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Publications by T Jimma
SF3B1 Mutations in Primary Myelofibrosis: Clinical, Histopathology and Genetic Correlates Among 155 Patients
Leukemia
Cancer Research
Oncology
Anesthesiology
Pain Medicine
Hematology
Related publications
Frequency and Clinical Correlates of JAK2 46/1 (GGCC) Haplotype in Primary Myelofibrosis
Leukemia
Cancer Research
Oncology
Anesthesiology
Pain Medicine
Hematology
Driver Mutation‐Specific Clinical and Genomic Correlates Differ Between Primary and Secondary Myelofibrosis
American Journal of Hematology
Hematology
Genetic Characterization of SF3B1 Mutations in Single Chronic Lymphocytic Leukemia Cells
Leukemia
Cancer Research
Oncology
Anesthesiology
Pain Medicine
Hematology
Driver Mutations and Prognosis in Primary Myelofibrosis: Mayo-Careggi MPN Alliance Study of 1,095 Patients
American Journal of Hematology
Hematology
Fibrogenesis in Primary Myelofibrosis: Diagnostic, Clinical, and Therapeutic Implications
Oncologist
Cancer Research
Medicine
Oncology
Current Genetic Models for Prediction of Primary Myelofibrosis
Klinicheskaya Onkogematologiya/Clinical Oncohematology
Oncology
Hematology
New Сytogenetic Approaches in Patients With Primary Myelofibrosis
Klinicheskaya Onkogematologiya/Clinical Oncohematology
Oncology
Hematology
Genetic and Clinical Aspects of Zellweger Spectrum Patients With PEX1 Mutations
Journal of Medical Genetics
Genetics
SRSF2 Mutations in Primary Myelofibrosis: Significant Clustering With IDH Mutations and Independent Association With Inferior Overall and Leukemia-Free Survival
Blood
Biochemistry
Immunology
Cell Biology
Hematology
