Zobrazeno 1 - 4
of 4
pro vyhledávání: '"G. J. van Ekeren"'
Publikováno v:
European Journal of Pediatrics. 152:255-259
The objectives of this study were to describe the course of two forms of an hereditary syndrome characterised by congenital cataract, mitochondrial myopathy of heart and skeletal muscle and lactic acidosis. We also sought to determine clinical, physi
Publikováno v:
International journal of experimental pathology. 73(1)
In order to test the hypothesis that subsarcolemmal aggregation of skeletal muscle mitochondria, as noted in some patients with mitochondrial myopathies, is caused by an impaired oxygen supply to mitochondria, we exposed two groups of rats to 8% O2 d
Publikováno v:
European journal of pediatrics. 150(10)
Muscle biopsies from 17 children with exercise intolerance and other miscellaneous symptoms and signs showed changes in mitochondrial content. The patients could not be classified according to known criteria. The histopathological changes were quanti
Autor:
G. J. M. Egberink, O. Daniels, K. Kubat, R. C. A. Sengers, Ad M. Stadhouders, G. J. van Ekeren
Publikováno v:
Virchows Archiv A Pathological Anatomy and Histopathology. 412:47-52
A six day old boy died from an hereditary hypertrophic cardiomyopathy which was associated with mitochondrial myopathy of skeletal muscle, congenital cataract and lactic acidosis. In heart and skeletal muscle identical mitochondrial abnormalities wer