C3 Glomerulopathy and Atypical Hemolytic Uremic Syndrome: Two Important Manifestations of Complement System Dysfunction
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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C3 Glomerulopathy and Atypical Hemolytic Uremic Syndrome: Two Important Manifestations of Complement System Dysfunction ; volume:8 ; number:1 ; year:2018 ; pages:25-34
Case reports in nephrology and dialysis ; 8, Heft 1 (2018), 25-34
- Creator
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Bajwa, Ravneet
DePalma, John A.
Khan, Taimoor
Cheema, Anmol
Kalathil, Sheila A.
Hossain, Mohammad A.
Haroon, Attiya
Madhurima, Anne
Zheng, Min
Nayer, Ali
Asif, Arif
- DOI
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10.1159/000486848
- URN
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urn:nbn:de:101:1-201805241260
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:26 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Bajwa, Ravneet
- DePalma, John A.
- Khan, Taimoor
- Cheema, Anmol
- Kalathil, Sheila A.
- Hossain, Mohammad A.
- Haroon, Attiya
- Madhurima, Anne
- Zheng, Min
- Nayer, Ali
- Asif, Arif
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Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics
Life-Threatening Extrarenal Manifestations in an Infant with Atypical Hemolytic Uremic Syndrome Caused by a Complement 3-Gene Mutation
Life-Threatening Extrarenal Manifestations in an Infant with Atypical Hemolytic Uremic Syndrome Caused by a Complement 3-Gene Mutation
Genetic abnormalities in biopsy-proven, adult-onset hemolytic uremic syndrome and C3 glomerulopathy
The role of complement autoantibodies in hemolytic uremic syndrome and dense deposit disease
Hemolytic uremic syndrome with simultaneous Shiga toxin producing Escherichia coli and complement abnormalities
C3 mesangial proliferative glomerulonephritis initially presenting with atypical hemolytic uremic syndrome: a case report
Transplantation in Atypical Hemolytic Uremic Syndrome
Complement and the atypical hemolytic uremic syndrome in children
Atypical hemolytic uremic syndrome
Serological and genetic complement alterations in infection-induced and complement-mediated hemolytic uremic syndrome
Complement activation in children with Streptococcus pneumoniae associated hemolytic uremic syndrome
Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics
Life-Threatening Extrarenal Manifestations in an Infant with Atypical Hemolytic Uremic Syndrome Caused by a Complement 3-Gene Mutation
Life-Threatening Extrarenal Manifestations in an Infant with Atypical Hemolytic Uremic Syndrome Caused by a Complement 3-Gene Mutation
Genetic abnormalities in biopsy-proven, adult-onset hemolytic uremic syndrome and C3 glomerulopathy
The role of complement autoantibodies in hemolytic uremic syndrome and dense deposit disease
Hemolytic uremic syndrome with simultaneous Shiga toxin producing Escherichia coli and complement abnormalities
C3 mesangial proliferative glomerulonephritis initially presenting with atypical hemolytic uremic syndrome: a case report