Showing results (851-860 of 1,321) with videos related to

Sort By:
Pageof 133
Pediatric Research|August 6, 2000
Heterozygosity for the common LCHAD mutation (1528g>C) is not a major cause of HELLP syndrome and the prevalence of the mutation in the Dutch population is lowM E den Boer, L Ijlst, F A Wijburg, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1987
Prenatal diagnosis of Zellweger syndrome by measurement of very long chain fatty acid (C26:0) beta-oxidation in cultured chorionic villous fibroblasts: implications for early diagnosis of other peroxisomal disordersR J Wanders, M J van Wijland, C W van Roermund, et al.
Plos One|August 23, 2012
Bezafibrate for X-linked adrenoleukodystrophyMarc Engelen, Luc Tran, Rob Ofman, et al.
The British Journal of Nutrition|August 2, 2012
The effects of bulking, viscous and gel-forming dietary fibres on satiationAnne J Wanders, Melliana C Jonathan, Joost J G C van den Borne, et al.
American Journal of Nephrology|June 18, 2005
Intra-familial clinical heterogeneity: absence of genotype-phenotype correlation in primary hyperoxaluria type 1 in IsraelYaacov Frishberg, Choni Rinat, Adel Shalata, et al.
Clinical Chemistry|December 12, 2007
Bloodspot assay using HPLC-tandem mass spectrometry for detection of Barth syndromeWillem Kulik, Henk van Lenthe, Femke S Stet, et al.
British Journal of Cancer|April 3, 1999
Phase I study of Carzelesin (U-80,244) given (4-weekly) by intravenous bolus scheduleA Awada, C J Punt, M J Piccart, et al.
Clinical and Translational Gastroenterology|June 28, 2013
Human enterovirus species B in ileocecal Crohn's diseaseNiklas Nyström, Tove Berg, Elin Lundin, et al.
Human Molecular Genetics|May 20, 1999
Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disordersN Shimozawa, Y Suzuki, Z Zhang, et al.
Breast Cancer Research and Treatment|December 25, 2016
Volumetric breast density affects performance of digital screening mammographyJohanna O P Wanders, Katharina Holland, Wouter B Veldhuis, et al.
Pageof 133