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Neuromuscular Disorders : NMD|December 9, 2009
Physical characteristics and applicability of standard assessment methods in a total population of spinal muscular atrophy type II patientsU Werlauff, B F Steffensen, S Bertelsen, et al.
Neuromuscular Disorders : NMD|April 20, 2019
Wrist drop in an arcade dancing game: Unusual sudden bilateral radial palsyGabriel Cea, Juan Pablo Contreras, Shirley Aguilar, et al.
Neuromuscular Disorders : NMD|September 23, 2018
Non-compaction cardiomyopathy and early respiratory failure in an adult symptomatic female carrier of centronuclear myopathy caused by a MTM1 mutationJ García-García, M A Fernández-García, P Blanco-Arias, et al.
Neuromuscular Disorders : NMD|October 6, 2018
Characterization of Australian Labradoodle dystrophinopathyStephanie M Shrader, SeungWoo Jung, Thomas S Denney, et al.
Neuromuscular Disorders : NMD|September 3, 2018
A new severe mutation in the SLC5A7 gene related to congenital myasthenic syndrome type 20J M Pardal-Fernández, M C Carrascosa-Romero, S Álvarez, et al.
Neuromuscular Disorders : NMD|June 27, 2017
Reliability and validity analyses of the North Star Ambulatory Assessment in Brazilian PortugueseLarissa O Okama, Lívia M Zampieri, Carina L Ramos, et al.
Neuromuscular Disorders : NMD|July 5, 2017
Exome sequencing identifies targets in the treatment-resistant ophthalmoplegic subphenotype of myasthenia gravisMelissa Nel, Mahjoubeh Jalali Sefid Dashti, Junaid Gamieldien, et al.
Neuromuscular Disorders : NMD|July 5, 2017
Long-term follow-up of motor function and muscle strength in the congenital and childhood forms of myotonic dystrophy type 1Anna-Karin Kroksmark, Marie-Louise Stridh, Anne-Berit Ekström
Neuromuscular Disorders : NMD|May 22, 2017
A 9-year follow-up study of the natural progression of upper limb performance in myotonic dystrophy type 1: A similar decline for phenotypes but not for genderKateri Raymond, Mélanie Levasseur, Jean Mathieu, et al.
Neuromuscular Disorders : NMD|July 2, 2017
Rare diagnosis of telethoninopathy (LGMD2G) in a Turkish patientElena Ikenberg, Ivan Karin, Birgit Ertl-Wagner, et al.
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