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Article

Atypical haemolytic uraemic syndrome in a Japanese patient with DGKE genetic mutations.

Thrombosis and haemostasis - 1 Oct 2015

Miyata Toshiyuki, Uchida Yumiko, Ohta Toshiyuki, Urayama Kohtaro, Yoshida Yoko, Fujimura Yoshihiro

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Share to Antibodies, Monoclonal, Humanized
Share to Atypical Hemolytic Uremic Syndrome
Share to Databases, Factual
Share to Diacylglycerol Kinase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Mutation, Missense

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Source

Identifiers

PMID: 26018111
DOI: 10.1160/TH15-01-0007

Genes

DGKE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

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Atypical haemolytic uraemic syndrome in a Japanese patient with DGKE genetic mutations.PMID 26018111Read ↗

Atypical hemolytic uremic syndrome due to DGKE mutation and response to eculizumab: lessons for the clinical nephrologist.Semantic proximity Read ↗

Early infantile onset of atypical hemolytic-uremic syndrome is caused by recessive mutations in DGKE.Semantic proximity Read ↗

Various phenotypes of disease associated with mutated DGKE gene.Semantic proximity Read ↗

DGKE and atypical HUS.Semantic proximity Read ↗

A novel compound heterozygous mutation in DGKE in a Chinese patient causes atypical hemolytic uremic syndrome.Semantic proximity Read ↗

Genetics: Hidden intronic mutations in DGKE are causative of aHUS.Semantic proximity Read ↗

A patient with a homozygous diacylglycerol kinase epsilon (DGKE) gene mutation with atypical haemolytic uraemic syndrome and low C3 responded well to eculizumab: a case report.Semantic proximity Read ↗

Phenotypic expansion of DGKE-associated diseases.Semantic proximity Read ↗

Atypical hemolytic uremic syndrome: the role of complement pathway gene mutation analysis.Semantic proximity Read ↗

Atypical haemolytic uraemic syndrome: a case of rare genetic mutation.Semantic proximity Read ↗

Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome.Semantic proximity Read ↗

CD46-associated atypical hemolytic uremic syndrome with uncommon course caused by cblC deficiency.Semantic proximity Read ↗

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