Serological and genetic complement alterations in infection-induced and complement-mediated hemolytic uremic syndrome
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1432-198X
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
-
Serological and genetic complement alterations in infection-induced and complement-mediated hemolytic uremic syndrome ; day:7 ; month:10 ; year:2016 ; pages:1-13
Pediatric nephrology ; (7.10.2016), 1-13
- Creator
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Westra, Dineke
- Contributor
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Volokhina, Elena B.
Molen, Renate G. van der
Velden, Thea J. A. M. van der
Jeronimus-Klaasen, Annelies
Goertz, Joop
Gracchi, Valentina
Dorresteijn, Eiske M.
Bouts, Antonia H. M.
Keijzer-Veen, Mandy G.
Wijk, Joanna A. E. van
Bakker, Jaap A.
Roos, Anja
Heuvel, Lambert P. van den
Kar, Nicole C. A. J. van de
SpringerLink (Online service)
- DOI
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10.1007/s00467-016-3496-0
- URN
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urn:nbn:de:1111-201611083824
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:47 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Westra, Dineke
- Volokhina, Elena B.
- Molen, Renate G. van der
- Velden, Thea J. A. M. van der
- Jeronimus-Klaasen, Annelies
- Goertz, Joop
- Gracchi, Valentina
- Dorresteijn, Eiske M.
- Bouts, Antonia H. M.
- Keijzer-Veen, Mandy G.
- Wijk, Joanna A. E. van
- Bakker, Jaap A.
- Roos, Anja
- Heuvel, Lambert P. van den
- Kar, Nicole C. A. J. van de
- SpringerLink (Online service)
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Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics
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Hemolytic uremic syndrome with simultaneous Shiga toxin producing Escherichia coli and complement abnormalities
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Life-Threatening Extrarenal Manifestations in an Infant with Atypical Hemolytic Uremic Syndrome Caused by a Complement 3-Gene Mutation
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Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics
The role of complement autoantibodies in hemolytic uremic syndrome and dense deposit disease
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C3 Glomerulopathy and Atypical Hemolytic Uremic Syndrome: Two Important Manifestations of Complement System Dysfunction
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Anti-C5 monoclonal antibody treatment showing pathological resolution of complement-mediated atypical hemolytic uremic syndrome: a case report
A novel missense mutation in complement factor I predisposes patients to atypical hemolytic uremic syndrome: a case report
Complement dysregulation associated with a genetic variant in factor H-related protein 5 in atypical hemolytic uremic syndrome
Life-Threatening Extrarenal Manifestations in an Infant with Atypical Hemolytic Uremic Syndrome Caused by a Complement 3-Gene Mutation