Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Clinical characteristics of hemolytic uremic syndrome secondary to cobalamin C disorder in Chinese children.

World journal of pediatrics : WJP - 1 Aug 2015

Li Qi-Liang, Song Wen-Qi, Peng Xiao-Xia, Liu Xiao-Rong, He Le-Jian, Fu Li-Bing

Abstract excerpt

BACKGROUND: The present study was undertaken to investigate the clinical characteristics of hemolytic uremic syndrome (HUS) secondary to cobalamin C disorder (cbl-C disorder). METHODS: We reviewed retrospectively the medical records of 3 children with HUS secondary to cbl-C disorder who had been treated between April 1, 2009 and October 31, 2013. RESULTS: The 3 patients with HUS secondary to cbl-C disorder...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Hemolytic-Uremic Syndrome
Share to Homocysteine

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Oxidoreductases

Share to Rare Diseases

Share to Sampling Studies

Share to Severity of Illness Index

Share to Vitamin B 12

Share to Vitamin B 12 Deficiency

Source

Identifiers

PMID: 26253414
DOI: 10.1007/s12519-015-0032-4

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical characteristics of hemolytic uremic syndrome secondary to cobalamin C disorder in Chinese children.PMID 26253414Read ↗

Atypical hemolytic uremic syndrome induced by CblC subtype of methylmalonic academia: A case report and literature review.Semantic proximity Read ↗

Cobalamin C defect-hemolytic uremic syndrome caused by new mutation in MMACHC.Semantic proximity Read ↗

Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder.Semantic proximity Read ↗

Late-onset Renal involvement presenting with TMA and tubular injury in cobalamin C disease: a report of three cases and review of the literatureSemantic proximity Read ↗

Adult-onset eculizumab-resistant hemolytic uremic syndrome associated with cobalamin C deficiency.Semantic proximity Read ↗

Advances in our understanding of the pathogenesis of hemolytic uremic syndromes.Semantic proximity Read ↗

Guidelines for diagnosis and management of the cobalamin‐related remethylation disorders cblC, cblD, cblE, cblF, cblG, cblJ and MTHFR deficiencySemantic proximity Read ↗

Cobalamin C defect associated with hemolytic-uremic syndrome.Semantic proximity Read ↗

Cobalamin C deficiency presenting with diffuse alveolar hemorrhage and pulmonary microangiopathy.Semantic proximity Read ↗

Late-onset cobalamin C deficiency Chinese sibling patients with neuropsychiatric presentations.Semantic proximity Read ↗

Late-onset thrombocytic microangiopathy caused by cblC disease: association with a factor H mutation.Semantic proximity Read ↗

[Relationship of genotypes with clinical phenotypes and outcomes in children with cobalamin C type combined methylmalonic aciduria and homocystinuria].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.