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

217 related items for PubMed ID: 12511408

  • 1. Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family.
    Neerman-Arbez M, Vu D, Abu-Libdeh B, Bouchardy I, Morris MA.
    Blood; 2003 May 01; 101(9):3492-4. PubMed ID: 12511408
    [Abstract] [Full Text] [Related]

  • 2. Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion.
    Vu D, Bolton-Maggs PH, Parr JR, Morris MA, de Moerloose P, Neerman-Arbez M.
    Blood; 2003 Dec 15; 102(13):4413-5. PubMed ID: 12893758
    [Abstract] [Full Text] [Related]

  • 3. Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes.
    Neerman-Arbez M, de Moerloose P, Honsberger A, Parlier G, Arnuti B, Biron C, Borg JY, Eber S, Meili E, Peter-Salonen K, Ripoll L, Vervel C, d'Oiron R, Staeger P, Antonarakis SE, Morris MA.
    Hum Genet; 2001 Mar 15; 108(3):237-40. PubMed ID: 11354637
    [Abstract] [Full Text] [Related]

  • 4. Fibrinogen gene mutations accounting for congenital afibrinogenemia.
    Neerman-Arbez M.
    Ann N Y Acad Sci; 2001 Mar 15; 936():496-508. PubMed ID: 11460507
    [Abstract] [Full Text] [Related]

  • 5. Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia.
    Neerman-Arbez M, de Moerloose P, Bridel C, Honsberger A, Schönbörner A, Rossier C, Peerlinck K, Claeyssens S, Di Michele D, d'Oiron R, Dreyfus M, Laubriat-Bianchin M, Dieval J, Antonarakis SE, Morris MA.
    Blood; 2000 Jul 01; 96(1):149-52. PubMed ID: 10891444
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defects.
    Monaldini L, Asselta R, Duga S, Peyvandi F, Karimi M, Malcovati M, Tenchini ML.
    Thromb Haemost; 2007 Apr 01; 97(4):546-51. PubMed ID: 17393016
    [Abstract] [Full Text] [Related]

  • 12. A novel nonsense mutation in the FGA gene in a Chinese family with congenital afibrinogenaemia.
    Wu S, Wang Z, Dong N, Bai X, Ruan C.
    Blood Coagul Fibrinolysis; 2005 Apr 01; 16(3):221-6. PubMed ID: 15795544
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells.
    Neerman-Arbez M, Germanos-Haddad M, Tzanidakis K, Vu D, Deutsch S, David A, Morris MA, de Moerloose P.
    Blood; 2004 Dec 01; 104(12):3618-23. PubMed ID: 15284111
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. [Congenital afibrinogenemia associated with a novel nonsense mutation in the FGA gene].
    Wu SY, Wang ZY, Dong NZ, Bai X, Ruan CG.
    Zhonghua Xue Ye Xue Za Zhi; 2005 Mar 01; 26(3):133-6. PubMed ID: 15946522
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene identified in a compound heterozygous afibrinogenemic patient.
    Platé M, Asselta R, Peyvandi F, Tenchini ML, Duga S.
    Biochim Biophys Acta; 2007 Jul 01; 1772(7):781-7. PubMed ID: 17531448
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.