Showing results (631-640 of 944) with videos related to
Sort By:
Pageof 95
Molecular Genetics and Metabolism|May 17, 2017
Partial rescue of neuropathology in the murine model of PKU following administration of recombinant phenylalanine ammonia lyase (pegvaliase)Marc Goldfinger, William L Zeile, Carley R Corado, et al.Acta Physiologica (Oxford, England)|February 2, 2011
Opposing effects of NaCl restriction and carbohydrate loading on urine volume in diabetic ratsH A O'Neill, T-H Kwon, T Ring, et al.Neurourology and Urodynamics|July 1, 2004
Hypoxia inhibits human bladder smooth muscle cell proliferation: a potential mechanism of bladder dysfunctionD J Galvin, R W G Watson, A O'Neill, et al.The American Surgeon|January 10, 2001
Twenty-five-year surgical experience with pheochromocytoma in childrenV S Reddy, J A O'Neill, G W Holcomb, et al.Diabetes, Obesity & Metabolism|February 10, 2021
A randomized, placebo-controlled trial to assess the efficacy and safety of sitagliptin in Japanese patients with type 2 diabetes and inadequate glycaemic control on ipragliflozinYutaka Seino, Kohei Kaku, Takashi Kadowaki, et al.Pediatric Research|February 1, 2012
Intrathecal recombinant human 4-sulfatase reduces accumulation of glycosaminoglycans in dura of mucopolysaccharidosis VI catsDyane Auclair, John Finnie, Steven U Walkley, et al.Diabetes, Obesity & Metabolism|May 25, 2021
Efficacy and safety of ipragliflozin in Japanese patients with type 2 diabetes and inadequate glycaemic control on sitagliptinKohei Kaku, Takashi Kadowaki, Yutaka Seino, et al.Carbohydrate Research|February 1, 2003
Primary structure of the 2-O-methyl-alpha-L-fucose-containing side chain of the pectic polysaccharide, rhamnogalacturonan IIJohn N Glushka, Mark Terrell, William S York, et al.American Journal of Epidemiology|April 1, 2005
Polygenic effects and cigarette smoking account for a portion of the familial aggregation of nuclear sclerosisAlison P Klein, Priya Duggal, Kristine E Lee, et al.Clinical and Translational Science|June 2, 2021
Dose selection for intracerebroventricular cerliponase alfa in children with CLN2 disease, translation from animal to human in a rare genetic diseaseKevin Hammon, Greg de Hart, Brian R Vuillemenot, et al.Pageof 95