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Article

Essential thrombocythemia A retrospective case series.

Pediatric blood & cancer - 1 May 2020

Barg Assaf Arie, Toren Amos, Tamary Hannah, Yacobovich Joanne, Steinberg-Shemer Orna, Gilad Oded, Goldstein Gal, Miskin Hagit, Revel-Vilk Shoshana, Rosenbeg Nurit, Kenet Gili, Zemer Vered Shkalim

Abstract excerpt

BACKGROUND: Essential thrombocythemia (ET) is rare in children, and pediatric guidelines are lacking. Therefore, we aimed to evaluate ET diagnosis and treatment in a pediatric cohort. PROCEDURE: Data of patients with ET from three hospitals were reviewed. Molecular diagnosis included JAK2V617F, CALR, and MPL mutations. Patients were evaluated for acquired von Willebrand syndrome (AVWS). Follow-up included...

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PMID: 32124556
DOI: 10.1002/pbc.28183

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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.

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