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Archives De L'Institut Pasteur De Tunis|April 25, 2009
Novel mutations in LAMA2 gene responsible for a severe phenotype of congenital muscular dystrophy in two Tunisian familiesN Louhichi, P Richard, C H Triki, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 27, 2009
Hypertension of Kcnmb1-/- is linked to deficient K secretion and aldosteronismP Richard Grimm, Debra L Irsik, Deann C Settles, et al.
Brain, Behavior, and Immunity|February 8, 2025
Regional brain structural alterations in reward and salience networks in asthmaDanielle Carrol, William W Busse, Corrina J Frye, et al.
JOR Spine|October 2, 2023
Epidemiology of Modic changes in dogs: Prevalence, possible risk factors, and association with spinal phenotypesMartijn Beukers, Guy C M Grinwis, Johannes C M Vernooij, et al.
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