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Journal Abstract Search

290 related items for PubMed ID: 36306276

  • 1. Novel Complement Factor B Gene Mutation Identified in a Kidney Transplant Recipient with a Shiga Toxin-Triggered Episode of Thrombotic Microangiopathy.
    Korzycka J, Pawłowicz-Szlarska E, Masajtis-Zagajewska A, Nowicki M.
    Am J Case Rep; 2022 Oct 28; 23():e936565. PubMed ID: 36306276
    [Abstract] [Full Text] [Related]

  • 2. [Complement factor B mutation in atypical hemolytic uremic syndrome. Rare cause of rare disease].
    Visconti L, Cernaro V, Ardissino G, Sgarbanti M, Ferrara D, Visconti G, Santoro D, Buemi M.
    G Ital Nefrol; 2017 Apr 28; 34(2):74-81. PubMed ID: 28682564
    [Abstract] [Full Text] [Related]

  • 3. Genetics of atypical hemolytic uremic syndrome (aHUS).
    Rodríguez de Córdoba S, Hidalgo MS, Pinto S, Tortajada A.
    Semin Thromb Hemost; 2014 Jun 28; 40(4):422-30. PubMed ID: 24799305
    [Abstract] [Full Text] [Related]

  • 4.
    Bhandari J, Rout P, Sedhai YR.
    ; 2024 01 28. PubMed ID: 32310498
    [Abstract] [Full Text] [Related]

  • 5. Isolated thrombotic microangiopathy of the small intestine in a patient with atypical hemolytic uremic syndrome - a case report.
    Nunius C, Büttner-Herold M, Bertz S, Schiffer M, Buchholz B.
    BMC Nephrol; 2020 Mar 24; 21(1):104. PubMed ID: 32204691
    [Abstract] [Full Text] [Related]

  • 6. 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 24; 14(1):175-85. PubMed ID: 26559391
    [Abstract] [Full Text] [Related]

  • 7. CFH and CFB mutations in Shiga toxin-associated haemolytic uraemic syndrome in a 6-year-old boy.
    Çelakil ME, Yücel BB, Bek K.
    Paediatr Int Child Health; 2020 May 24; 40(2):129-131. PubMed ID: 31242818
    [Abstract] [Full Text] [Related]

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  • 9. Case report: Novel FHR2 variants in atypical Hemolytic Uremic Syndrome: A case study of a translational medicine approach in renal transplantation.
    Stea ED, Skerka C, Accetturo M, Pesce F, Wiech T, Hartman A, Pontrelli P, Conserva F, Castellano G, Zipfel PF, Gesualdo L.
    Front Immunol; 2022 May 24; 13():1008294. PubMed ID: 36451836
    [Abstract] [Full Text] [Related]

  • 10. Post-Transplant Thrombotic Microangiopathy due to a Pathogenic Mutation in Complement Factor I in a Patient With Membranous Nephropathy: Case Report and Review of Literature.
    Saleem M, Shaikh S, Hu Z, Pozzi N, Java A.
    Front Immunol; 2022 May 24; 13():909503. PubMed ID: 35720299
    [Abstract] [Full Text] [Related]

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

  • 12. Diabetic ketoacidosis presenting with atypical hemolytic uremic syndrome associated with a variant of complement factor B in an adult: a case report.
    Zhu Z, Chen H, Gill R, Wang J, Spitalewitz S, Gotlieb V.
    J Med Case Rep; 2016 Feb 24; 10():38. PubMed ID: 26911616
    [Abstract] [Full Text] [Related]

  • 13. Atypical hemolytic uremic syndrome.
    Loirat C, Frémeaux-Bacchi V.
    Orphanet J Rare Dis; 2011 Sep 08; 6():60. PubMed ID: 21902819
    [Abstract] [Full Text] [Related]

  • 14. Atypical hemolytic uremic syndrome: Laboratory characteristics, complement-amplifying conditions, renal biopsy, and genetic mutations.
    Hossain MA, Cheema A, Kalathil S, Bajwa R, Costanzo EJ, Cosentino J, Cheng J, Vachharajani T, Asif A.
    Saudi J Kidney Dis Transpl; 2018 Sep 08; 29(2):276-283. PubMed ID: 29657193
    [Abstract] [Full Text] [Related]

  • 15. [Atypical hemolytic-uremic syndrome related to abnormalities within the complement system].
    Frémeaux-Bacchi V, Fakhouri F, Roumenina L, Dragon-Durey MA, Loirat C.
    Rev Med Interne; 2011 Apr 08; 32(4):232-40. PubMed ID: 21376430
    [Abstract] [Full Text] [Related]

  • 16. [Atypical HUS caused by complement-related abnormalities].
    Yoshida Y, Matsumoto M.
    Rinsho Ketsueki; 2015 Feb 08; 56(2):185-93. PubMed ID: 25765799
    [Abstract] [Full Text] [Related]

  • 17. Complement Gene Variants and Shiga Toxin-Producing Escherichia coli-Associated Hemolytic Uremic Syndrome: Retrospective Genetic and Clinical Study.
    Frémeaux-Bacchi V, Sellier-Leclerc AL, Vieira-Martins P, Limou S, Kwon T, Lahoche A, Novo R, Llanas B, Nobili F, Roussey G, Cailliez M, Ulinski T, Deschênes G, Alberti C, Weill FX, Mariani P, Loirat C.
    Clin J Am Soc Nephrol; 2019 Mar 07; 14(3):364-377. PubMed ID: 30674459
    [Abstract] [Full Text] [Related]

  • 18. Thrombotic microangiopathy after kidney transplantation.
    Noris M, Remuzzi G.
    Am J Transplant; 2010 Jul 07; 10(7):1517-23. PubMed ID: 20642678
    [Abstract] [Full Text] [Related]

  • 19. A case-based narrative review of pregnancy-associated atypical hemolytic uremic syndrome/complement-mediated thrombotic microangiopathy.
    Che M, Moran SM, Smith RJ, Ren KYM, Smith GN, Shamseddin MK, Avila-Casado C, Garland JS.
    Kidney Int; 2024 May 07; 105(5):960-970. PubMed ID: 38408703
    [Abstract] [Full Text] [Related]

  • 20. Where are we with haemolytic uremic syndrome?
    Cavero T, Alonso M.
    Med Clin (Barc); 2018 Oct 23; 151(8):329-335. PubMed ID: 29699703
    [Abstract] [Full Text] [Related]

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