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Neuromuscular Disorders : NMD|August 30, 2022
Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotypeG Diane Shelton, Katie M Minor, Natassia M Vieira, et al.
Neuromuscular Disorders : NMD|October 9, 2022
PURA syndrome: neuromuscular junction manifestations with potential therapeutic implicationsHebah Qashqari, Vanda McNiven, Hernan Gonorazky, et al.
Neuromuscular Disorders : NMD|December 27, 2021
Electrocardiographic prediction of late gadolinium enhancement on cardiac magnetic resonance in Becker muscular dystrophyJeffrey S Bennett, Anna N Kamp, Linda H Cripe, et al.
Neuromuscular Disorders : NMD|May 20, 2011
Variation of serum creatine kinase (CK) levels and prevalence of persistent hyperCKemia in a Norwegian normal population. The Tromsø StudyHallvard Lilleng, Karin Abeler, Stein H Johnsen, et al.
Neuromuscular Disorders : NMD|May 3, 2011
Telethonin-deficiency initially presenting as a congenital muscular dystrophyAna Ferreiro, Monica Mezmezian, Montse Olivé, et al.
Neuromuscular Disorders : NMD|July 5, 2011
Scoliosis surgery in a patient with "de novo" myosin storage myopathyXenia Stalpers, Aad Verrips, Jan Braakhekke, et al.
Neuromuscular Disorders : NMD|June 21, 2011
A study of FHL1, BAG3, MATR3, PTRF and TCAP in Australian muscular dystrophy patientsLeigh B Waddell, Jenny Tran, Xi F Zheng, et al.
Neuromuscular Disorders : NMD|July 5, 2011
Serum matrix metalloproteinase-9 (MMP-9) as a biomarker for monitoring disease progression in Duchenne muscular dystrophy (DMD)V D Nadarajah, M van Putten, A Chaouch, et al.
Neuromuscular Disorders : NMD|April 13, 2011
Endplate structure and parameters of neuromuscular transmission in sporadic centronuclear myopathy associated with myastheniaTeerin Liewluck, Xin-Ming Shen, Margherita Milone, et al.
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