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

96 related items for PubMed ID: 12193975

  • 1. [Molecular variants of fibrinogen].
    Plendl H, Caliebe A, Grote W.
    Hamostaseologie; 2002 May; 22(2):36-41. PubMed ID: 12193975
    [Abstract] [Full Text] [Related]

  • 2. Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain.
    Benson MD, Liepnieks J, Uemichi T, Wheeler G, Correa R.
    Nat Genet; 1993 Mar; 3(3):252-5. PubMed ID: 8097946
    [Abstract] [Full Text] [Related]

  • 3. Hereditary renal amyloidosis with a novel variant fibrinogen.
    Uemichi T, Liepnieks JJ, Benson MD.
    J Clin Invest; 1994 Feb; 93(2):731-6. PubMed ID: 8113408
    [Abstract] [Full Text] [Related]

  • 4. Fibrinogen Baltimore IV: congenital dysfibrinogenemia with delayed fibrin monomer polymerization.
    Ebert RF, Bell WR.
    Thromb Res; 1985 Apr 15; 38(2):121-8. PubMed ID: 4002201
    [Abstract] [Full Text] [Related]

  • 5. Molecular characterization of 7 patients affected by dys- or hypo-dysfibrinogenemia: Identification of a novel mutation in the fibrinogen Bbeta chain causing a gain of glycosylation.
    Asselta R, Robusto M, Platé M, Santoro C, Peyvandi F, Duga S.
    Thromb Res; 2015 Jul 15; 136(1):168-74. PubMed ID: 26006300
    [Abstract] [Full Text] [Related]

  • 6. "Fibrinogen Tokyo II". An abnormal fibrinogen with an impaired polymerization site on the aligned DD domain of fibrin molecules.
    Matsuda M, Baba M, Morimoto K, Nakamikawa C.
    J Clin Invest; 1983 Sep 15; 72(3):1034-41. PubMed ID: 6886002
    [Abstract] [Full Text] [Related]

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

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

  • 9. [Congenital dysfibrinogenemia. Apropos of 13 cases].
    Corrihons G, Soria J, Soria C, Conard J, Horellou MH, Samama M.
    Sem Hop; 1983 Oct 13; 59(36):2517-23. PubMed ID: 6316508
    [Abstract] [Full Text] [Related]

  • 10. Unrecognized Fibrinogen A α-Chain Amyloidosis: Results From Targeted Genetic Testing.
    Tavares I, Oliveira JP, Pinho A, Moreira L, Rocha L, Santos J, Pinheiro J, Costa PP, Lobato L.
    Am J Kidney Dis; 2017 Aug 13; 70(2):235-243. PubMed ID: 28359658
    [Abstract] [Full Text] [Related]

  • 11. [Fibrinolysis in dysfibrinogenemia].
    Witt I.
    Hamostaseologie; 2002 May 13; 22(2):11-2. PubMed ID: 12193971
    [No Abstract] [Full Text] [Related]

  • 12. Rare inherited disorders of fibrinogen.
    Acharya SS, Dimichele DM.
    Haemophilia; 2008 Nov 13; 14(6):1151-8. PubMed ID: 19141154
    [Abstract] [Full Text] [Related]

  • 13. Fibrinogen Bergamo III and fibrinogen Torino: two further variants with hereditary molecular defects in fibrinopeptide A.
    Reber P, Furlan M, Beck EA, Barbui T.
    Thromb Res; 1987 Apr 01; 46(1):163-7. PubMed ID: 3590111
    [No Abstract] [Full Text] [Related]

  • 14. [Aortocoronary venous bypass in dysfibrinogenemia].
    Neidhardt B, Schricker KT, Weniger J.
    Med Welt; 1983 Jan 28; 34(4):119-22. PubMed ID: 6600811
    [No Abstract] [Full Text] [Related]

  • 15. Successful living-related kidney transplantation in a boy with inherited dysfibrinogenemia.
    Imamura H, Akioka Y, Asano T, Sugawara N, Ishizuka K, Chikamoto H, Taki M, Terasawa F, Okumura N, Hattori M.
    Pediatr Transplant; 2013 Nov 28; 17(7):E161-4. PubMed ID: 23962069
    [Abstract] [Full Text] [Related]

  • 16. [Blood coagulation disorders caused by genetic variants of fibrinogen].
    Fiedler H.
    Z Arztl Fortbild (Jena); 1970 Sep 15; 64(18):913-8. PubMed ID: 4922245
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. [Familial dysfibrinogenemia with abnormal nonomer aggregation. Paris III fibrinogen].
    Soria J, Soria C.
    Pathol Biol (Paris); 1974 Nov 15; 22 suppl():72-9. PubMed ID: 4620099
    [No Abstract] [Full Text] [Related]

  • 19. Three abnormal fibrinogen variants with the same amino acid substitution (gamma 275 Arg----His): fibrinogens Bergamo II, Essen and Perugia.
    Reber P, Furlan M, Henschen A, Kaudewitz H, Barbui T, Hilgard P, Nenci GG, Berrettini M, Beck EA.
    Thromb Haemost; 1986 Dec 15; 56(3):401-6. PubMed ID: 3563970
    [Abstract] [Full Text] [Related]

  • 20. Two novel mutations in the fibrinogen γ nodule.
    Kotlín R, Pastva O, Stikarová J, Hlaváčková A, Suttnar J, Chrastinová L, Riedel T, Salaj P, Dyr JE.
    Thromb Res; 2014 Oct 15; 134(4):901-8. PubMed ID: 25074738
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.