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Period of time: 2004年1期
Publisher: Elsevier
Founded in: 1991
Total resources: 4
ISSN: 0960-8966
Subject: R74 Neurology and Psychiatry
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Neuromuscular Disorders,volume 14,issue 1
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By Onengut S., Ugur S.A., Karasoy H., Yuceyar N., Tolun A. in (2004)
Neuromuscular Disorders,volume 14,issue 1 , Vol. 14, Iss. 1, 2004-01 , pp.![](/images/ico/ico5.png)
Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene
By Beroud C., Carrie A., Beldjord C., Deburgrave N., Llense S., Carelle N., Peccate C., Cuisset J.-M., Pandit F., Carre-Pigeon F., Mayer M., Bellance R., Recan D., Chelly J., Kaplan J.-C., Leturcq F. in (2004)
Neuromuscular Disorders,volume 14,issue 1 , Vol. 14, Iss. 1, 2004-01 , pp.![](/images/ico/ico5.png)
A-utrophin up-regulation in mdx skeletal muscle is independent of regeneration
By Weir A.P., Morgan J.E., Davies K.E. in (2004)
Neuromuscular Disorders,volume 14,issue 1 , Vol. 14, Iss. 1, 2004-01 , pp.![](/images/ico/ico5.png)
By Yasaki E., Prioleau C., Barbier J., Richard P., Andreux F., Leroy J.-P., Dartevelle P., Koenig J., Molgo J., Fardeau M., Eymard B., Hantai D. in (2004)
Neuromuscular Disorders,volume 14,issue 1 , Vol. 14, Iss. 1, 2004-01 , pp.![](/images/ico/ico5.png)
Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD)
By Tonini M.M.O., Passos-Bueno M.R., Cerqueira A., Matioli S.R., Pavanello R., Zatz M. in (2004)
Neuromuscular Disorders,volume 14,issue 1 , Vol. 14, Iss. 1, 2004-01 , pp.![](/images/ico/ico5.png)
Changes in motor cortex excitability in facioscapulohumeral muscular dystrophy
By Di Lazzaro V., Oliviero A., Tonali P.A., Felicetti L., De Marco M.B.P., Saturno E., Pilato F., Pescatori M., Dileone M., Pasqualetti P., Ricci E. in (2004)
Neuromuscular Disorders,volume 14,issue 1 , Vol. 14, Iss. 1, 2004-01 , pp.![](/images/ico/ico5.png)
A novel mutation in the mitochondrial tRNA Phe gene associated with mitochondrial myopathy
By Moslemi A.-R., Lindberg C., Toft J., Holme E., Kollberg G., Oldfors A. in (2004)
Neuromuscular Disorders,volume 14,issue 1 , Vol. 14, Iss. 1, 2004-01 , pp.![](/images/ico/ico5.png)
Muscle MRI in adult-onset acid maltase deficiency
By Pichiecchio A., Uggetti C., Ravaglia S., Egitto M.G., Rossi M., Sandrini G., Danesino C. in (2004)
Neuromuscular Disorders,volume 14,issue 1 , Vol. 14, Iss. 1, 2004-01 , pp.![](/images/ico/ico5.png)
By Wallgren-Pettersson C., Bushby K., Mellies U., Simonds A. in (2004)
Neuromuscular Disorders,volume 14,issue 1 , Vol. 14, Iss. 1, 2004-01 , pp.