|
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;
ADOLESCENT;
BIOPSY;
CHILD;
CHILD, PRESCHOOL;
DIAGNOSIS, DIFFERENTIAL;
FEMALE;
HISTOCYTOCHEMISTRY;
HUMANS;
MALE;
MUSCLE, SKELETAL;
MYOPATHIES, STRUCTURAL, CONGENITAL;
STAINING AND LABELING;
|
EID: 4344682618
PISSN: 00283886
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (5)
|
References (9)
|