Diagnostischer Stellenwert eines kranialen MRT bei kongenitaler Muskeldystrophie
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Radiology, Nuclear Medicine and imaging
Link
http://link.springer.com/content/pdf/10.1007/BF03043442.pdf
Reference15 articles.
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2. Dubowitz V. Muscle disorders in childhood, 2nd edn. London-Philadelphia-Toronto-Sydney-Tokyo: Saunders, 1995: 34–133.
3. Herrmann R, Straub V, Meyer K, et al. Congenital muscular dystrophy with laminin α2-chain deficiency: Identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry. Eur J Pediatr 1996;155:968–76.
4. Mercuri E, Muntoni F, Berardinelli A, et al. Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status. Neuropediatrics 1995;26:3–7.
5. Mercuri E, Pennock J, Goodwin F, et al. Sequential study of central and peripheral nervous system involvement in an infant with merosin deficient congenital muscular dystrophy. Neuromusc Disord 1996;6:425–9.
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