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International Journal of Molecular Sciences|January 27, 2024
Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter StudyBenedetta Cavirani, Carlotta Spagnoli, Stefano Giuseppe Caraffi, et al.
The Journal of Clinical Investigation|April 4, 2007
Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humansLiesbeth Van Wesenbeeck, Paul R Odgren, Fraser P Coxon, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 12, 2011
A nonsynonymous TNFRSF11A variation increases NFκB activity and the severity of Paget's diseaseFernando Gianfrancesco, Domenico Rendina, Marco Di Stefano, et al.
Genetics, Selection, Evolution : GSE|August 5, 2015
Genetic diversity of Italian goat breeds assessed with a medium-density SNP chipLetizia Nicoloso, Lorenzo Bomba, Licia Colli, et al.
Italian Journal of Pediatrics|December 18, 2014
Multiple sulfatase deficiency with neonatal manifestationLivia Garavelli, Lucia Santoro, Alexandra Iori, et al.
Blood Advances|February 2, 2018
Phase 2 trial of a multivalent WT1 peptide vaccine (galinpepimut-S) in acute myeloid leukemiaPeter G Maslak, Tao Dao, Yvette Bernal, et al.
Journal of Neurotrauma|December 29, 2020
Predicting Outcome of Acquired Brain Injury by the Evolution of Paroxysmal Sympathetic Hyperactivity SignsLucia F Lucca, Antonio De Tanti, Francesca Cava, et al.
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