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Human Genetics|October 1, 1991
X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetusL Van Maldergem, M Espeel, F Roels, et al.
International Journal of Radiation Oncology, Biology, Physics|November 13, 2007
Time trends in nodal volumes and motion during radiotherapy for patients with stage III non-small-cell lung cancerGeert Bosmans, Angela van Baardwijk, André Dekker, et al.
Journal of Lipid Research|December 6, 2001
Identification of the peroxisomal beta-oxidation enzymes involved in the biosynthesis of docosahexaenoic acidS Ferdinandusse, S Denis, P A Mooijer, et al.
Virchows Archiv : an International Journal of Pathology|July 6, 2000
Hepatic peroxisomes in isolated hyperpipecolic acidaemia: evidence supporting its classification as a single peroxisomal enzyme deficiencyI Kerckaert, B T Poll-The, M Espeel, et al.
Biochimica Et Biophysica Acta|January 9, 1985
The cerebro-hepato-renal (Zellweger) syndrome. Impaired de novo biosynthesis of plasmalogens in cultured skin fibroblastsG Schrakamp, R B Schutgens, R J Wanders, et al.
The American Journal of Clinical Nutrition|August 11, 2017
Dietary fatty acid intake after myocardial infarction: a theoretical substitution analysis of the Alpha Omega CohortFamke J M Mölenberg, Janette de Goede, Anne J Wanders, et al.
Psychological Medicine|November 28, 2017
Person-fit feedback on inconsistent symptom reports in clinical depression careRob B K Wanders, Rob R Meijer, Henricus G Ruhé, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 4, 2012
αB-Crystallin regulates expansion of CD11b⁺Gr-1⁺ immature myeloid cells during tumor progressionLothar C Dieterich, Petter Schiller, Hua Huang, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications|September 24, 1998
Rapid stable isotope dilution analysis of very-long-chain fatty acids, pristanic acid and phytanic acid using gas chromatography-electron impact mass spectrometryP Vreken, A E van Lint, A H Bootsma, et al.
Human Mutation|October 30, 2010
Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorderMerel S Ebberink, Petra A W Mooijer, Jeannette Gootjes, et al.
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