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Quoted phrase not found in phrase index: "Atypical hemolytic-uremic syndrome with B factor anomaly"
Page 1
Inherited Kidney Complement Diseases.
Lemaire M, Noone D, Lapeyraque AL, Licht C, Frémeaux-Bacchi V. Lemaire M, et al. Clin J Am Soc Nephrol. 2021 Jun;16(6):942-956. doi: 10.2215/CJN.11830720. Epub 2021 Feb 3. Clin J Am Soc Nephrol. 2021. PMID: 33536243 Free PMC article. Review.
Staggering progress was realized toward a better understanding of the genetic underpinnings and pathophysiology of many forms of atypical hemolytic uremic syndrome (aHUS) and C3-dominant glomerulopathies that are driven by complement system abnormal …
Staggering progress was realized toward a better understanding of the genetic underpinnings and pathophysiology of many forms of atypical …
Atypical hemolytic uremic syndrome and acute tubular necrosis induced by complement factor B gene (CFB) mutation: A case report.
Wu H, Su S, Li L, Zhang L. Wu H, et al. Medicine (Baltimore). 2021 Mar 19;100(11):e25069. doi: 10.1097/MD.0000000000025069. Medicine (Baltimore). 2021. PMID: 33725982 Free PMC article.
RATIONALE: Atypical hemolytic uremic syndrome (aHUS) is an uncommon and serious disease that manifests hemolytic anemia, thrombocytopenia, and acute kidney injury. Genetic complement abnormalities have been shown to be responsible. Compar …
RATIONALE: Atypical hemolytic uremic syndrome (aHUS) is an uncommon and serious disease that manifests hemoly …
Thrombotic microangiopathies: thrombotic thrombocytopenic purpura / hemolytic uremic syndrome.
Polito MG, Kirsztajn GM. Polito MG, et al. J Bras Nefrol. 2010 Jul-Sep;32(3):303-15. J Bras Nefrol. 2010. PMID: 21103695 Free article.
Thrombotic microangiopathies (TMAs) are pathological conditions characterized by generalized microvascular occlusion by platelet thrombi, thrombocytopenia, and microangiopathic hemolytic anemia. Two typical phenotypes of TMAs are hemolytic- uremic syndrome …
Thrombotic microangiopathies (TMAs) are pathological conditions characterized by generalized microvascular occlusion by platelet thrombi, th …
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. Phillips EH, et al. J Thromb Haemost. 2016 Jan;14(1):175-85. doi: 10.1111/jth.13189. Epub 2016 Jan 11. J Thromb Haemost. 2016. PMID: 26559391 Free PMC article.
ESSENTIALS: Molecular diagnostics has improved the differentiation of acute thrombotic microangiopathys (TMAs). Atypical hemolytic uremic syndrome may have features mimicking thrombotic thrombocytopenic purpura. ...Confirmation of thrombotic thrombocyt …
ESSENTIALS: Molecular diagnostics has improved the differentiation of acute thrombotic microangiopathys (TMAs). Atypical hemolytic …