Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
1996 2
1998 1
2008 1
2009 2
2010 2
2012 1
2013 1
2014 2
2015 1
2016 1
2017 1
2018 3
2019 2
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

19 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Hemolytic uremic syndrome, atypical, childhood"
Page 1
Hemolytic-Uremic Syndrome in childhood.
Vaisbich MH. Vaisbich MH. J Bras Nefrol. 2014 Apr-Jun;36(2):208-20. doi: 10.5935/0101-2800.20140032. J Bras Nefrol. 2014. PMID: 25055362 Free article. Review. English, Portuguese.
Among these we emphasize the thrombotic thrombocytopenic purpura and Hemolytic Uremic Syndrome, and the latter can occur by the action of toxins, systemic diseases, overactivation of the alternative complement system pathway, which can occur due to changes in …
Among these we emphasize the thrombotic thrombocytopenic purpura and Hemolytic Uremic Syndrome, and the latter can occu …
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype.
Noris M, Caprioli J, Bresin E, Mossali C, Pianetti G, Gamba S, Daina E, Fenili C, Castelletti F, Sorosina A, Piras R, Donadelli R, Maranta R, van der Meer I, Conway EM, Zipfel PF, Goodship TH, Remuzzi G. Noris M, et al. Clin J Am Soc Nephrol. 2010 Oct;5(10):1844-59. doi: 10.2215/CJN.02210310. Epub 2010 Jul 1. Clin J Am Soc Nephrol. 2010. PMID: 20595690 Free PMC article.
BACKGROUND AND OBJECTIVES: Hemolytic uremic syndrome (HUS) is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and renal impairment. Most childhood cases are caused by Shiga toxin-producing bacteria. The other form, atypi …
BACKGROUND AND OBJECTIVES: Hemolytic uremic syndrome (HUS) is characterized by microangiopathic hemolytic anemia …
The Role of the Complement System in the Pathogenesis of Infectious Forms of Hemolytic Uremic Syndrome.
Avdonin PP, Blinova MS, Generalova GA, Emirova KM, Avdonin PV. Avdonin PP, et al. Biomolecules. 2023 Dec 27;14(1):39. doi: 10.3390/biom14010039. Biomolecules. 2023. PMID: 38254639 Free PMC article. Review.
Hemolytic uremic syndrome (HUS) is an acute disease and the most common cause of childhood acute renal failure. ...They account for up to 90% of all cases of HUS. The remaining 10% of cases grouped under the general term atypical HUS represent a …
Hemolytic uremic syndrome (HUS) is an acute disease and the most common cause of childhood acute renal failure. …
Extra-Renal manifestations of atypical hemolytic uremic syndrome in children.
Fidan K, Göknar N, Gülhan B, Melek E, Yıldırım ZY, Baskın E, Hayran M, Gülleroglu K, Özçakar ZB, Ozaltin F, Soylemezoglu O. Fidan K, et al. Pediatr Nephrol. 2018 Aug;33(8):1395-1403. doi: 10.1007/s00467-018-3933-3. Epub 2018 Apr 2. Pediatr Nephrol. 2018. PMID: 29610995
BACKGROUND: Atypical hemolytic uremic syndrome (aHUS) is a chronic disease characterized by thrombotic microangiopathy and a high risk of end-stage kidney disease. ...This study aimed to determine the clinical characteristics of patients with extrarena …
BACKGROUND: Atypical hemolytic uremic syndrome (aHUS) is a chronic disease characterized by thrombotic microangi …
Clinical and genetic predictors of atypical hemolytic uremic syndrome phenotype and outcome.
Schaefer F, Ardissino G, Ariceta G, Fakhouri F, Scully M, Isbel N, Lommelé Å, Kupelian V, Gasteyger C, Greenbaum LA, Johnson S, Ogawa M, Licht C, Vande Walle J, Frémeaux-Bacchi V; Global aHUS Registry. Schaefer F, et al. Kidney Int. 2018 Aug;94(2):408-418. doi: 10.1016/j.kint.2018.02.029. Epub 2018 Jun 19. Kidney Int. 2018. PMID: 29907460 Free article.
Atypical hemolytic uremic syndrome (aHUS) is a rare, genetic, life-threatening disease. ...Initial presentation in childhood significantly predicted ESRD risk (adjusted hazard ratio 0.55 [95% confidence interval 0.41-0.73], whereas sex, race, fa …
Atypical hemolytic uremic syndrome (aHUS) is a rare, genetic, life-threatening disease. ...Initial presentation …
Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome.
Ariceta G, Besbas N, Johnson S, Karpman D, Landau D, Licht C, Loirat C, Pecoraro C, Taylor CM, Van de Kar N, Vandewalle J, Zimmerhackl LB; European Paediatric Study Group for HUS. Ariceta G, et al. Pediatr Nephrol. 2009 Apr;24(4):687-96. doi: 10.1007/s00467-008-0964-1. Epub 2008 Sep 18. Pediatr Nephrol. 2009. PMID: 18800230
This guideline for the investigation and initial treatment of atypical hemolytic uremic syndrome (HUS) is intended to offer an approach based on opinion, as evidence is lacking. ...Their management, which is outside the remit of this guideline, is rela …
This guideline for the investigation and initial treatment of atypical hemolytic uremic syndrome (HUS) is intend …
Typical and atypical hemolytic uremic syndrome.
Proesmans W. Proesmans W. Kidney Blood Press Res. 1996;19(3-4):205-8. doi: 10.1159/000174075. Kidney Blood Press Res. 1996. PMID: 8887262 Review.
The hemolytic uremic syndrome is the most frequent cause of acute renal failure in childhood. ...D (+) HUS has also been labeled 'typical HUS' and D (-) HUS as 'atypical HUS'. This has led to some oversimplification, in that atypical has …
The hemolytic uremic syndrome is the most frequent cause of acute renal failure in childhood. ...D (+) HUS has a …
Novel aspects of atypical haemolytic uraemic syndrome and the role of eculizumab.
Verhave JC, Wetzels JF, van de Kar NC. Verhave JC, et al. Nephrol Dial Transplant. 2014 Sep;29 Suppl 4:iv131-41. doi: 10.1093/ndt/gfu235. Nephrol Dial Transplant. 2014. PMID: 25165180 Review.
The haemolytic uraemic syndrome (HUS) is part of a spectrum of thrombotic microangiopathies. The most common etiologies of HUS are the ones seen in childhood caused by an infection of Shiga toxin-producing Escherichia coli, HUS caused by an infection with Streptococ …
The haemolytic uraemic syndrome (HUS) is part of a spectrum of thrombotic microangiopathies. The most common etiologies of HUS are th …
Complement deficiencies and dysregulation: Pathophysiological consequences, modern analysis, and clinical management.
Schröder-Braunstein J, Kirschfink M. Schröder-Braunstein J, et al. Mol Immunol. 2019 Oct;114:299-311. doi: 10.1016/j.molimm.2019.08.002. Epub 2019 Aug 14. Mol Immunol. 2019. PMID: 31421540 Review.
While being rare, diseases related to complement deficiencies are often severe with a frequent but not exclusive manifestation during childhood. Whereas defects of early components of the classical pathway significantly increase the risk of autoimmune disorders, lack of co …
While being rare, diseases related to complement deficiencies are often severe with a frequent but not exclusive manifestation during chi …
Pathophysiology and management of thrombotic microangiopathies.
Ruggenenti P, Remuzzi G. Ruggenenti P, et al. J Nephrol. 1998 Nov-Dec;11(6):300-10. J Nephrol. 1998. PMID: 10048496 Review.
Hemolytic uremic syndrome (HUS) and thrombotic thrombocytopenic purpura (TTP) are syndromes of microangiopathic hemolytic anemia, and thrombocytopenia in which endothelial dysfunction appears to be an important factor in the sequence of events leading …
Hemolytic uremic syndrome (HUS) and thrombotic thrombocytopenic purpura (TTP) are syndromes of microangiopathic hemo …
19 results