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Volumn 52, Issue 2, 2004, Pages 254-256

Congenital fiber type disproportion: A rare type of congenital myopathy: A report of four cases

Author keywords

Congenital fiber type disproportion; Congenital myopathy; Enzyme histochemistry; Muscle; Myopathic disorder

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CENTRONUCLEAR MYOPATHY; CHILD; CHILDHOOD DISEASE; CLINICAL FEATURE; CONGENITAL FIBER TYPE DISPROPORTION; CONTROLLED STUDY; DIAGNOSTIC PROCEDURE; DIFFERENTIAL DIAGNOSIS; FACE DYSMORPHIA; FEMALE; HISTOCHEMISTRY; HUMAN; HUMAN TISSUE; MALE; MOTOR DYSFUNCTION; MUSCLE BIOPSY; MUSCLE DISEASE; MUSCLE HYPOTONIA; MYOPATHY; BIOPSY; CYTOCHEMISTRY; METABOLISM; METHODOLOGY; PATHOLOGY; PRESCHOOL CHILD; SKELETAL MUSCLE; STAINING;

EID: 4344682618     PISSN: 00283886     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (5)

References (9)
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  • 3
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    • Congenital fibre type disproportion myopathy. A histological diagnosis with an uncertain clinical outlook
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  • 4
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    • Congenital myopathies
    • Mastalgia FL, (Ed). New York: Churchill Livingstone
    • Fardeau M. Congenital myopathies. In: Mastalgia FL, (Ed). Skeletal muscle pathology. New York: Churchill Livingstone 1992;237-8.
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  • 6
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  • 8
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    • Gayathri, N.1    Das, S.2    Vasanth, A.3    Devi, M.G.4    Ramamohan, Y.5    Santosh, Y.6
  • 9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.