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Journal Abstract Search

287 related items for PubMed ID: 26613809

  • 1. Thrombotic microangiopathy without renal involvement: two novel mutations in complement-regulator genes.
    Peyvandi F, Rossio R, Ferrari B, Lotta LA, Pontiggia S, Ghiringhelli Borsa N, Pizzuti M, Donadelli R, Piras R, Cugno M, Noris M.
    J Thromb Haemost; 2016 Feb; 14(2):340-5. PubMed ID: 26613809
    [Abstract] [Full Text] [Related]

  • 2. The role of ADAMTS-13 activity and complement mutational analysis in differentiating acute thrombotic microangiopathies.
    Phillips EH, Westwood JP, Brocklebank V, Wong EK, Tellez JO, Marchbank KJ, McGuckin S, Gale DP, Connolly J, Goodship TH, Kavanagh D, Scully MA.
    J Thromb Haemost; 2016 Jan; 14(1):175-85. PubMed ID: 26559391
    [Abstract] [Full Text] [Related]

  • 3. The role of von Willebrand factor in thrombotic microangiopathy.
    Noone DG, Riedl M, Licht C.
    Pediatr Nephrol; 2018 Aug; 33(8):1297-1307. PubMed ID: 28748411
    [Abstract] [Full Text] [Related]

  • 4. Complement activation in diseases presenting with thrombotic microangiopathy.
    Meri S.
    Eur J Intern Med; 2013 Sep; 24(6):496-502. PubMed ID: 23743117
    [Abstract] [Full Text] [Related]

  • 5. Thrombotic microangiopathies: thrombotic thrombocytopenic purpura / hemolytic uremic syndrome.
    Polito MG, Kirsztajn GM.
    J Bras Nefrol; 2010 Sep; 32(3):303-15. PubMed ID: 21103695
    [Abstract] [Full Text] [Related]

  • 6. Thrombotic thrombocytopenic purpura.
    Lämmle B, Kremer Hovinga JA, Alberio L.
    J Thromb Haemost; 2005 Aug; 3(8):1663-75. PubMed ID: 16102032
    [Abstract] [Full Text] [Related]

  • 7. Diagnostic approach to microangiopathic hemolytic disorders.
    Kottke-Marchant K.
    Int J Lab Hematol; 2017 May; 39 Suppl 1():69-75. PubMed ID: 28447417
    [Abstract] [Full Text] [Related]

  • 8. Does severe ADAMTS13 deficiency in thrombotic microangiopathy rule out complement-mediated atypical hemolytic uremic syndrome.
    Arumugam V, Bhowmick R, Agarwal I, Arumadi M.
    Saudi J Kidney Dis Transpl; 2019 May; 30(3):701-705. PubMed ID: 31249236
    [Abstract] [Full Text] [Related]

  • 9. A novel CD46 mutation in a patient with microangiopathy clinically resembling thrombotic thrombocytopenic purpura and normal ADAMTS13 activity.
    Rossio R, Lotta LA, Pontiggia S, Borsa NG, Garagiola I, Ardissino G, Mikovic D, Cugno M, Peyvandi F.
    Haematologica; 2015 Mar; 100(3):e87-9. PubMed ID: 25381125
    [No Abstract] [Full Text] [Related]

  • 10. The complex differential diagnosis between thrombotic thrombocytopenic purpura and the atypical hemolytic uremic syndrome: Laboratory weapons and their impact on treatment choice and monitoring.
    Mannucci PM, Cugno M.
    Thromb Res; 2015 Nov; 136(5):851-4. PubMed ID: 26386489
    [Abstract] [Full Text] [Related]

  • 11. Thrombotic thrombocytopenic purpura and other thrombotic microangiopathic hemolytic anemias: diagnosis and classification.
    Shenkman B, Einav Y.
    Autoimmun Rev; 2014 Nov; 13(4-5):584-6. PubMed ID: 24418304
    [Abstract] [Full Text] [Related]

  • 12. Consensus on the standardization of terminology in thrombotic thrombocytopenic purpura and related thrombotic microangiopathies.
    Scully M, Cataland S, Coppo P, de la Rubia J, Friedman KD, Kremer Hovinga J, Lämmle B, Matsumoto M, Pavenski K, Sadler E, Sarode R, Wu H, International Working Group for Thrombotic Thrombocytopenic Purpura.
    J Thromb Haemost; 2017 Feb; 15(2):312-322. PubMed ID: 27868334
    [Abstract] [Full Text] [Related]

  • 13. [Atypical HUS caused by complement-related abnormalities].
    Yoshida Y, Matsumoto M.
    Rinsho Ketsueki; 2015 Feb; 56(2):185-93. PubMed ID: 25765799
    [Abstract] [Full Text] [Related]

  • 14. Von Willebrand factor regulates complement on endothelial cells.
    Noone DG, Riedl M, Pluthero FG, Bowman ML, Liszewski MK, Lu L, Quan Y, Balgobin S, Schneppenheim R, Schneppenheim S, Budde U, James P, Atkinson JP, Palaniyar N, Kahr WH, Licht C.
    Kidney Int; 2016 Jul; 90(1):123-34. PubMed ID: 27236750
    [Abstract] [Full Text] [Related]

  • 15. The D173G mutation in ADAMTS-13 causes a severe form of congenital thrombotic thrombocytopenic purpura. A clinical, biochemical and in silico study.
    Lancellotti S, Peyvandi F, Pagliari MT, Cairo A, Abdel-Azeim S, Chermak E, Lazzareschi I, Mastrangelo S, Cavallo L, Oliva R, De Cristofaro R.
    Thromb Haemost; 2016 Jan; 115(1):51-62. PubMed ID: 26272487
    [Abstract] [Full Text] [Related]

  • 16. Defining the genetics of thrombotic microangiopathies.
    Vieira-Martins P, El Sissy C, Bordereau P, Gruber A, Rosain J, Fremeaux-Bacchi V.
    Transfus Apher Sci; 2016 Apr; 54(2):212-9. PubMed ID: 27177491
    [Abstract] [Full Text] [Related]

  • 17. Modified Ham test for atypical hemolytic uremic syndrome.
    Gavriilaki E, Yuan X, Ye Z, Ambinder AJ, Shanbhag SP, Streiff MB, Kickler TS, Moliterno AR, Sperati CJ, Brodsky RA.
    Blood; 2015 Jun 04; 125(23):3637-46. PubMed ID: 25862562
    [Abstract] [Full Text] [Related]

  • 18. Thrombotic thrombocytopenic purpura: pathogenesis, diagnosis and potential novel therapeutics.
    Saha M, McDaniel JK, Zheng XL.
    J Thromb Haemost; 2017 Oct 04; 15(10):1889-1900. PubMed ID: 28662310
    [Abstract] [Full Text] [Related]

  • 19. An extremely rare splice site mutation in the gene encoding complement factor I in a patient with atypical hemolytic uremic syndrome.
    Ipe TS, Lim J, Reyes MA, Ero M, Leveque C, Lewis B, Kain J.
    J Clin Apher; 2017 Dec 04; 32(6):584-588. PubMed ID: 28455885
    [Abstract] [Full Text] [Related]

  • 20. Genetic variations in complement factors in patients with congenital thrombotic thrombocytopenic purpura with renal insufficiency.
    Fan X, Kremer Hovinga JA, Shirotani-Ikejima H, Eura Y, Hirai H, Honda S, Kokame K, Taleghani MM, von Krogh AS, Yoshida Y, Fujimura Y, Lämmle B, Miyata T.
    Int J Hematol; 2016 Mar 04; 103(3):283-91. PubMed ID: 26830967
    [Abstract] [Full Text] [Related]

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