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

218 related items for PubMed ID: 28211264

  • 21. The molecular basis of quantitative fibrinogen disorders.
    Asselta R, Duga S, Tenchini ML.
    J Thromb Haemost; 2006 Oct; 4(10):2115-29. PubMed ID: 16999847
    [Abstract] [Full Text] [Related]

  • 22. A novel missense mutation (FGG c.1168G > T) in the gamma chain of fibrinogen causing congenital hypodysfibrinogenemia with bleeding phenotype.
    Xu N, Zheng L, Dai Z, Zhu J, Xie P, Yang S, Chen F.
    Hereditas; 2024 Jan 18; 161(1):4. PubMed ID: 38233949
    [Abstract] [Full Text] [Related]

  • 23. Combined Congenital Hypodysfibrinogemia and Factor XI Deficiency in a Chinese Family.
    Peng Y, Nie L, Qin C, Wan L, Zhou P.
    Acta Haematol; 2020 Jan 18; 143(5):472-477. PubMed ID: 31982874
    [Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. Hypodysfibrinogenaemia due to production of mutant fibrinogen alpha-chains lacking fibrinopeptide A and polymerisation knob 'A'.
    Vorjohann S, Fish RJ, Biron-Andréani C, Nagaswami C, Weisel JW, Boulot P, Reyftmann L, de Moerloose P, Neerman-Arbez M.
    Thromb Haemost; 2010 Nov 18; 104(5):990-7. PubMed ID: 20806111
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. Rare inherited disorders of fibrinogen.
    Acharya SS, Dimichele DM.
    Haemophilia; 2008 Nov 18; 14(6):1151-8. PubMed ID: 19141154
    [Abstract] [Full Text] [Related]

  • 31. Mutations Accounting for Congenital Fibrinogen Disorders: An Update.
    Richard M, Celeny D, Neerman-Arbez M.
    Semin Thromb Hemost; 2022 Nov 18; 48(8):889-903. PubMed ID: 35073585
    [Abstract] [Full Text] [Related]

  • 32. Differences in the function and secretion of congenital aberrant fibrinogenemia between heterozygous γD320G (Okayama II) and γΔN319-ΔD320 (Otsu I).
    Mukai S, Ikeda M, Takezawa Y, Sugano M, Honda T, Okumura N.
    Thromb Res; 2015 Dec 18; 136(6):1318-24. PubMed ID: 26573395
    [Abstract] [Full Text] [Related]

  • 33. Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.
    Mohsenian S, Palla R, Menegatti M, Cairo A, Lecchi A, Casini A, Neerman-Arbez M, Asselta R, Scardo S, Siboni SM, Blatny J, Zapletal O, Schved JF, Giansily-Blaizot M, Halimeh S, Daoud MA, Platokouki H, Pergantou H, Schutgens REG, Van Haaften-Spoor M, Brons P, Laros-van Gorkom B, Van Pinxten E, Borhany M, Fatima N, Mikovic D, Saracevic M, Özdemir GN, Ay Y, Makris M, Lockley C, Mumford A, Harvey A, Austin S, Shapiro A, Williamson A, McGuinn C, Goldberg I, De Moerloose P, Peyvandi F.
    Blood Adv; 2024 Mar 26; 8(6):1392-1404. PubMed ID: 38286442
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No 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. Congenital Hypodysfibrinogenemia due to γ326Cys→Tyr Mutation: Third Ever-Described Case Associated with Recurrent Venous Thrombosis and COVID Vaccine.
    Nanthan KR, Pedersen IS, Andersen DT, Bor MV.
    Acta Haematol; 2024 Mar 26; 147(5):564-570. PubMed ID: 39140696
    [Abstract] [Full Text] [Related]

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

  • 40. Molecular genetics of quantitative fibrinogen disorders.
    Asselta R, Spena S, Duga S, Tenchini ML.
    Cardiovasc Hematol Agents Med Chem; 2007 Apr 26; 5(2):163-73. PubMed ID: 17430139
    [Abstract] [Full Text] [Related]

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