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Human Genetics|November 7, 2015
Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humansHanan E Shamseldin, Laura L Smith, Amal Kentab, et al.
Ultrastructural Pathology|July 19, 2018
The histological spectrum of tubulo-reticular inclusion positive renal biopsies: a tertiary hospital experience and review of the literatureHala Kfoury, Mohammed Mubarak, Abd Assalam Qannus, et al.
Ophthalmic Genetics|February 6, 2016
Duane retraction syndrome in a patient with Duchenne muscular dystrophyThomas M Bosley, Mustafa A Salih, Hisham Alkhalidi, et al.
Journal of Medical Genetics|April 14, 2012
Genomic analysis of mitochondrial diseases in a consanguineous population reveals novel candidate disease genesHanan E Shamseldin, Muneera Alshammari, Tarfa Al-Sheddi, et al.
Oxidative Medicine and Cellular Longevity|June 6, 2012
Metformin rescues the myocardium from doxorubicin-induced energy starvation and mitochondrial damage in ratsAbdelkader E Ashour, Mohamed M Sayed-Ahmed, Adel R Abd-Allah, et al.
Journal of Neurosurgery. Spine|July 21, 2018
In vivo assessment of spinal cord elasticity using shear wave ultrasound in dogsAmro Al-Habib, Abdulrahman Albakr, Abdullah Al Towim, et al.
Case Reports in Oncology|April 26, 2024
A New Sarcoma Shortly after Treatment for High-Grade Glioma with Adjuvant Chemoradiation: A Case ReportAbdossalam M Madkhali, Hasah F Alaluan, Mohammed H Alnajeim, et al.
Scientific Reports|June 3, 2020
Endothelial dysfunction in nonalcoholic steatohepatitis with low cardiac disease riskWaleed Al-Hamoudi, Amani Alsadoon, Mazen Hassanian, et al.
Genetic Testing and Molecular Biomarkers|December 17, 2021
Exome Sequencing Reveals Novel <i>TTN</i> Variants in Saudi Patients with Congenital TitinopathiesMustafa A Salih, Muddathir H Hamad, Marco Savarese, et al.
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