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	1.	Malignant hyperthermia and central core disease: analysis of two families with heterogeneous clinical expression. [electronic resource] by Romero, N B Nivoche, Y Lunardi, J Bruneau, B Cheval, M A Hillaire, D Fardeau, M Producer: 19940623 In: Neuromuscular disorders : NMD vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Immunohistochemical analysis of muscle cytochrome c oxidase deficiency in children. [electronic resource] by Possekel, S Lombes, A Ogier de Baulny, H Cheval, M A Fardeau, M Kadenbach, B Romero, N B Producer: 19950605 In: Histochemistry and cell biology vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation. [electronic resource] by Barthélémy, C Ogier de Baulny, H Diaz, J Cheval, M A Frachon, P Romero, N Goutieres, F Fardeau, M Lombès, A Producer: 20010614 In: Annals of neurology vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	4.	Clinical and molecular heterogeneity of cytochrome c oxidase deficiency in the newborn. [electronic resource] by Lombes, A Romero, N B Touati, G Frachon, P Cheval, M A Giraud, M Simon, D Ogier de Baulny, H Producer: 19961122 In: Journal of inherited metabolic disease vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Morphological studies of skeletal muscle in lactic acidosis. [electronic resource] by Romero, N B Lombès, A Touati, G Rigal, O Frachon, P Cheval, M A Giraud, M Possekel, S Fardeau, M Ogier de Baulny, H Producer: 19970130 In: Journal of inherited metabolic disease vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A point mutation in the glycerol kinase gene associated with a deletion in the dystrophin gene in a familial X-linked muscular dystrophy: non-contiguous gene syndrome involving Becker muscular dystrophy and glycerol kinase loci. [electronic resource] by Romero, N B Récan, D Rigal, O Leturcq, F Llense, S Barbot, J C Deburgrave, N Cheval, M A Deniau, F Kaplan, J C Producer: 19980310 In: Neuromuscular disorders : NMD vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)