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

Isolated thrombotic microangiopathy of the small intestine in a patient with atypical hemolytic uremic syndrome - a case report.

BMC nephrology - 24 Mar 2020

Nunius Christoph, Büttner-Herold Maike, Bertz Simone, Schiffer Mario, Buchholz Bjoern

Abstract excerpt

BACKGROUND: Atypical hemolytic uremic syndrome (aHUS) is a rare disease characterized by systemic thrombotic microangiopathy (TMA) reflected by hemolysis, anemia, thrombocytopenia and systemic organ injury. The optimal management of aHUS-patients when undergoing kidney transplantation to prevent recurrence in the allograft is eculizumab, an approved recombinant antibody targeting human complement component C5....

Read the complete abstract on PubMed

Topics

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

Share to Antibodies, Monoclonal, Humanized
Share to Atypical Hemolytic Uremic Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Endoscopy, Gastrointestinal

Share to Graft Rejection

Share to Intestine, Small

Share to Kidney Failure, Chronic

Share to Membrane Cofactor Protein

Share to Renal Dialysis

Source

Open in PubMed Open full text

Identifiers

PMID: 32204691
DOI: 10.1186/s12882-020-01766-0
PMCID: PMC7092568

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Isolated thrombotic microangiopathy of the small intestine in a patient with atypical hemolytic uremic syndrome - a case report.PMID 32204691Read ↗

[Atypical hemolytic uremic syndrome].Semantic proximity Read ↗

Consensus regarding diagnosis and management of atypical hemolytic uremic syndromeSemantic proximity Read ↗

An update for atypical haemolytic uraemic syndrome: Diagnosis and treatment. A consensus documentSemantic proximity Read ↗

Spectrum of Complement-Mediated Thrombotic Microangiopathies: Pathogenetic Insights Identifying Novel Treatment ApproachesSemantic proximity Read ↗

A single-center experience of post-transplant atypical hemolytic uremic syndrome.Semantic proximity Read ↗

Atypical hemolytic uremic syndrome: Laboratory characteristics, complement-amplifying conditions, renal biopsy, and genetic mutations.Semantic proximity Read ↗

Thrombotic microangiopathy: focus on atypical hemolytic uremic syndrome.Semantic proximity Read ↗

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

Pathogenesis and prognosis of thrombotic microangiopathy.Semantic proximity Read ↗

Impact of hypertensive emergency and rare complement variants on the presentation and outcome of atypical hemolytic uremic syndromeSemantic proximity Read ↗

Atypical Hemolytic Uremic Syndrome: A Meta-Analysis of Case Reports Confirms the Prevalence of Genetic Mutations and the Shift of Treatment Regimens.Semantic proximity Read ↗

Small vessels, big trouble in the kidneys and beyond: hematopoietic stem cell transplantation–associated thrombotic microangiopathySemantic proximity Read ↗

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