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Movement Disorders : Official Journal of the Movement Disorder Society|April 18, 2012
A new phenotype of brain iron accumulation with dystonia, optic atrophy, and peripheral neuropathyRita Horvath, Elke Holinski-Feder, Vivienne C M Neeve, et al.Blood Reviews|November 29, 2025
CARing about autoimmune disorders. Use of chimeric antigen receptor engineered T-cells in autoimmune diseasesAdrian-Bogdan Tigu, Madalina Nistor, Diana Gulei, et al.Genome Research|May 1, 1997
A 1.1-Mb transcript map of the hereditary hemochromatosis locusD A Ruddy, G S Kronmal, V K Lee, et al.JACC. Advances|February 19, 2026
Cardiac Rehabilitation Utilization Among Veterans: A Sex-Based AnalysisMerilyn S Varghese, Ling Han, Parul U Gandhi, et al.Journal of Cellular and Molecular Medicine|September 5, 2023
Design and preclinical testing of an anti-CD41 CAR T cell for the treatment of acute megakaryoblastic leukaemiaAdrian Bogdan Tigu, Catalin Sorin Constantinescu, Patric Teodorescu, et al.Cell Reports|June 28, 2016
MEIS2 Is an Oncogenic Partner in AML1-ETO-Positive AMLNaidu M Vegi, Josef Klappacher, Franz Oswald, et al.Plos One|April 15, 2017
New insights into valve-related intramural and intracellular bacterial diversity in infective endocarditisAndreas Oberbach, Nadine Schlichting, Stefan Feder, et al.Brain : a Journal of Neurology|September 13, 2022
Methylation of the 4q35 D4Z4 repeat defines disease status in facioscapulohumeral muscular dystrophyHannes Erdmann, Florentine Scharf, Stefanie Gehling, et al.Pediatric Pulmonology|January 9, 2025
Genetic Concordance of Staphylococcus aureus From Oropharyngeal and Sputum Cultures in People With Cystic FibrosisChristian F Zirbes, Andries Feder, Anthony J Pamatmat, et al.JNCI Cancer Spectrum|April 14, 2026
Effect of a polygenic risk score in patients with late-onset, early-onset, familial, or hereditary colorectal cancerHannah Klinkhammer, Isabel Spier, Claudia Perne, et al.Pageof 224