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	61.	Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy and deafness (DIDMOAD, Wolfram syndrome). [electronic resource] by Rötig, A Cormier, V Chatelain, P Francois, R Saudubray, J M Rustin, P Munnich, A Producer: 19950817 In: Journal of inherited metabolic disease vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	[Metabolic and genetic investigations in childhood cardiomyopathies]. [electronic resource] by Bonnet, D Rustin, P Rötig, A de Lonlay, P Viot, G Munnich, A Sidi, D Producer: 20000118 In: Archives des maladies du coeur et des vaisseaux vol. 92 Availability: No items available. Save to lists Add to cart (remove)
	63.	Duplications of mitochondrial DNA in Kearns-Sayre syndrome. [electronic resource] by Poulton, J Morten, K J Marchington, D Weber, K Brown, G K Rötig, A Bindoff, L Producer: 19950808 In: Muscle & nerve. Supplement vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	Biochemical parameters for the diagnosis of mitochondrial respiratory chain deficiency in humans, and their lack of age-related changes. [electronic resource] by Chretien, D Gallego, J Barrientos, A Casademont, J Cardellach, F Munnich, A Rötig, A Rustin, P Producer: 19980220 In: The Biochemical journal vol. 329 ( Pt 2) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	Mitochondrial DNA deletion in Pearson's marrow/pancreas syndrome. [electronic resource] by Rotig, A Colonna, M Bonnefont, J P Blanche, S Fischer, A Saudubray, J M Munnich, A Producer: 19890524 In: Lancet (London, England) vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	Effect of idebenone on cardiomyopathy in Friedreich's ataxia: a preliminary study. [electronic resource] by Rustin, P von Kleist-Retzow, J C Chantrel-Groussard, K Sidi, D Munnich, A Rötig, A Producer: 19990902 In: Lancet (London, England) vol. 354 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	67.	Fluxes of nicotinamide adenine dinucleotides through mitochondrial membranes in human cultured cells. [electronic resource] by Rustin, P Parfait, B Chretien, D Bourgeron, T Djouadi, F Bastin, J Rötig, A Munnich, A Producer: 19960813 In: The Journal of biological chemistry vol. 271 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	Heart transplantation in children with mitochondrial cardiomyopathy. [electronic resource] by Bonnet, D Rustin, P Rötig, A Le Bidois, J Munnich, A Vouhé, P Kachaner, J Sidi, D Producer: 20011210 In: Heart (British Cardiac Society) vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	69.	The consequences of a mild respiratory chain deficiency on substrate competitive oxidation in human mitochondria. [electronic resource] by Geromel, V Parfait, B von Kleist-Retzow, J C Chretien, D Munnich, A Rötig, A Rustin, P Producer: 19970915 In: Biochemical and biophysical research communications vol. 236 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	70.	The investigation of respiratory chain disorders in heart using endomyocardial biopsies. [electronic resource] by Rustin, P Lebidois, J Chretien, D Bourgeron, T Piechaud, J F Rötig, A Sidi, D Munnich, A Producer: 19950817 In: Journal of inherited metabolic disease vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	71.	Superoxide-induced massive apoptosis in cultured skin fibroblasts harboring the neurogenic ataxia retinitis pigmentosa (NARP) mutation in the ATPase-6 gene of the mitochondrial DNA. [electronic resource] by Geromel, V Kadhom, N Cebalos-Picot, I Ouari, O Polidori, A Munnich, A Rötig, A Rustin, P Producer: 20010816 In: Human molecular genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	72.	Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathies. [electronic resource] by Rustin, P Lebidois, J Chretien, D Bourgeron, T Piechaud, J F Rötig, A Munnich, A Sidi, D Producer: 19940309 In: The Journal of pediatrics vol. 124 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	73.	Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia. [electronic resource] by Rötig, A de Lonlay, P Chretien, D Foury, F Koenig, M Sidi, D Munnich, A Rustin, P Producer: 19971114 In: Nature genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	74.	Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency. [electronic resource] by Bourgeron, T Rustin, P Chretien, D Birch-Machin, M Bourgeois, M Viegas-Péquignot, E Munnich, A Rötig, A Producer: 19951102 In: Nature genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	75.	Pearson syndrome: altered tricarboxylic acid and urea-cycle metabolites, adrenal insufficiency and corneal opacities. [electronic resource] by Ribes, A Riudor, E Valcárel, R Salvá, A Castelló, F Murillo, S Dominguez, C Rötig, A Jakobs, C Producer: 19950817 In: Journal of inherited metabolic disease vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	76.	Macular dystrophy, diabetes, and deafness associated with a large mitochondrial DNA deletion. [electronic resource] by Souied, E H Salès, M J Soubrane, G Coscas, G Bigorie, B Kaplan, J Munnich, A Rötig, A Producer: 19980129 In: American journal of ophthalmology vol. 125 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	77.	A case of Pearson syndrome associated with multiple renal cysts. [electronic resource] by Gürgey, A Ozalp, I Rötig, A Coşkun, T Tekinalp, G Erdem, G Akeören, Z Caglar, M Bakkaloglu, A Producer: 19970206 In: Pediatric nephrology (Berlin, Germany) vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	78.	Deletion of blood mitochondrial DNA in pancytopenia. [electronic resource] by Rötig, A Colonna, M Blanche, S Fischer, A Le Deist, F Frezal, J Saudubray, J M Munnich, A Producer: 19881005 In: Lancet (London, England) vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	79.	Clinical presentation of mitochondrial disorders in childhood. [electronic resource] by Munnich, A Rötig, A Chretien, D Cormier, V Bourgeron, T Bonnefont, J P Saudubray, J M Rustin, P 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)
	80.	Widespread multi-tissue deletions of the mitochondrial genome in the Pearson marrow-pancreas syndrome. [electronic resource] by Cormier, V Rötig, A Quartino, A R Forni, G L Cerone, R Maier, M Saudubray, J M Munnich, A Producer: 19901105 In: The Journal of pediatrics vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 143 results.