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Genome Medicine|May 8, 2015
Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disordersSarah K Westbury, Ernest Turro, Daniel Greene, et al.Allergologie Select|March 11, 2022
S3 guideline Allergy PreventionMatthias V Kopp, Cathleen Muche-Borowski, Michael Abou-Dakn, et al.Science Translational Medicine|March 4, 2016
A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologiesErnest Turro, Daniel Greene, Anouck Wijgaerts, et al.Blood|February 26, 2016
A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing lossSimon Stritt, Paquita Nurden, Ernest Turro, et al.The Journal of Allergy and Clinical Immunology|December 31, 2019
Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) scoreVictoria Katharina Tesch, Hassan Abolhassani, Bella Shadur, et al.Blood|April 17, 2016
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disordersIlenia Simeoni, Jonathan C Stephens, Fengyuan Hu, et al.Physical Review Letters|March 28, 2025
Observation of the Open-Charm Tetraquark Candidate T_{cs0}^{*}(2870)^{0} in the B^{-}→D^{-}D^{0}K_{S}^{0} DecayR Aaij, A S W Abdelmotteleb, C Abellan Beteta, et al.Physical Review Letters|January 30, 2026
Observation of B_{c}^{+}→Dh^{+}h^{-} DecaysR Aaij, A S W Abdelmotteleb, C Abellan Beteta, et al.Physical Review Letters|December 19, 2025
Observation of Orbitally Excited B_{c}^{+} StatesR Aaij, A S W Abdelmotteleb, C Abellan Beteta, et al.Physical Review Letters|June 22, 2026
Measurement of the Top-Quark Production Cross Section and Charge Asymmetry at LHCbR Aaij, A S W Abdelmotteleb, C Abellan Beteta, et al.Pageof 49