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Archives of Biochemistry and Biophysics|September 11, 1991
Peroxisomal fatty acid beta-oxidation in HepG2 cellsP A Watkins, E V Ferrell, J I Pedersen, et al.Pediatric Research|March 1, 1990
Aberrant subcellular localization of peroxisomal 3-ketoacyl-CoA thiolase in the Zellweger syndrome and rhizomelic chondrodysplasia punctataA Balfe, G Hoefler, W W Chen, et al.Prenatal Diagnosis|October 1, 1988
Prenatal diagnosis of rhizomelic chondrodysplasia punctataS Hoefler, G Hoefler, A B Moser, et al.European Journal of Gastroenterology & Hepatology|February 18, 2005
Critical issues in the identification and management of patients with hereditary non-polyposis colorectal cancerC Lackner, G HoeflerThe Journal of Pediatrics|May 1, 1988
Biochemical abnormalities in rhizomelic chondrodysplasia punctataG Hoefler, S Hoefler, P A Watkins, et al.International Journal of Experimental Pathology|April 12, 2001
Metabolic cardiomyopathiesB Guertl, C Noehammer, G HoeflerNeurology|July 1, 1988
Neonatal seizures and retardation in a girl with biochemical features of X-linked adrenoleukodystrophy: a possible new peroxisomal disease entityS Naidu, G Hoefler, P A Watkins, et al.Biochimie|January 1, 1993
Peroxisomal oxidation of the steroid side chain in bile acid formationJ I PedersenAmerican Journal of Human Genetics|January 23, 1999
Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basisE G van Grunsven, E van Berkel, P A Mooijer, et al.Biochimica Et Biophysica Acta|May 29, 1985
25-Hydroxylation of 1 alpha-hydroxyvitamin D-3 in rat and human liverK Saarem, J I PedersenPageof 23