Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 3 |
2014 | 1 |
2024 | 0 |
Search Results
4 results
Results by year
Filters applied: . Clear all
Quoted phrase not found in phrase index: "Atypical hemolytic-uremic syndrome with thrombomodulin anomaly"
Page 1
Atypical hemolytic uremic syndrome.
Orphanet J Rare Dis. 2011 Sep 8;6:60. doi: 10.1186/1750-1172-6-60.
Orphanet J Rare Dis. 2011.
PMID: 21902819
Free PMC article.
Review.
Hemolytic uremic syndrome (HUS) is defined by the triad of mechanical hemolytic anemia, thrombocytopenia and renal impairment. ...Atypical HUS represents 5 -10% of HUS in children, but the majority of HUS in adults. ...
Hemolytic uremic syndrome (HUS) is defined by the triad of mechanical hemolytic anemia, thrombocytopenia and ren …
Atypical hemolytic uremic syndrome, genetic basis, and clinical manifestations.
Kavanagh D, Goodship TH.
Kavanagh D, et al.
Hematology Am Soc Hematol Educ Program. 2011;2011:15-20. doi: 10.1182/asheducation-2011.1.15.
Hematology Am Soc Hematol Educ Program. 2011.
PMID: 22160007
Atypical hemolytic uremic syndrome (aHUS) is now well recognized to be a disease characterized by excessive complement activation in the microvasculature. In both the familial and sporadic forms, inherited and acquired abnormalities affecting co …
Atypical hemolytic uremic syndrome (aHUS) is now well recognized to be a disease characterized by excessive comp …
Item in Clipboard
Analysis of patients with atypical hemolytic uremic syndrome treated at the Mie University Hospital: concentration of C3 p.I1157T mutation.
Matsumoto T, Fan X, Ishikawa E, Ito M, Amano K, Toyoda H, Komada Y, Ohishi K, Katayama N, Yoshida Y, Matsumoto M, Fujimura Y, Ikejiri M, Wada H, Miyata T.
Matsumoto T, et al.
Int J Hematol. 2014 Nov;100(5):437-42. doi: 10.1007/s12185-014-1655-2. Epub 2014 Aug 19.
Int J Hematol. 2014.
PMID: 25135378
Atypical hemolytic uremic syndrome (aHUS) is caused by abnormalities of the complement system and has a significantly poor prognosis. ...
Atypical hemolytic uremic syndrome (aHUS) is caused by abnormalities of the complement system and has a s …
Item in Clipboard
Postoperative thrombotic thrombocytopenic purpura in an infant: case report and literature review.
Schiller O, Ash S, Schonfeld T, Kadmon G, Nahum E, Yacobovich J, Tamary H, Davidovits M.
Schiller O, et al.
J Pediatr Surg. 2011 Apr;46(4):764-766. doi: 10.1016/j.jpedsurg.2011.01.009.
J Pediatr Surg. 2011.
PMID: 21496552
We present a 14-month-old infant in whom clinical and laboratory abnormalities compatible with thrombotic thrombocytopenic purpura were noted several days after resection of a large pelvic tumor. ...ADAMTS13 inhibitors were negative and no mutations were found in factor H, …
We present a 14-month-old infant in whom clinical and laboratory abnormalities compatible with thrombotic thrombocytopenic purpura we …
Item in Clipboard
Cite
Cite