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Elife|May 30, 2023
Osteonecrosis in Gaucher disease in the era of multiple therapies: Biomarker set for risk stratification from a tertiary referral centerMohsen Basiri, Mohammad E Ghaffari, Jiapeng Ruan, et al.American Journal of Hematology|June 17, 2026
Cumulative Antigen Suppression Reduces Clonal Plasma Cell Evolution in Gaucher DiseaseNoor Ul Ain, Noffar Bar, Lilu Guo, et al.Journal of Neuromuscular Diseases|April 5, 2018
Treatment Algorithm for Infants Diagnosed with Spinal Muscular Atrophy through Newborn ScreeningJacqueline Glascock, Jacinda Sampson, Amanda Haidet-Phillips, et al.Lancet (London, England)|January 18, 2003
Intact fetal cells in maternal plasma: are they really there?Farideh Z Bischoff, Sinuhe Hahn, Kirby L Johnson, et al.Elife|August 16, 2022
Neuroinflammation in neuronopathic Gaucher disease: Role of microglia and NK cells, biomarkers, and response to substrate reduction therapyChandra Sekhar Boddupalli, Shiny Nair, Glenn Belinsky, et al.Molecular Genetics and Metabolism|June 18, 2010
Inhibition of glycogen biosynthesis via mTORC1 suppression as an adjunct therapy for Pompe diseaseKaren M Ashe, Kristin M Taylor, Qiuming Chu, et al.Molecular Cancer Therapeutics|March 1, 2006
Protein tyrosine phosphatase PRL-3 in malignant cells and endothelial cells: expression and functionCecile Rouleau, Andre Roy, Thia St Martin, et al.Genome Medicine|December 17, 2025
Genetic liability to psoriasis predicts severe disease outcomesJake R Saklatvala, Samuel Lessard, Maris Teder-Laving, et al.Nature|January 18, 2023
FinnGen provides genetic insights from a well-phenotyped isolated populationMitja I Kurki, Juha Karjalainen, Priit Palta, et al.Pageof 2