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Molecular Genetics and Metabolism|August 5, 2000
Hyperphenylalaninemia and 7-pterin excretion associated with mutations in 4a-hydroxy-tetrahydrobiopterin dehydratase/DCoH: analysis of enzyme activity in intestinal biopsiesJ E Ayling, S W Bailey, S R Boerth, et al.Journal of Inherited Metabolic Disease|October 16, 2009
Novel mutation affecting the pterin-binding site of PTS gene and review of PTS mutations in Thai patients with 6-pyruvoyltetrahydropterin synthase deficiencyN Vatanavicharn, C Kuptanon, S Liammongkolkul, et al.Pediatric Radiology|January 1, 1982
The prenatal ultrasonic diagnosis of urethral obstruction and diverticulum of the urinary bladderJ Shalev, Y Itzchak, H Blau, et al.Traffic (Copenhagen, Denmark)|September 6, 2005
Cyclase-associated protein is essential for the functioning of the endo-lysosomal system and provides a link to the actin cytoskeletonHameeda Sultana, Francisco Rivero, Rosemarie Blau-Wasser, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 12, 2014
Increasing nontuberculous mycobacteria infection in cystic fibrosisOphir Bar-On, Huda Mussaffi, Meir Mei-Zahav, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 1, 2016
Reversible airway obstruction in cystic fibrosis: Common, but not associated with characteristics of asthmaHagit Levine, Malena Cohen-Cymberknoh, Nitai Klein, et al.Journal of the American Chemical Society|September 3, 2008
Ordered DNA wrapping switches on luminescence in single-walled nanotube dispersionsHelen Cathcart, Valeria Nicolosi, J Marguerite Hughes, et al.Pediatric Research|December 1, 1992
Atypical (mild) forms of dihydropteridine reductase deficiency: neurochemical evaluation and mutation detectionN Blau, C W Heizmann, W Sperl, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 7, 2012
Therapeutic angiogenesis due to balanced single-vector delivery of VEGF and PDGF-BBAndrea Banfi, Georges von Degenfeld, Roberto Gianni-Barrera, et al.Prenatal Diagnosis|July 29, 2005
Pre- and postnatal diagnosis of tyrosine hydroxylase deficiencyLisbeth Birk Møller, Anne Romstad, Marianne Paulsen, et al.Pageof 236