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	21.	Yeast and human frataxin are processed to mature form in two sequential steps by the mitochondrial processing peptidase. [electronic resource] by Branda, S S Cavadini, P Adamec, J Kalousek, F Taroni, F Isaya, G Producer: 19990902 In: The Journal of biological chemistry vol. 274 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients. [electronic resource] by Taroni, F Verderio, E Dworzak, F Willems, P J Cavadini, P DiDonato, S Producer: 19930924 In: Nature genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	The Friedreich's ataxia mutation confers cellular sensitivity to oxidant stress which is rescued by chelators of iron and calcium and inhibitors of apoptosis. [electronic resource] by Wong, A Yang, J Cavadini, P Gellera, C Lonnerdal, B Taroni, F Cortopassi, G Producer: 19990503 In: Human molecular genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Clinical and molecular heterogeneity in very-long-chain acyl-coenzyme A dehydrogenase deficiency. [electronic resource] by Pons, R Cavadini, P Baratta, S Invernizzi, F Lamantea, E Garavaglia, B Taroni, F Producer: 20000511 In: Pediatric neurology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Assignment of the human carnitine palmitoyltransferase II gene (CPT1) to chromosome 1p32. [electronic resource] by Gellera, C Verderio, E Floridia, G Finocchiaro, G Montermini, L Cavadini, P Zuffardi, O Taroni, F Producer: 19950421 In: Genomics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations. [electronic resource] by Verderio, E Cavadini, P Montermini, L Wang, H Lamantea, E Finocchiaro, G DiDonato, S Gellera, C Taroni, F Producer: 19950516 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Molecular characterization of inherited carnitine palmitoyltransferase II deficiency. [electronic resource] by Taroni, F Verderio, E Fiorucci, S Cavadini, P Finocchiaro, G Uziel, G Lamantea, E Gellera, C DiDonato, S Producer: 19921022 In: Proceedings of the National Academy of Sciences of the United States of America vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Detection of the new emerging rabbit haemorrhagic disease type 2 virus (RHDV2) in Sicily from rabbit (Oryctolagus cuniculus) and Italian hare (Lepus corsicanus). [electronic resource] by Camarda, A Pugliese, N Cavadini, P Circella, E Capucci, L Caroli, A Legretto, M Mallia, E Lavazza, A Producer: 20151020 In: Research in veterinary science vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Molecular analysis of carnitine palmitoyltransferase II deficiency with hepatocardiomuscular expression. [electronic resource] by Bonnefont, J P Taroni, F Cavadini, P Cepanec, C Brivet, M Saudubray, J M Leroux, J P Demaugre, F Producer: 19960725 In: American journal of human genetics vol. 58 Availability: No items available. Save to lists Add to cart (remove)
	30.	Two CPT2 mutations in three Japanese patients with carnitine palmitoyltransferase II deficiency: functional analysis and association with polymorphic haplotypes and two clinical phenotypes. [electronic resource] by Wataya, K Akanuma, J Cavadini, P Aoki, Y Kure, S Invernizzi, F Yoshida, I Kira, J Taroni, F Matsubara, Y Narisawa, K Producer: 19980709 In: Human mutation vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Spillover Events of Infection of Brown Hares (Lepus europaeus) with Rabbit Haemorrhagic Disease Type 2 Virus (RHDV2) Caused Sporadic Cases of an European Brown Hare Syndrome-Like Disease in Italy and Spain. [electronic resource] by Velarde, R Cavadini, P Neimanis, A Cabezón, O Chiari, M Gaffuri, A Lavín, S Grilli, G Gavier-Widén, D Lavazza, A Capucci, L Producer: 20180509 In: Transboundary and emerging diseases vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)