Literature DB >> 24523226

CALR mutations are rare in childhood essential thrombocythemia.

Stephen E Langabeer1, Karl Haslam, Corrina McMahon.   

Abstract

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Year:  2014        PMID： 24523226     DOI： 10.1002/pbc.24984

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN： 1545-5009            Impact factor:   3.167


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  4 in total

1.  Mutational profile of childhood myeloproliferative neoplasms.

Authors:  A Karow; R Nienhold; P Lundberg; E Peroni; M C Putti; M L Randi; R C Skoda
Journal:  Leukemia       Date:  2015-07-30       Impact factor: 11.528

2.  Genetic analysis of five children with essential thrombocytosis identified mutations in cancer-associated genes with roles in transcriptional regulation.

Authors:  Nicole Kucine; Aaron D Viny; Raajit Rampal; Michael Berger; Nicholas Socci; Agnes Viale; James B Bussel; Ross L Levine; Franck Rapaport
Journal:  Haematologica       Date:  2016-03-18       Impact factor: 9.941

3.  Distinct molecular abnormalities underlie unique clinical features of essential thrombocythemia in children.

Authors:  R Fu; D Liu; Z Cao; S Zhu; H Li; H Su; L Zhang; F Xue; X Liu; X Zhang; T Cheng; R Yang; L Zhang
Journal:  Leukemia       Date:  2015-06-29       Impact factor: 11.528

4.  Characteristics and outcomes of patients with essential thrombocythemia or polycythemia vera diagnosed before 20 years of age: a systematic review.

Authors:  Jean-Christophe Ianotto; Natalia Curto-Garcia; Marie Lauermanova; Deepti Radia; Jean-Jacques Kiladjian; Claire N Harrison
Journal:  Haematologica       Date:  2019-01-24       Impact factor: 9.941
  4 in total

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