Inherited Neuromuscular Disorders: Presentation, Diagnosis, and Advances in Treatment
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s40124-017-0118-7.pdf
Reference42 articles.
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2. Paro-panjan D, Neubauer D (2008) Congenital hypotonia: 439–442
3. Vasta I, Kinali M, Messina S, Guzzetta A, Kapellou O, Manzur A, Cowan F, Muntoni F, Mercuri E. Can clinical signs identify newborns with neuromuscular disorders? J Pediatr. 2005;146:73–9.
4. Prasad AN, Prasad C. Genetic evaluation of the floppy infant. Semin Fetal Neonatal Med. 2011;16:99–108.
5. Brockmann K, Becker P, Schreiber G, Neubert K, Brunner E, Bönnemann C. Sensitivity and specificity of qualitative muscle ultrasound in assessment of suspected neuromuscular disease in childhood. Neuromuscul Disord. 2007;17:517–23.
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