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

168 related items for PubMed ID: 34460979

  • 1. Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population.
    Shen MC, Wang JD, Tsai W, Lin CY, Lin JS, Kuo SF, Lin PT, Huang YC, Hung MH.
    Haemophilia; 2021 Nov; 27(6):1022-1027. PubMed ID: 34460979
    [Abstract] [Full Text] [Related]

  • 2. Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations.
    Tavasoli B, Safa M, Dorgalaleh A, Ghasemi JB, Rezaei Makhouri F, Rezvani MR, Ahmadi A, Tabibian S, Jazebi M, Baghaipour MR, Zaker F.
    Int J Lab Hematol; 2020 Oct; 42(5):619-627. PubMed ID: 32639687
    [Abstract] [Full Text] [Related]

  • 3. Genetic and clinical characterization of congenital fibrinogen disorders in Polish patients: Identification of three novel fibrinogen gamma chain mutations.
    Wypasek E, Klukowska A, Zdziarska J, Zawilska K, Treliński J, Iwaniec T, Mital A, Pietrys D, Sydor W, Neerman-Arbez M, Undas A.
    Thromb Res; 2019 Oct; 182():133-140. PubMed ID: 31479941
    [Abstract] [Full Text] [Related]

  • 4. Congenital fibrinogen disorder caused by digenic mutations of the FGA and FGB genes.
    Wang X, Tang N, Shen N, Lu Y, Li D.
    Hematology; 2020 Dec; 25(1):145-148. PubMed ID: 32228225
    [Abstract] [Full Text] [Related]

  • 5. Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders.
    Mohsenian S, Seidizadeh O, Mirakhorli M, Jazebi M, Azarkeivan A.
    Transfus Apher Sci; 2021 Dec; 60(6):103203. PubMed ID: 34275736
    [Abstract] [Full Text] [Related]

  • 6. Congenital afibrinogenemia: Identification and characterization of two novel homozygous fibrinogen Aα and Bβ chain mutations in two Tunisian families.
    Amri Y, Toumi Nel H, Hadj Fredj S, de Moerloose P.
    Thromb Res; 2016 Jul; 143():11-6. PubMed ID: 27164460
    [Abstract] [Full Text] [Related]

  • 7. 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; 108(3):237-40. PubMed ID: 11354637
    [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.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 14. 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]

  • 15. A novel fibrinogen variant in a Chinese pedigree with congenital dysfibrinogenemia caused by FGA P. Arg38Thr mutation: A case report.
    Cai R, Li Y, Wang W, Gao X, Liu M, Diao Y, Tang Y, Feng Q.
    Medicine (Baltimore); 2018 Oct 01; 97(40):e12697. PubMed ID: 30290666
    [Abstract] [Full Text] [Related]

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

  • 17. Congenital hypofibrinogenemia associated with novel homozygous fibrinogen Aα and heterozygous Bβ chain mutations.
    Castaman G, Rimoldi V, Giacomelli SH, Duga S.
    Thromb Res; 2015 Jul 01; 136(1):144-7. PubMed ID: 25981141
    [Abstract] [Full Text] [Related]

  • 18. Clinical phenotype and laboratory characteristics of 93 patients with congenital fibrinogen disorders from unrelated 36 families.
    Tian D, Liang J, Gao H, Xu X, Nie W, Yin M, Lou J, Shen HQ.
    Res Pract Thromb Haemost; 2024 May 01; 8(4):102445. PubMed ID: 38953055
    [Abstract] [Full Text] [Related]

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

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.