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	1.	Apoptosis and ROS detoxification enzymes correlate with cytochrome c oxidase deficiency in mitochondrial encephalomyopathies. [electronic resource] by Di Giovanni, S Mirabella, M Papacci, M Odoardi, F Silvestri, G Servidei, S Producer: 20010712 In: Molecular and cellular neurosciences vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Peripheral neuropathy with giant axons and cardiomyopathy associated with desmin type intermediate filaments in skeletal muscle. [electronic resource] by Sabatelli, M Bertini, E Ricci, E Salviati, G Magi, S Papacci, M Tonali, P Producer: 19921006 In: Journal of the neurological sciences vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Reducing body myopathy and desmin storage in skeletal muscle: morphological and biochemical findings. [electronic resource] by Bertini, E Salviati, G Apollo, F Ricci, E Servidei, S Broccolini, A Papacci, M Tonali, P Producer: 19940422 In: Acta neuropathologica vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Single-fiber PCR in MELAS(3243) patients: correlations between intratissue distribution and phenotypic expression of the mtDNA(A3243G) genotype. [electronic resource] by Silvestri, G Rana, M Odoardi, F Modoni, A Paris, E Papacci, M Tonali, P Servidei, S Producer: 20001026 In: American journal of medical genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a family. [electronic resource] by Manfredi, G Silvestri, G Servidei, S Ricci, E Mirabella, M Bertini, E Papacci, M Rana, M Tonali, P Producer: 19930511 In: Journal of the neurological sciences vol. 115 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia. [electronic resource] by Luigetti, M Modoni, A Renna, R Silvestri, G Ricci, E Montano, N Tasca, G Papacci, M Monforte, M Conte, A Pomponi, M G Sabatelli, M Producer: 20110208 In: Clinical neurology and neurosurgery vol. 112 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)