Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients

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Atypical hemolytic uremic syndrome and eculizumab therapy in children.

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Q54207419-C9E8BDB3-0708-4A25-9B19-F77405C30FCC

P2860

Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients

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2017年論文

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Turkish pediatric atypical hem ...... itial analysis of 146 patients

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Turkish pediatric atypical hem ...... itial analysis of 146 patients

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Turkish pediatric atypical hem ...... itial analysis of 146 patients

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Turkish pediatric atypical hem ...... itial analysis of 146 patients

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Turkish pediatric atypical hem ...... itial analysis of 146 patients

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Turkish pediatric atypical hem ...... itial analysis of 146 patients

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Turkish pediatric atypical hem ...... itial analysis of 146 patients

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Bora Gulhan

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Emine Korkmaz

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Mutlu Hayran

http://www.w3.org/2001/XMLSchema#string

Nesrin Besbas

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Oguz Soylemezoglu

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P2860

Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome

Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype

Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome

Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome.

The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20.

Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognition

Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries

Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease.

Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome.

Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome.

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scholarly article

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10.1186/S12882-016-0420-6

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P478

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Fatih Ozaltin

Zeynep Birsin Özçakar

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2017-01-05T00:00:00Z

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28056875

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5217238

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Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients

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P2860

P2860

Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932