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Journal Abstract Search

113 related items for PubMed ID: 12945885

  • 1. A K19E missense mutation in the plasminogen gene is a common cause of familial hypoplasminogenaemia.
    Tefs K, Tait CR, Walker ID, Pietzsch N, Ziegler M, Schuster V.
    Blood Coagul Fibrinolysis; 2003 Jun; 14(4):411-6. PubMed ID: 12945885
    [Abstract] [Full Text] [Related]

  • 2. Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitis.
    Schuster V, Zeitler P, Seregard S, Ozcelik U, Anadol D, Luchtman-Jones L, Meire F, Mingers AM, Schambeck C, Kreth HW.
    Thromb Haemost; 2001 Jun; 85(6):1004-10. PubMed ID: 11434676
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  • 3. Molecular characterization of an Italian patient with plasminogen deficiency and ligneous conjunctivitis.
    Siboni SM, Spreafico M, Menegatti M, Martinelli I, Peyvandi F.
    Blood Coagul Fibrinolysis; 2007 Jan; 18(1):81-4. PubMed ID: 17179833
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  • 4. Functional Fibrinolysis Assays Reveal Different Mechanisms underlying Plasminogen Dysfunction in Ligneous Conjunctivitis.
    Bourrienne MC, Loyau S, Faille D, de Raucourt E, de Mazancourt P, Ho-Tin-Noé B, Gabison E, Ajzenberg N.
    Thromb Haemost; 2020 May; 120(5):758-767. PubMed ID: 32369847
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  • 5. Isolated familial plasminogen deficiency may not be a risk factor for thrombosis.
    Tait RC, Walker ID, Conkie JA, Islam SI, McCall F.
    Thromb Haemost; 1996 Dec; 76(6):1004-8. PubMed ID: 8972025
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  • 6. Compound-heterozygous mutations in the plasminogen gene predispose to the development of ligneous conjunctivitis.
    Schuster V, Seidenspinner S, Zeitler P, Escher C, Pleyer U, Bernauer W, Stiehm ER, Isenberg S, Seregard S, Olsson T, Mingers AM, Schambeck C, Kreth HW.
    Blood; 1999 May 15; 93(10):3457-66. PubMed ID: 10233898
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  • 7. Identification of three novel plasminogen (PLG) gene mutations in a series of 23 patients with low PLG activity.
    Klammt J, Kobelt L, Aktas D, Durak I, Gokbuget A, Hughes Q, Irkec M, Kurtulus I, Lapi E, Mechoulam H, Mendoza-Londono R, Palumbo JS, Steitzer H, Tabbara KF, Ozbek Z, Pucci N, Sotomayor T, Sturm M, Drogies T, Ziegler M, Schuster V.
    Thromb Haemost; 2011 Mar 15; 105(3):454-60. PubMed ID: 21174000
    [Abstract] [Full Text] [Related]

  • 8. Homozygous mutations in the plasminogen gene of two unrelated girls with ligneous conjunctivitis.
    Schuster V, Mingers AM, Seidenspinner S, Nüssgens Z, Pukrop T, Kreth HW.
    Blood; 1997 Aug 01; 90(3):958-66. PubMed ID: 9242524
    [Abstract] [Full Text] [Related]

  • 9. Combined Ala601-Thr-type dysplasminogenaemia and antiphospholipid antibody syndrome in a patient with recurrent thrombosis.
    Iguchi S, Kazama JJ, Ito S, Shimada H, Nishi S, Gejyo F, Higuchi W, Fuse I.
    Thromb Res; 2002 Mar 15; 105(6):513-7. PubMed ID: 12091052
    [Abstract] [Full Text] [Related]

  • 10. Plasminogen deficiency.
    Mehta R, Shapiro AD.
    Haemophilia; 2008 Nov 15; 14(6):1261-8. PubMed ID: 19141167
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  • 13. Novel homozygous mutation of plasminogen in ligneous conjunctivitis: a case report and literature review.
    Xu L, Sun Y, Yang K, Zhao D, Wang Y, Ren S.
    Ophthalmic Genet; 2021 Apr 15; 42(2):105-109. PubMed ID: 33427557
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  • 14. Plasminogen Kanagawa-I, a novel missense mutation, is caused by the amino acid substitution G732R.
    Higuchi Y, Furihata K, Ueno I, Ishikawa S, Okumura N, Tozuka M, Sakurai N.
    Br J Haematol; 1998 Dec 15; 103(3):867-70. PubMed ID: 9858247
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  • 16. Molecular pathogenesis of plasminogen Hakodate: the second Japanese family case of severe type I plasminogen deficiency manifested late-onset multi-organic chronic pseudomembranous mucositis.
    Osaki T, Souri M, Song YS, Izumi N, Law R, Ichinose A.
    J Thromb Thrombolysis; 2016 Aug 15; 42(2):218-24. PubMed ID: 27193180
    [Abstract] [Full Text] [Related]

  • 17. Tranexamic acid-induced ligneous conjunctivitis with renal failure showed reversible hypoplasminogenaemia.
    Song Y, Izumi N, Potts LB, Yoshida A.
    BMJ Case Rep; 2014 May 19; 2014():. PubMed ID: 24842363
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  • 19. [Recurrent arterial thromboembolism in hereditary hypoplasminogenaemia].
    Hagendorff A, Hertfelder HJ, Fehske W, Kirchhoff PG, Malfertheiner P.
    Dtsch Med Wochenschr; 1996 Mar 01; 121(9):263-8. PubMed ID: 8681773
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