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Clinica Chimica Acta; International Journal of Clinical Chemistry|November 6, 2001
Overview of common inherited metabolic diseases in a Southern Chinese population of Hong KongN L Tang, J Hui, L K Law, et al.
International Journal of Obesity (2005)|February 18, 2011
Preadipocytes of type 2 diabetes subjects display an intrinsic gene expression profile of decreased differentiation capacityF H J van Tienen, C J H van der Kallen, P J Lindsey, et al.
Journal of the Neurological Sciences|April 1, 1988
Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's diseaseR J Wanders, H S Heymans, R B Schutgens, et al.
Human Molecular Genetics|February 12, 2014
Mitochondrial protein acetylation is driven by acetyl-CoA from fatty acid oxidationOlga Pougovkina, Heleen te Brinke, Rob Ofman, et al.
Journal of the American College of Cardiology|December 10, 2003
Phospholipid abnormalities in children with Barth syndromeMichael Schlame, Richard I Kelley, Annette Feigenbaum, et al.
Neuromuscular Disorders : NMD|July 23, 1998
Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch familiesP G Barth, R J Wanders, W Ruitenbeek, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|January 30, 2007
Time trends in the maximal uptake of FDG on PET scan during thoracic radiotherapy. A prospective study in locally advanced non-small cell lung cancer (NSCLC) patientsAngela van Baardwijk, Geert Bosmans, André Dekker, et al.
Journal of Medical Genetics|April 11, 2013
Rhizomelic chondrodysplasia punctata and cardiac pathologyIrene C Huffnagel, Sally-Ann B Clur, Annemieke M Bams-Mengerink, et al.
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