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Neuromuscular Disorders : NMD|November 15, 2011
Transgenic inactivation of murine myostatin does not decrease the severity of disease in a model of Spinal Muscular AtrophyHansjörg Rindt, Desire M Buckley, Spencer M Vale, et al.
Neuromuscular Disorders : NMD|May 27, 2009
Beneficial effect of rituximab monotherapy in multifocal motor neuropathyKarl Stieglbauer, Raffi Topakian, Georg Hinterberger, et al.
Neuromuscular Disorders : NMD|May 29, 2009
Basement membrane remodelling and segmental fibrosis in sporadic inclusion body myositisK Doppler, M Mittelbronn, A Lindner, et al.
Neuromuscular Disorders : NMD|May 30, 2009
Expression of apoptosis related proteins in normal and diseased muscle: a possible role for Bcl-2 in protection of striated muscleOlof Danielsson, Cathrine Nilsson, Björn Lindvall, et al.
Neuromuscular Disorders : NMD|May 30, 2009
The second wind phenomenon in very young McArdle's patientsMargarita Pérez, Jonatan R Ruiz, María Fernández Del Valle, et al.
Neuromuscular Disorders : NMD|February 24, 2009
Clinical and audiological follow up of a family with the 8363G>A mutation in the mitochondrial DNARoberto DiFabio, Filippo M Santorelli, Giuseppe Nola, et al.
Neuromuscular Disorders : NMD|June 26, 2009
Severe nemaline myopathy associated with consecutive mutations E74D and H75Y on a single ACTA1 alleleNatalia Garcia-Angarita, Janbernd Kirschner, Mandy Heiliger, et al.
Neuromuscular Disorders : NMD|June 26, 2009
A TPM3 mutation causing cap myopathyAndre Maues De Paula, Jerome Franques, Carla Fernandez, et al.
Neuromuscular Disorders : NMD|January 10, 2012
Partial tandem duplication of mtDNA-tRNA(Phe) impairs mtDNA translation in late-onset mitochondrial myopathyPaola Arzuffi, Costanza Lamperti, Erika Fernandez-Vizarra, et al.
Neuromuscular Disorders : NMD|February 21, 2012
Experimental validation of in silico predicted KCNA1, KCNA2, KCNA6 and KCNQ2 genes for association studies of peripheral nerve hyperexcitability syndrome in Jack Russell TerriersMario Van Poucke, An E Vanhaesebrouck, Luc J Peelman, et al.
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