A Modoni, A D'Amico, B Dallapiccola… - Journal of Clinical …, 2011 - journals.lww.com From the *Department of Neuroscience, Catholic University; †Bambino Gesù Research Pediatric Hospital; ‡IRCCS CSS-Mendel Institute; §Department of Experimental Medicine, Sapienza University, Rome, Italy; ∥Muscle Unit, Medical Genetics Section, Department of ... Related articles - All 4 versions
RJ Barohn, YX Wang, LL Herbelin, B Bundy… - 2011 - discovery.ucl.ac.uk ... Phase II Therapeutic Trial of Mexiletine in Non-Dystrophic Myotonia. ... Full text not available from this repository. Type: Proceedings paper. Title: Phase II Therapeutic Trial of Mexiletine in Non-Dystrophic Myotonia. Event: 63rd AAN Annual Meeting. Location: Honolulu, HI. ... Cached
P Hilbert, S Frank, O Raheem… - Acta Neurologica …, 2011 - Wiley Online Library ... Letter to the Editor. Normal muscle MRI does not preclude increased connective tissue in muscle of recessive myotonia congenita. P. Hilbert 1,2 ,; S. Frank 3 ,; O. Raheem 4 ,; T. Suominen 4 ,; S. Penttilä 4 ,; B. Udd 4 ,; D. Fischer 1,2. Article first published online: 7 JUL 2011. ... All 2 versions
JM Statland, Y Wang, R Richesson… - Muscle & …, 2011 - Wiley Online Library Although many promising drugs have been evaluated for the treatment of myotonia, there are no US Food and Drug Administration (FDA)-approved treatments for NDM.11 In a Cochrane Collaboration review looking at treatment in myotonic disorders, one of the major ... Related articles - All 2 versions
V Bissay, K Keymolen, W Lissens… - Journal of the …, 2011 - Elsevier Skeletal muscle sodium channelopathies are rare autosomal inherited diseases, resulting from missense mutations in the SCN4A-gene, encoding for the alpha-subunit of the skeletal muscle sodium channels. To date, recognised phenotypes are paramyotonia congenita, ...
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