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

Hypersplenism: History and current status

7 Sept 2016

Abstract excerpt

Hypersplenism is a common disorder characterized by an enlarged spleen which causes rapid and premature destruction of blood cells. This review summarizes the history of hypersplenism, discuss its classification and pathogenesis, and examines its diagnosis and treatment options. We performed a comprehensive literature search using PubMed, Web of Knowledge and the China National Knowledge Infrastructure (CNKI)...

Read the complete abstract on PubMed

Topics

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

Share to Myeloproliferative Neoplasms: Diagnosis and Treatment
Share to Pancreatitis Pathology and Treatment

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 27703501
DOI: 10.3892/etm.2016.3683

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hypersplenism: History and current statusPMID 27703501Read ↗

New Facets of Hematolymphoid Eponymic DiseasesSemantic proximity Read ↗

Diagnosis and Treatment of VOD/SOS After Allogeneic Hematopoietic Stem Cell TransplantationSemantic proximity Read ↗

Disorders of red and white blood cells, such as anemia and leukemiaSemantic proximity Read ↗

Amendment to the guideline for diagnosis and investigation of polycythaemia/erythrocytosisSemantic proximity Read ↗

Hemophagocytic Lymphohistiocytosis: Lessons Learned from the Dark Side.Semantic proximity Read ↗

Primary and secondary hemophagocytic lymphohistiocytosis: clinical features, pathogenesis and therapy.Semantic proximity Read ↗

Diagnosis and management of catastrophic antiphospholipid syndrome.Semantic proximity Read ↗

Hemophagocytic syndrome: primary forms and predisposing conditionsSemantic proximity Read ↗

Pathogenesis of the syndrome of hemolysis, elevated liver enzymes, and low platelet count (HELLP): a reviewSemantic proximity Read ↗

[Research Advances on the Pathogenesis and Treatment of Hemolytic Uremic Syndrome --Review].Semantic proximity Read ↗

Auto immune hepatitis.Semantic proximity Read ↗

POEMS Syndrome: an Enigma.Semantic proximity Read ↗

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