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Volumn 40, Issue 12, 1998, Pages 807-811

Congenital muscular dystrophy with merosin deficiency: MRI findings in five patients

Author keywords

Congenital muscular dystrophy; Magnetic resonance imaging; Merosin

Indexed keywords

MEROSIN;

EID: 0031762583     PISSN: 00283940     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002340050689     Document Type: Article
Times cited : (32)

References (11)
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  • 2
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  • 3
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    • Vainzof M, Suely KNM, Reed UC, et al (1995) Deficiency of merosin (laminin M or α 2) in congenital muscular dystrophy associated with cerebral white matter alterations. Neuropediatrics 26: 293-297
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  • 4
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    • Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities
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    • Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse
    • Matsumura K, Yamada H, Saito F, et al (1997) Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse. Neuromusc Disord 7: 7-12
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  • 8
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    • Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping
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    • Congenital muscular dystrophy with laminin α2 chain deficiency: Identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry
    • Herrmann R, Straub V, Meyer K, et al (1996) 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 155: 968-976
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.