Therapeutics in Duchenne muscular dystrophy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical)
Link
http://www.springerlink.com/index/pdf/10.1016/j.nurx.2006.01.005
Reference97 articles.
1. Beenakker EA, Maurits NM, Fock JM, Brouwer OF, van der Hoeven JH. Functional ability and muscle force in healthy children and ambulant Duchenne muscular dystrophy patients.Eur J Paediatr Neurol 2005.
2. Kroksmark AK, Beckung E, Tulinius M. Muscle strength and motor function in children and adolescents with spinal muscular atrophy II and III.Eur J Paediatr Neurol 5: 191–198, 2001.
3. Merlini L, Bertini E, Minetti C, Mongini T, Morandi L, Angelini C, et al. Motor function-muscle strength relationship in spinal muscular atrophy.Muscle Nerve 29: 548–552, 2004.
4. Escolar DM, Buyse G, Henricson E, Leshner R, Florence J, Mayhew J, et al. CINRG randomized controlled trial of creatine and glutamine in Duchenne muscular dystrophy.Ann Neurol 58: 151–155, 2005.
5. Brooke MH, Fenichel GM, Griggs RC, Mendell JR, Moxley R, Florence J, et al. Duchenne muscular dystrophy: patterns of clinical progression and effects of supportive therapy.Neurology 39: 475–481, 1989.
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