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Human Molecular Genetics|February 20, 2014
Mutation or knock-down of 17β-hydroxysteroid dehydrogenase type 10 cause loss of MRPP1 and impaired processing of mitochondrial heavy strand transcriptsAndrea J Deutschmann, Albert Amberger, Claudia Zavadil, et al.
Metabolites|April 26, 2024
Anaplerotic Therapy Using Triheptanoin in Two Brothers Suffering from Aconitase 2 DeficiencyMaximilian Penkl, Johannes A Mayr, René G Feichtinger, et al.
Neuromuscular Disorders : NMD|July 19, 2011
Deficiency of the mitochondrial phosphate carrier presenting as myopathy and cardiomyopathy in a family with three affected childrenJohannes A Mayr, Franz A Zimmermann, Rita Horváth, et al.
The British Journal of Radiology|July 20, 2019
Spinal metastasis: diagnosis, management and follow-upMahmud Mossa-Basha, Peter C Gerszten, Sten Myrehaug, et al.
Children (Basel, Switzerland)|July 2, 2021
Three Novel <i>EPCAM</i> Variants Causing Tufting Enteropathy in Three FamiliesHasret Ayyıldız Civan, Coleen Leitner, Iris Östreicher, et al.
Topics in Magnetic Resonance Imaging : TMRI|June 23, 2020
Communication and Team Interactions to Improve Patient Experiences, Quality of Care, and Throughput in MRIAmna A Ajam, Sana Tahir, Mina S Makary, et al.
Journal of Medical Radiation Sciences|April 19, 2016
Technical know-how in stereotactic ablative radiotherapy (SABR)Simon S Lo, Matthew Foote, Shankar Siva, et al.
World Journal of Hepatology|June 8, 2017
Strategies to tackle the challenges of external beam radiotherapy for liver tumorsMichael I Lock, Jonathan Klein, Hans T Chung, et al.
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