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Neuromuscular Disorders : NMD|March 1, 2003
Persistent over-expression of specific CC class chemokines correlates with macrophage and T-cell recruitment in mdx skeletal muscleJohn D Porter, Wei Guo, Anita P Merriam, et al.
Neuromuscular Disorders : NMD|March 1, 2003
Congenital myasthenic syndrome due to a novel missense mutation in the gene encoding choline acetyltransferaseCarolin Schmidt, Angela Abicht, Klaus Krampfl, et al.
Neuromuscular Disorders : NMD|March 1, 2003
Increased mitochondrial processing intermediates associated with three tRNA(Leu(UUR)) gene mutationsAtsuko Koga, Yasutoshi Koga, Yukihiro Akita, et al.
Neuromuscular Disorders : NMD|August 6, 2003
X-inactivation patterns in carriers of X-linked myotubular myopathyM Kristiansen, G P Knudsen, S M Tanner, et al.
Neuromuscular Disorders : NMD|June 14, 2022
Cognitive profiles and clinical factors in type III spinal muscular atrophy: a preliminary studySabrina Lenzoni, Carlo Semenza, Dalila Calligaro, et al.
Neuromuscular Disorders : NMD|February 8, 2011
Delayed presentation of invasive thymoma in myasthenia gravis: a case reportElizabeth C Galizia, Maria Elena Farrugia, Robert Swingler
Neuromuscular Disorders : NMD|October 19, 2010
Congenital fibre type disproportion associated with mutations in the tropomyosin 3 (TPM3) gene mimicking congenital myastheniaP Munot, D Lashley, H Jungbluth, et al.
Neuromuscular Disorders : NMD|December 1, 2010
Isolated dysphagia due to paraneoplastic myasthenic syndrome with anti-P/Q-type voltage-gated calcium-channel and anti-acetylcholine receptor antibodiesRoberto Fernandez-Torron, Juan Arcocha, Jose M López-Picazo, et al.
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