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Molecular Genetics and Metabolism|December 26, 2001
A novel nonsense mutation (R269X) in the myophosphorylase gene in a patient with McArdle diseaseM Deschauer, J R Opalka, A Lindner, et al.Neuromuscular Disorders : NMD|March 1, 1996
An autosomal-recessive congenital myasthenic syndrome with tubular aggregates in a Libyan familyJ P Sieb, K Tolksdorf, R Dengler, et al.Fortschritte Der Neurologie-Psychiatrie|January 15, 2008
[Neuromyelitis optica: a separate disease entity associated with aquaporin-4-antibodies]B Jordan, K Eger, M E Kornhuber, et al.Deutsche Medizinische Wochenschrift (1946)|March 2, 1990
[Abnormal regulation of carnitine palmitoyltransferase in monozygotic twins as the cause of rhabdomyolysis]J P Schröder, W Mau, S Schumacher, et al.Muscle & Nerve|January 20, 2000
Relation between maximum discharge rates on electromyography and motor unit number estimatesW J Schulte-Mattler, D Georgiadis, K Tietze, et al.Muscle & Nerve|April 1, 1996
Muscle fatigue, lactate, and pyruvate in mitochondrial myopathy with progressive external ophthalmoplegiaR Dengler, K Wohlfarth, S Zierz, et al.Neurological Research|November 25, 2000
Automated identification of Doppler microembolic signals: comparison of two techniquesD Georgiadis, F Uhlmann, M Astler, et al.Neuromuscular Disorders : NMD|April 19, 2005
Dilated cardiomyopathy may be an early sign of the C826A Fukutin-related protein mutationT Müller, M Krasnianski, R Witthaut, et al.The Clinical Investigator|May 1, 1994
Myotonic dystrophy and limb girdle muscular dystrophy in one familyR Schröder, S Beyenburg, J Weber, et al.Journal of Neurology|January 28, 2021
Physical fatigability and muscle pain in patients with Hashimoto thyroiditisB Jordan, O Uer, T Buchholz, et al.Pageof 19