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Molecular Genetics and Metabolism|May 15, 2001
Mutation analysis of the MCM gene in Israeli patients with mut(0) diseaseI Berger, A Shaag, Y Anikster, et al.
European Journal of Pediatrics|September 15, 1999
Metabolic stroke in isolated 3-methylcrotonyl-CoA carboxylase deficiencyC Steen, E R Baumgartner, M Duran, et al.
Journal of Inherited Metabolic Disease|October 13, 2001
CblC/D defect combined with haemodynamically highly relevant VSDM Tomaske, A Bosk, M K Heinemann, et al.
Journal of Inherited Metabolic Disease|May 16, 2020
Organic acidurias: Major gaps, new challenges, and a yet unfulfilled promiseBianca Dimitrov, Femke Molema, Monique Williams, et al.
Journal of Inherited Metabolic Disease|March 13, 2015
Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelinesMartina Huemer, Viktor Kožich, Piero Rinaldo, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 18, 2000
Plasmid vaccine expressing granulocyte-macrophage colony-stimulating factor attracts infiltrates including immature dendritic cells into injected musclesD Haddad, J Ramprakash, M Sedegah, et al.
Drug and Alcohol Dependence|June 29, 2013
Differences in self-reported and behavioral measures of impulsivity in recreational and dependent cocaine usersMatthias Vonmoos, Lea M Hulka, Katrin H Preller, et al.
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