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Frontiers in Genetics|September 7, 2023
Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHDClaudia Strafella, Valerio Caputo, Sara Bortolani, et al.Pediatric Blood & Cancer|April 12, 2018
Epidemiologic and clinical characteristics of nontransfusion-dependent thalassemia in the United StatesElliott Vichinsky, Alan Cohen, Alexis A Thompson, et al.Microorganisms|January 22, 2021
Study on Bacteria Isolates and Antimicrobial Resistance in Wildlife in Sicily, Southern ItalyDelia Gambino, Domenico Vicari, Maria Vitale, et al.Nano Letters|November 24, 2020
Multiorder Nonlinear Mixing in Metal Oxide NanoparticlesGabriel Campargue, Luca La Volpe, Gabriel Giardina, et al.Nutrients|November 27, 2025
Empowering Health Through Digital Lifelong Prevention: An Umbrella Review of Apps and Wearables for Nutritional ManagementMarta Giardina, Rosa Zarcone, Giulia Accardi, et al.Rheumatology (Oxford, England)|July 17, 2015
Potential involvement of IL-9 and Th9 cells in the pathogenesis of rheumatoid arthritisFrancesco Ciccia, Giuliana Guggino, Aroldo Rizzo, et al.Hematology (Amsterdam, Netherlands)|July 16, 2016
Reasons to Eliminate Umbilical Cord Blood Units before CryopreservationC Pafumi, M Farina, G Milone, et al.BMC Pharmacology & Toxicology|April 29, 2019
Characterization and preventability of adverse drug events as cause of emergency department visits: a prospective 1-year observational studyIvan Lo Giudice, Eleonora Mocciaro, Claudia Giardina, et al.Neurogenetics|March 27, 2019
Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS eraStefania Zampatti, Luca Colantoni, Claudia Strafella, et al.International Journal of Surgery (London, England)|January 2, 2014
Neuroendocrine breast cancer: retrospective analysis of 96 patients and review of literatureFrancesca Rovera, Matteo Lavazza, Stefano La Rosa, et al.Pageof 213