Rare Diseases
Records 1 - 4 (of 4 Records) |
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Mast Cell Leukemia: Clinical and Molecular Features and Survival Outcomes of Patients in the ECNM Registry. Kennedy Vanessa E et al. Blood advances 2022 |
Hereditary alpha tryptasemia is a valid genetic biomarker for severe mediator-related symptoms in mastocytosis. Greiner Georg et al. Blood 2020 Aug |
Clinical Significance of DNA Variants in Chronic Myeloid Neoplasms (CMNs): A Report of the Association for Molecular Pathology. McClure Rebecca F et al. The Journal of molecular diagnostics : JMD 2018 Aug |
A precision therapy against cancers driven by KIT/PDGFRA mutations. Evans Erica K et al. Science translational medicine 2017 Nov 9(414) |