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1. A novel germline JAK2 mutation in familial myeloproliferative neoplasms. Issue 1 (January 2014)

2. Acquired von Willebrand syndrome in myeloproliferative neoplasms with extreme thrombocytosis. Issue 4 (28th July 2021)

3. Common germline variation at the TERT locus contributes to familial clustering of myeloproliferative neoplasms. Issue 12 (26th September 2014)

5. Epidemiology and clinical relevance of mutations in postpolycythemia vera and postessential thrombocythemia myelofibrosis: A study on 359 patients of the AGIMM group. Issue 7 (11th May 2016)

6. Haematological malignancies in relatives of patients affected with myeloproliferative neoplasms. Issue 2 (24th March 2022)

7. Impaired virus‐specific T cell responses in patients with myeloproliferative neoplasms treated with ruxolitinib. Issue 4 (22nd July 2020)

8. Integrative analysis of copy number and gene expression data suggests novel pathogenetic mechanisms in primary myelofibrosis. Issue 7 (25th November 2015)

9. Isolated congenital asplenia: An overlooked cause of thrombocytosis. Issue 8 (17th March 2022)

10. Phenotype variability of patients with post polycythemia vera and post essential thrombocythemia myelofibrosis is associated with the time to progression from polycythemia vera and essential thrombocythemia. (June 2018)