@misc{Fidziańska-Dolot_Anna_(1930–2015)_Files_2010,
 author={Fidziańska-Dolot, Anna (1930–2015)},
 editor={Mossakowski Medical Research Center Polish Academy of Sciences. Department of Neuromuscular},
 copyright={Creative Commons Attribution BY 4.0 license},
 address={Warsaw},
 howpublished={online},
 year={2010},
 language={pol},
 abstract={A 50-year-old patient with suspected myopathy was examined. A biopsy of quadriceps sinister was performed. Electronmicroscopy analysis revealed unchanged myofibrils structure but quite numerous fat droplets were visible (Fig. 1,2). Mitochondrial ultrastructure was preserved, and sub-membranously located cell nuclei were seen (Fig. 3,4). Normal structure of the neuromuscular junction was observed but some mitochondria were characterized by partial lack of mitochondrial cristae (Fig. 5,6,7,8,9).Defect of mitochondrial enzymes was suspected. Biochemical examination of carnitine palmitoyltransferase in the muscle biopsy was performed and the result was 2,13 nM/mgB/min (norm 6,5-18 nM/mgB/min.).},
 title={Files for neuromuscular diseases (2010) - nr 29/10},
 type={Text},
 type={Image},
 URL={http://rcin.org.pl/Content/124271/PDF/29_10_calosc.pdf},
 keywords={Myopathy, Biceps quadriceps sinister},
}