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Neuromuscular Disorders : NMD|September 18, 2012
Whole-Body muscle MRI in a series of patients with congenital myopathy related to TPM2 gene mutationsMohamed Jarraya, Susana Quijano-Roy, Nicole Monnier, et al.Neuromuscular Disorders : NMD|July 13, 2012
Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvementT Cullup, P J Lamont, S Cirak, et al.Neuromuscular Disorders : NMD|July 10, 2012
The inside and out of dystroglycan post-translational modificationChris J Moore, Steve J WinderNeuromuscular Disorders : NMD|August 26, 1998
Consequences of the combined deficiency in dystrophin and utrophin on the mechanical properties and myosin composition of some limb and respiratory muscles of the mouseN Deconinck, J A Rafael, G Beckers-Bleukx, et al.Neuromuscular Disorders : NMD|August 26, 1998
Molecular genetics and pathogenesis of Friedreich ataxiaM PandolfoNeuromuscular Disorders : NMD|July 23, 1998
Distal myopathy with rimmed vacuolesI Nonaka, N Murakami, Y Suzuki, et al.Neuromuscular Disorders : NMD|March 23, 2010
WITHDRAWN: Nemaline myopathy presenting as a stiff babyRakesh Kumar Jain, Sandeep JayawantNeuromuscular Disorders : NMD|January 31, 2015
A novel dynamin-2 gene mutation associated with a late-onset centronuclear myopathy with necklace fibresOlivera Casar-Borota, Johan Jacobsson, Rolf Libelius, et al.Neuromuscular Disorders : NMD|January 24, 2015
Abnormal sodium current properties contribute to cardiac electrical and contractile dysfunction in a mouse model of myotonic dystrophy type 1Vincent Algalarrondo, Karim Wahbi, Frédéric Sebag, et al.Neuromuscular Disorders : NMD|July 30, 2022
Metrics of progression and prognosis in untreated adults with thymidine kinase 2 deficiency: An observational studyCristina Domínguez-González, Ana Hernández-Voth, Carlos Pablo de Fuenmayor-Fernández de la Hoz, et al.Pageof 340