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Clinical Breast Cancer|March 20, 2010
Phase III trials of eribulin mesylate (E7389) in extensively pretreated patients with locally recurrent or metastatic breast cancerChris Twelves, Javier Cortes, Linda T Vahdat, et al.Annals of Oncology : Official Journal of the European Society for Medical Oncology|June 12, 2001
Activity of the dolastatin analogue, LU103793, in malignant melanomaJ Smyth, M E Boneterre, J Schellens, et al.American Journal of Human Genetics|May 1, 1996
Molecular characterization of mitochondrial trifunctional protein deficiency: formation of the enzyme complex is important for stabilization of both alpha- and beta-subunitsS Ushikubo, T Aoyama, T Kamijo, et al.Genomics|April 1, 1996
3-Hydroxy-3-methylglutaryl CoA lyase (HL): mouse and human HL gene (HMGCL) cloning and detection of large gene deletions in two unrelated HL-deficient patientsS P Wang, M F Robert, K M Gibson, et al.Pediatric Neurology|May 13, 2009
Mitochondrial trifunctional protein deficiency with recurrent rhabdomyolysisOded Scheuerman, Ronald J A Wanders, Hans R Waterham, et al.Biological Psychiatry|March 21, 2001
Significantly reduced docosahexaenoic and docosapentaenoic acid concentrations in erythrocyte membranes from schizophrenic patients compared with a carefully matched control groupJ Assies, R Lieverse, P Vreken, et al.Journal of Inherited Metabolic Disease|July 17, 1999
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)P G Barth, R J Wanders, P Vreken, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 21, 2014
Food withdrawal lowers energy expenditure and induces inactivity in long-chain fatty acid oxidation-deficient mouse modelsEugene F Diekman, Michel van Weeghel, Ronald J A Wanders, et al.Acta Radiologica (Stockholm, Sweden : 1987)|September 27, 2003
Effect of granulocyte colony-stimulating factor (G-CSF)-supported chemotherapy on MR imaging of normal red bone marrow in breast cancer patients with focal bone metastasesI Ciray, H Lindman, G K O Aström, et al.Pediatric Neurology|August 11, 2004
PEX1 deficiency presenting as Leber congenital amaurosisHelen M Michelakakis, Dimitrios I Zafeiriou, Marina S Moraitou, et al.Pageof 132