G, Duga S, Tenchini ML.
    Br J Haematol; 2007 Oct; 139(1):128-32. PubMed ID: 17854317
    [Abstract] [Full Text] [Related]

  • 22. 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]

  • 23. Identification of three FGA mutations in two Chinese families with congenital afibrinogenaemia.
    Fang Y, Dai BT, Wang XF, Fu QH, Dai J, Xie F, Cai XH, Wang HL, Wang ZY.
    Haemophilia; 2006 Nov; 12(6):615-20. PubMed ID: 17083511
    [Abstract] [Full Text] [Related]

  • 24. A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing.
    Margaglione M, Santacroce R, Colaizzo D, Seripa D, Vecchione G, Lupone MR, De Lucia D, Fortina P, Grandone E, Perricone C, Di Minno G.
    Blood; 2000 Oct 01; 96(7):2501-5. PubMed ID: 11001903
    [Abstract] [Full Text] [Related]

  • 25. Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia.
    Vu D, Di Sanza C, Caille D, de Moerloose P, Scheib H, Meda P, Neerman-Arbez M.
    Hum Mol Genet; 2005 Nov 01; 14(21):3271-80. PubMed ID: 16195396
    [Abstract] [Full Text] [Related]

  • 26. [Inherited dysfibrinogenemia caused by Arg275His in the beta chain of fibrinogen].
    Fang Y, Wang X, Qi H, Wu W, Ding Q, Dai J, Zhou R, Wang W, Xie S, Wang H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr 01; 22(2):201-3. PubMed ID: 15793786
    [Abstract] [Full Text] [Related]

  • 27. Deletion of the fibrinogen [correction of fibrogen] alpha-chain gene (FGA) causes congenital afibrogenemia.
    Neerman-Arbez M, Honsberger A, Antonarakis SE, Morris MA.
    J Clin Invest; 1999 Jan 01; 103(2):215-8. PubMed ID: 9916133
    [Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29. Maternal chromosome 4 heterodisomy/isodisomy and Bβ chain Trp323X mutation resulting in severe hypodysfibrinogenaemia.
    Ding Q, Ouyang Q, Xi X, Wang X, Shen Y, Wang H.
    Thromb Haemost; 2012 Oct 01; 108(4):654-61. PubMed ID: 22955321
    [Abstract] [Full Text] [Related]

  • 30. 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]

  • 31. Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group.
    Santacroce R, Cappucci F, Pisanelli D, Perricone F, Papa ML, Santoro R, Grandone E, Margaglione M.
    Blood Coagul Fibrinolysis; 2006 Jun 01; 17(4):235-40. PubMed ID: 16651864
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. [Congenital afibrinogenemia caused by a novel insertion mutation in the FGB gene].
    Zhang J, Zhao XJ, Wang ZY, Yu ZQ, Cao LJ, Ma ZN, Zhang J, Zhang W, Bai X, Ruan CG.
    Zhonghua Xue Ye Xue Za Zhi; 2013 Sep 01; 34(9):751-6. PubMed ID: 24103871
    [Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. [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 Sep 01; 71(4):489-95. PubMed ID: 23906582
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 21.