29 results on '"Finke, Christy"'
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2. Clonal Hematopoiesis of Indeterminate Potential Is Associated With Coronary Microvascular Dysfunction In Early Nonobstructive Coronary Artery Disease
3. Driver mutations and prognosis in primary myelofibrosis: Mayo‐Careggi MPN alliance study of 1,095 patients
4. Therapy related‐chronic myelomonocytic leukemia (CMML): Molecular, cytogenetic, and clinical distinctions from de novo CMML
5. Nucleophosmin 1 (NPM1) mutations in chronic myelomonocytic leukemia and their prognostic relevance
6. Supplement to: A pilot study of the telomerase inhibitor imetelstat for myelofibrosis.
7. DNMT3A mutations are associated with inferior overall and leukemia‐free survival in chronic myelomonocytic leukemia
8. Calreticulin variant stratified driver mutational status and prognosis in essential thrombocythemia
9. Predictors of survival in refractory anemia with ring sideroblasts and thrombocytosis (RARS-T) and the role of next-generation sequencing
10. Concurrent activating KIT mutations in systemic mastocytosis
11. Targeted next generation sequencing of PDGFRB rearranged myeloid neoplasms with monocytosis
12. A Pilot Study of the Telomerase Inhibitor Imetelstat for Myelofibrosis
13. ASXL1 mutations are frequent and prognostically detrimental in CSF3R-mutated chronic neutrophilic leukemia
14. A compendium of cytogenetic abnormalities in myelofibrosis: molecular and phenotypic correlates in 826 patients
15. Mutations and thrombosis in essential thrombocythemia: prognostic interaction with age and thrombosis history
16. Molecular and prognostic correlates of cytogenetic abnormalities in chronic myelomonocytic leukemia: a Mayo Clinic-French Consortium Study
17. Type 1 versus Type 2 calreticulin mutations in essential thrombocythemia: A collaborative study of 1027 patients
18. Associations and prognostic interactions between circulating levels of hepcidin, ferritin and inflammatory cytokines in primary myelofibrosis
19. Spliceosome mutations involving SRSF2, SF3B1, and U2AF35 in chronic myelomonocytic leukemia: Prevalence, clinical correlates, and prognostic relevance
20. Plasma cytokines in polycythemia vera: Phenotypic correlates, prognostic relevance, and comparison with myelofibrosis
21. TP53 mutations and polymorphisms in primary myelofibrosis
22. Pruritus in primary myelofibrosis: Clinical and laboratory correlates
23. One Thousand Patients With Primary Myelofibrosis: The Mayo Clinic Experience
24. Vitamin D insufficiency in myeloproliferative neoplasms and myelodysplastic syndromes: Clinical correlates and prognostic studies
25. Infrequent occurrence of MPL exon 10 mutations in polycythemia vera and post-polycythemia vera myelofibrosis
26. Isolated del(5q) in myeloid malignancies: Clinicopathologic and molecular features in 143 consecutive patients
27. Circulating levels of MCP-1, sIL-2R, IL-15, and IL-8 predict anemia response to pomalidomide therapy in myelofibrosis
28. Cytogenetic studies at diagnosis in polycythemia vera: clinical and JAK2V617F allele burden correlates
29. Clinical Correlates of Jak2V617f Allele Burden in Essential Thrombocythemia
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