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Nature Communications|April 8, 2026
RPS19 and RPL5 haploinsufficient models reveal divergent ribosomal subunit controls of fetal hematopoiesisYuefeng Tang, Te Ling, Rashid Mehmood, et al.Human Mutation|October 21, 2010
The ribosomal basis of Diamond-Blackfan Anemia: mutation and database updateIlenia Boria, Emanuela Garelli, Hanna T Gazda, et al.Archives of Neurology|November 10, 2010
Temporoparietal hypometabolism in frontotemporal lobar degeneration and associated imaging diagnostic errorsKyle B Womack, Ramon Diaz-Arrastia, Howard J Aizenstein, et al.The Lancet. Haematology|May 2, 2024
Diagnosis, treatment, and surveillance of Diamond-Blackfan anaemia syndrome: international consensus statementMarcin W Wlodarski, Adrianna Vlachos, Jason E Farrar, et al.The Journal of Rheumatology|April 17, 2015
Dissecting the heterogeneity of macrophage activation syndrome complicating systemic juvenile idiopathic arthritisFrancesca Minoia, Sergio Davì, AnnaCarin Horne, et al.Nature Communications|February 27, 2021
Distinct genetic pathways define pre-malignant versus compensatory clonal hematopoiesis in Shwachman-Diamond syndromeAlyssa L Kennedy, Kasiani C Myers, James Bowman, et al.American Journal of Human Genetics|December 4, 2018
The Genetic Landscape of Diamond-Blackfan AnemiaJacob C Ulirsch, Jeffrey M Verboon, Shideh Kazerounian, et al.Pageof 33