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Hereditary myeloproliferative disorders

Name: Hereditary myeloproliferative disorders
Creator: Radek C. Skoda
Keywords: 0301 basic medicine, 03 medical and health sciences, Myeloproliferative Disorders, 0302 clinical medicine, Mutation, Receptors, Erythropoietin, Humans, Diseases of the blood and blood-forming organs, RC633-647.5, 3. Good health

descriptionPublicationkeyboard_double_arrow_right Article , Other literature type 01 Jan 2010 English Publisher:Ferrata Storti Foundation (Haematologica)Journal:Haematologica, volume 95, pages 6-8 (issn: 0390-6078, eissn: 1592-8721,

Authors: Radek C. Skoda;

doi: 10.3324/haematol.2009.015941

pmid: 20065077

pmc: PMC2805753

Hereditary myeloproliferative disorders

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Abstract

Hereditary forms of myeloproliferative disorders (MPD) can be divided into two broad categories. First, inherited syndromes that affect a single lineage with Mendelian inheritance, high penetrance and polyclonal hematopoiesis, and second, inherited predisposition to true MPD, characterized by low

Related Organizations

University Hospital of Basel
Switzerland

Keywords

Myeloproliferative Disorders, Mutation, Receptors, Erythropoietin, Humans, Diseases of the blood and blood-forming organs, RC633-647.5

Impact byBIP!

	citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	21
	popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.	Average
	influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	Top 10%
	impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.	Top 10%