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Biomedical subjects

C Calandi

Publications and source records attributed to C Calandi.

At least 19 recordsLinked to original sources
PubMed1984

[Blood myoglobin in children with progressive muscular dystrophy and in carriers].

We studied the behaviour of serum myoglobin in 32 children affected by Duchenne muscular dystrophy, in 30 mothers (10 definite carriers and 20 possible carriers), in 5 sisters (possible carriers) and in 40 healthy women (control). The serum myoglobin was always increased in the patients affected by Duchenne muscular dystrophy; the greatest values were in the patients who were still ambulant, with a behaviour similar to creatine kinase. In the carriers the myoglobinemia showed a significant increase in definite carriers, while there was no significant difference between the possible carriers and the controls.

Adolescent↗
PubMed1984

[Granulocyte function in Duchenne's progressive muscular dystrophy].

We studied the in vitro function of polymorphonuclear leukocytes in 14 patients affected by Duchenne muscular dystrophy, aged 2-14 years, especially the chemotaxis and the bactericidal activity. The chemotaxis appeared significantly reduced, while the bactericidal activity was sometimes reduced, sometimes increased. In this disease the polymorphonuclear leukocytes seems to have a reduced capacity of movement; probably this phenomenon is connected with an alteration of the muscular cellular apparatus, which perhaps is related with an electrolytic intercellular inequality. These findings are consistent with the definition of Duchenne muscular dystrophy as a systemic disease of the membrane with alterations not only of striped muscular fibers, but of various cells and tissues.

Adolescent↗
PubMed1980

[Structural and ultrastructural features of the skeletal muscle in Werdnig-Hoffmann disease].

In researches performed on striated muscles of individuals affected by various myopathies, fragments of gastrocnemius muscle in course of Werdnig-Hoffmann disease have been studied. The light microscopic observations demonstrate the presence of numerous, very thin, atrophic fibres with many irregularly lobated and packed nuclei alternating with apparently normal fibres with lighter and larger nuclei. The connective part of the muscle appears to be remarkably increased and replaces the atypical contractile tissue. The electron microscope shows, in the atrophic fibres, remarkable alterations of the sarcoplasmatic elements, and a complete disarrangement of myofibrils and myofilaments, some of which are anchored to fragments of the Z bands, irregularly arranged. Even the normal orientation of the sarcomeres often with indefinite bound, is upset. The numerous lobated nuclei totally occupy the irregular protrusions of the sarcoplasm, rich in peripheral microvesicles. In respect of other examined myopathies, in which the muscle fibres alterations affect limited parts of the contractile elements, in these cases the modifications seem to be of greater entity and to affect completely single muscle fibres.

Cytoskeleton↗
PubMed1979

[Further observations by electron microscope of striated muscle in progressive Duchenne muscular dystrophy].

Gastrocnemius muscle fragments of children affected by clinically diagnosed progressive muscular dystrophy of Duchenne have been studied. At the light microscope, in the semi-thin sections, the more evident changes are represented by a wide diameter range of the fibers and fatty infiltration. Some fibers show numerous nuclei in their central part, a sarcoplasmic degeneration of vacuolar type and an irregular and tortuous course of the myofibrils. Moreover, the ultrastructural findings have shown characteristic changes in myofilaments and Z bands represented by: streaming of the Z bands, collection of the triads and concentric laminated bodies. These observations have pointed out a certain gradualness of the alterations, starting from focal changes of Z band to the complete disarrangement of myofilaments.

Child↗