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Annals of Neurology|December 19, 2003
Diagnostic value of electromyography and muscle biopsy in arthrogryposis multiplex congenitaPeter B Kang, Hart G W Lidov, William S David, et al.
International Journal of Molecular Sciences|July 25, 2019
Increased mtDNA Abundance and Improved Function in Human Barth Syndrome Patient Fibroblasts Following AAV-<i>TAZ</i> Gene DeliverySilveli Suzuki-Hatano, Mughil Sriramvenugopal, Manash Ramanathan, et al.
FEBS Open Bio|November 7, 2020
Megf10 deficiency impairs skeletal muscle stem cell migration and muscle regenerationChengcheng Li, Dorianmarie Vargas-Franco, Madhurima Saha, et al.
BMC Musculoskeletal Disorders|November 27, 2007
LGMD2I in a North American populationPeter B Kang, Chris A Feener, Elicia Estrella, et al.
Journal of Translational Medicine|October 24, 2023
One episode of low intensity aerobic exercise prior to systemic AAV9 administration augments transgene delivery to the heart and skeletal muscleChristina A Pacak, Silveli Suzuki-Hatano, Fatemeh Khadir, et al.
Journal of Child Neurology|January 31, 2008
A case of congenital glycogen storage disease type IV with a novel GBE1 mutationG Praveen Raju, Hsin-Chang Li, Deeksha S Bali, et al.
The Journal of Experimental Medicine|October 6, 2005
The human macrophage mannose receptor directs Mycobacterium tuberculosis lipoarabinomannan-mediated phagosome biogenesisPeter B Kang, Abul K Azad, Jordi B Torrelles, et al.
Pediatric Transplantation|December 23, 2011
Rapid reversal of uremic neuropathy following renal transplantation in an adolescentDoreen T Ho, Nancy M Rodig, Heung B Kim, et al.
JAMA Neurology|March 5, 2014
Comparison of plasmapheresis and intravenous immunoglobulin as maintenance therapies for juvenile myasthenia gravisWendy K M Liew, Christine A Powell, Steven R Sloan, et al.
Neuromuscular Disorders : NMD|August 9, 2024
Three novel missense variants in two families with JAG2-associated limb-girdle muscular dystrophyLein Dofash, Krishnan Lyengar, Nolette Pereira, et al.
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