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Orphanet Journal of Rare Diseases|October 31, 2012
The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectivesAnnet M Bosch, Kevin Stroek, Nico G Abeling, et al.Neuromuscular Disorders : NMD|June 21, 2014
Rhabdomyolysis: review of the literatureR Zutt, A J van der Kooi, G E Linthorst, et al.Neuropediatrics|June 15, 2006
Pitfall in metabolic screening in a patient with fatal peroxisomal beta-oxidation defectH Rosewich, H R Waterham, R J A Wanders, et al.The Analyst|November 26, 2014
A microfluidic interface for the culture and sampling of adiponectin from primary adipocytesLeah A Godwin, Jessica C Brooks, Lauren D Hoepfner, et al.Public Health|June 27, 2025
Association between police funding and community firearm violence incidence in 61 US cities, 2015-2022Anita Wamakima, Leah E Roberts, Siena Wanders, et al.American Journal of Medical Genetics. Part A|August 5, 2010
A mutation in PEX19 causes a severe clinical phenotype in a patient with peroxisomal biogenesis disorderSarar Mohamed, Ebtisam El-Meleagy, Abdelhaleem Nasr, et al.European Journal of Biochemistry|September 15, 1983
Properties of carbamoyl-phosphate synthetase (ammonia) in rat-liver mitochondria made permeable with tolueneC Lof, M Cohen, L P Vermeulen, et al.Nederlands Tijdschrift Voor Geneeskunde|August 23, 2006
[From gene to disease; primary hyperoxaluria type I caused by mutations in the AGXT gene]C S van Woerden, J W Groothof, R J A Wanders, et al.Journal of Lipid Research|February 20, 1998
Phytanic acid and pristanic acid are oxidized by sequential peroxisomal and mitochondrial reactions in cultured fibroblastsN M Verhoeven, D S Roe, R M Kok, et al.Journal of Cell Science|January 20, 2004
Mevalonate kinase is a cytosolic enzyme in humansSietske Hogenboom, John J M Tuyp, Marc Espeel, et al.Pageof 132