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The New England Journal of Medicine|June 7, 2013
Central precocious puberty caused by mutations in the imprinted gene MKRN3Ana Paula Abreu, Andrew Dauber, Delanie B Macedo, et al.Bioorganic & Medicinal Chemistry Letters|March 20, 2012
Discovery of new piperidine amide triazolobenzodiazepinones as intestinal-selective CCK1 receptor agonistsKimberly O Cameron, Elena E Beretta, Yue Chen, et al.Bioorganic & Medicinal Chemistry Letters|September 21, 2010
Discovery of N-benzyl-2-[(4S)-4-(1H-indol-3-ylmethyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]-N-isopropylacetamide, an orally active, gut-selective CCK1 receptor agonist for the potential treatment of obesityRichard L Elliott, Kimberly O Cameron, Janice E Chin, et al.Journal of Neurology|April 28, 2026
X-linked Emery-Dreifuss muscular dystrophy: a multicenter, Italian, cohort studyA Elkoush, R Giossi, G Gadaleta, et al.The Journal of Clinical Endocrinology and Metabolism|December 31, 2020
Genotype-Phenotype Correlations in Central Precocious Puberty Caused by MKRN3 MutationsCarlos Eduardo Seraphim, Ana Pinheiro Machado Canton, Luciana Montenegro, et al.Orphanet Journal of Rare Diseases|July 9, 2016
MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patientsC Fiorillo, G Astrea, M Savarese, et al.Pageof 37