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Molecular Genetics and Metabolism|September 20, 2000
Human acid ceramidase gene: novel mutations in Farber diseaseZ Zhang, A K Mandal, A Mital, et al.American Journal of Medical Genetics|May 17, 1996
Urinary bile acids and peroxisomal bifunctional enzyme deficiencyM R Natowicz, J E Evans, R I Kelley, et al.Science (New York, N.Y.)|May 6, 2006
Conjunctive representation of position, direction, and velocity in entorhinal cortexFrancesca Sargolini, Marianne Fyhn, Torkel Hafting, et al.Acta Neuropathologica|January 1, 1987
Neuronal lipidosis and neuroaxonal dystrophy in cerebro-hepato-renal (Zellweger) syndromeJ M Powers, R C Tummons, A B Moser, et al.Optics Express|May 4, 2016
Compact quantum cascade laser based quartz-enhanced photoacoustic spectroscopy sensor system for detection of carbon disulfideJohannes P Waclawek, Harald Moser, Bernhard LendlPeerj|September 5, 2015
Modeling absolute differences in life expectancy with a censored skew-normal regression approachAndré Moser, Kerri Clough-Gorr, Marcel ZwahlenClimatic Change|March 28, 2020
The long arm of climate change: societal teleconnections and the future of climate change impacts studiesSusanne C Moser, Juliette A Finzi HartEbiomedicine|January 10, 2021
Understanding and treating paediatric hearing impairmentChristian Wrobel, Maria-Patapia Zafeiriou, Tobias MoserJournal of Inherited Metabolic Disease|May 10, 2002
Lipid status and long-chain polyunsaturated fatty acid concentrations in adults and adolescents with phenylketonuria on phenylalanine-restricted dietK Moseley, R Koch, A B MoserPageof 1,148