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Journal Abstract Search

172 related items for PubMed ID: 37611541

  • 1. Complement Factor I Gene Variant in an Atypical Hemolytic Uremic Syndrome Triggered by Hypereosinophilia Syndrome.
    Banjongjit A, Kittanamongkolchai W, Kanjanabuch T.
    Nephron; 2023; 147(11):701-706. PubMed ID: 37611541
    [Abstract] [Full Text] [Related]

  • 2. 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; 105(5):960-970. PubMed ID: 38408703
    [Abstract] [Full Text] [Related]

  • 3. Overlapping Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy with Mutation in CFI in a Japanese Patient: A Case Report.
    Osawa K, Yamamoto S, Yamano Y, Kita A, Okamoto K, Kato N, Tatematsu Y, Kojima F, Ohya M, Hara S, Murata SI, Inoue N, Maruyama S, Araki SI.
    Intern Med; 2024 Jun 15; 63(12):1777-1782. PubMed ID: 37926536
    [Abstract] [Full Text] [Related]

  • 4. 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 15; 32(6):584-588. PubMed ID: 28455885
    [Abstract] [Full Text] [Related]

  • 5. 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 Dec 15; 13():909503. PubMed ID: 35720299
    [Abstract] [Full Text] [Related]

  • 6. Living Donor Kidney Transplantation in Atypical Hemolytic Uremic Syndrome: A Case Series.
    Duineveld C, Verhave JC, Berger SP, van de Kar NCAJ, Wetzels JFM.
    Am J Kidney Dis; 2017 Dec 15; 70(6):770-777. PubMed ID: 28821363
    [Abstract] [Full Text] [Related]

  • 7. 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 15; 14(2):340-5. PubMed ID: 26613809
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  • 9. Atypical Hemolytic Uremic Syndrome Presenting as Acute Heart Failure-A Rare Presentation: Diagnosis Supported by Skin Biopsy.
    Kichloo A, Chugh SS, Gupta S, Pandav J, Chander P.
    J Investig Med High Impact Case Rep; 2019 Feb 15; 7():2324709619842905. PubMed ID: 31010328
    [Abstract] [Full Text] [Related]

  • 10. A novel missense mutation in complement factor I predisposes patients to atypical hemolytic uremic syndrome: a case report.
    Wei X, Li J, Zhan X, Tu L, Huang H, Wang Y.
    J Med Case Rep; 2022 Mar 04; 16(1):101. PubMed ID: 35241161
    [Abstract] [Full Text] [Related]

  • 11. A single-center experience of post-transplant atypical hemolytic uremic syndrome.
    Abu Jawdeh BG, Khan MA.
    Clin Nephrol; 2023 Aug 04; 100(2):75-81. PubMed ID: 37288831
    [Abstract] [Full Text] [Related]

  • 12. Atypical Hemolytic Uremic Syndrome (aHUS) and Adenosine Deaminase (ADA)-Deficient Severe Combined Immunodeficiency (SCID)-Two Diseases That Exacerbate Each Other: Case Report.
    Bogdał A, Badeński A, Pac M, Wójcicka A, Badeńska M, Didyk A, Trembecka-Dubel E, Dąbrowska-Leonik N, Walaszczyk M, Matysiak N, Morawiec-Knysak A, Szczepański T, Szczepańska M.
    Int J Mol Sci; 2021 Aug 31; 22(17):. PubMed ID: 34502390
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. COVID-19: a trigger for severe thrombotic microangiopathy in a patient with complement gene variant.
    Pinte L, Sorohan BM, Prohászka Z, Gherghiceanu M, Băicuş C.
    Rom J Intern Med; 2022 Jun 01; 60(2):138-142. PubMed ID: 34997957
    [Abstract] [Full Text] [Related]

  • 15. The roles of homocysteinemia and methylmalonic acidemia in kidney injury in atypical hemolytic uremic syndrome caused by cobalamin C deficiency.
    Wood WD, Elmaghrabi A, Gotway G, Wolf MTF.
    Pediatr Nephrol; 2022 Jun 01; 37(6):1415-1418. PubMed ID: 34854955
    [Abstract] [Full Text] [Related]

  • 16. Atypical hemolytic-uremic syndrome.
    Kaartinen K, Martola L, Meri S.
    Duodecim; 2017 Jun 01; 133(6):539-47. PubMed ID: 29243465
    [Abstract] [Full Text] [Related]

  • 17. Hot Spot of Complement Factor I Rare Variant p.Ile357Met in Patients With Hemolytic Uremic Syndrome.
    Schwotzer N, Fakhouri F, Martins PV, Delmas Y, Caillard S, Zuber J, Moranne O, Mesnard L, Frémeaux-Bacchi V, El-Sissy C.
    Am J Kidney Dis; 2024 Aug 01; 84(2):244-249. PubMed ID: 38423159
    [Abstract] [Full Text] [Related]

  • 18. Thrombotic microangiopathy caused by methionine synthase deficiency: diagnosis and treatment pitfalls.
    Vaisbich MH, Braga A, Gabrielle M, Bueno C, Piazzon F, Kok F.
    Pediatr Nephrol; 2017 Jun 01; 32(6):1089-1092. PubMed ID: 28210839
    [Abstract] [Full Text] [Related]

  • 19. An Infant Case of Streptococcus Pneumoniae-Associated Thrombotic Microangiopathy with Heterozygous CFI Mutation and CFHR3-CFHR1 Deletion.
    Matsumoto Y, Ikezumi Y, Kondoh T, Yokoi K, Nakajima Y, Kumagai N, Kato T, Kurahashi H, Ito T.
    Tohoku J Exp Med; 2022 Oct 25; 258(3):183-193. PubMed ID: 36070894
    [Abstract] [Full Text] [Related]

  • 20. Complement functional tests for monitoring eculizumab treatment in patients with atypical hemolytic uremic syndrome.
    Cugno M, Gualtierotti R, Possenti I, Testa S, Tel F, Griffini S, Grovetti E, Tedeschi S, Salardi S, Cresseri D, Messa P, Ardissino G.
    J Thromb Haemost; 2014 Sep 25; 12(9):1440-8. PubMed ID: 24853860
    [Abstract] [Full Text] [Related]

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