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Publications by E. Kaminskas
U.S. Food and Drug Administration Approval: Ruxolitinib for the Treatment of Patients With Intermediate and High-Risk Myelofibrosis
Clinical Cancer Research
Cancer Research
Oncology
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Food and Drug Administration Drug Approval Summary: Sunitinib Malate for the Treatment of Gastrointestinal Stromal Tumor and Advanced Renal Cell Carcinoma
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Transparency and Dermatologic Device Approval by the US Food and Drug Administration
JAMA Dermatology
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Definition and Management of Ruxolitinib Treatment Failure in Myelofibrosis
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Inclusion of Training Patients in US Food and Drug Administration Premarket Approval Cardiovascular Device Studies
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Ruxolitinib as an Emerging Treatment in Myelofibrosis
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Safety and Efficacy of Ruxolitinib in Myelofibrosis Patients Without Splenomegaly
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Efficacy of Ruxolitinib for Myelofibrosis
Expert Opinion on Pharmacotherapy
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Effects of Ruxolitinib Treatment on Metabolic and Nutritional Parameters in Patients With Myelofibrosis From COMFORT-I
Clinical Lymphoma, Myeloma and Leukemia
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