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Morphol Embryol (Bucur) ; 30(2): 123-8, 1984.
Article in English | MEDLINE | ID: mdl-6234457

ABSTRACT

The author's 15-year experience in the investigation of progressive muscular dystrophy (PMD) is presented. Clinical and paraclinical (biochemical, electromyographical and morphohistochemical) parameters were estimated and correlated in patients with facioscapulohumeral (FSH), Duchenne (D) and limb-girdle (LG) types of muscular dystrophy. The value of each kind of investigation was also estimated in the establishment of the anatomoclinical diagnosis of a degenerative muscular affection.


Subject(s)
Muscular Dystrophies/diagnosis , Adolescent , Adult , Biopsy , Child , Child, Preschool , Clinical Enzyme Tests , Creatine/urine , Electrolytes/blood , Electromyography , Female , Histocytochemistry , Humans , Male , Muscles/pathology , Muscular Dystrophies/pathology
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