Showing results (321-330 of 420) with videos related to
Sort By:
Pageof 42
Annals of Hematology|June 23, 2022
Gilteritinib monotherapy for relapsed/refractory FLT3 mutated acute myeloid leukemia: a real-world, multi-center, matched analysisShai Shimony, Jonathan Canaani, Eitan Kugler, et al.Neurology|December 20, 2024
Cerebral Hemodynamic Responses to Disease-Modifying and Curative Sickle Cell Disease TherapiesMegan A Aumann, Wesley Richerson, Alexander K Song, et al.Oncogene|November 12, 2013
Increased leukocyte survival and accelerated onset of lymphoma in the absence of MCL-1 S159-phosphorylationS E Lindner, M Wissler, A Gründer, et al.G3 (Bethesda, Md.)|March 29, 2023
Genomic and cytogenetic analysis of the Ceratitis capitata temperature-sensitive lethal regionGermano Sollazzo, Georgia Gouvi, Katerina Nikolouli, et al.Journal of Pediatric Hematology/Oncology|June 6, 2022
Mismatched Unrelated Donor Hematopoietic Stem Cell Transplantation Rescues Marrow Failure From Acute Leukemia Therapy in a Patient With Previously Undiagnosed Ligase IV SyndromeDiana M Fridlyand, Shanmuganathan Chandrakasan, Ahmed Aljudi, et al.Lung Cancer (Amsterdam, Netherlands)|November 1, 1996
Second primary lung cancer in Flanders: frequency, clinical presentation, treatment and prognosisJ Van Meerbeeck, J Weyler, A Thibaut, et al.The Journal of Clinical Endocrinology and Metabolism|August 5, 2004
Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effectGuntram Borck, A Kemal Topaloglu, Eckhard Korsch, et al.Hamostaseologie|September 4, 2012
Desmopressin testing in haemophilia A patients and carriers: results of a multi centre surveyR Knöfler, J Koscielny, J T Tauer, et al.European Journal of Haematology|May 31, 2023
Venetoclax-based salvage therapy for adult patients with relapsed/refractory acute lymphoblastic leukemiaJonathan Canaani, Avraham Frisch, Daniel A Pollyea, et al.Blood|October 24, 2002
von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTPReinhard Schneppenheim, Ulrich Budde, Florian Oyen, et al.Pageof 42