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Journal of Internal Medicine|March 19, 2011
Nonalcoholic fatty liver disease: an independent risk factor for colorectal neoplasiaA Stadlmayr, E Aigner, B Steger, et al.
Journal of Inherited Metabolic Disease|May 7, 2019
Mitochondrial DNA mutation analysis from exome sequencing-A more holistic approach in diagnostics of suspected mitochondrial diseaseMatias Wagner, Riccardo Berutti, Bettina Lorenz-Depiereux, et al.
European Journal of Medical Genetics|July 6, 2016
MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosumIngrid Bader, E Decker, J A Mayr, et al.
International Journal of Radiation Oncology, Biology, Physics|July 28, 2009
Translating response during therapy into ultimate treatment outcome: a personalized 4-dimensional MRI tumor volumetric regression approach in cervical cancerNina A Mayr, Jian Z Wang, Simon S Lo, et al.
Journal of General Internal Medicine|December 12, 2023
Mortality Among Older Medical Patients at Flagship Hospitals and Their AffiliatesSiddharth Jain, Paul R Rosenbaum, Joseph G Reiter, et al.
Mitochondrion|July 12, 2017
LYRM7 - associated complex III deficiency: A clinical, molecular genetic, MR tomographic, and biochemical studyMaja Hempel, Laura S Kremer, Konstantinos Tsiakas, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Congenital cataract, muscular hypotonia, developmental delay and sensorineural hearing loss associated with a defect in copper metabolismR Horváth, P Freisinger, R Rubio, et al.
Medical Care|July 4, 2019
Comparing Resource Use in Medical Admissions of Children With Complex Chronic ConditionsJeffrey H Silber, Paul R Rosenbaum, Samuel D Pimentel, et al.
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