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	81.	Site-specific deletions of the mitochondrial genome in the Pearson marrow-pancreas syndrome. [electronic resource] by Rötig, A Cormier, V Koll, F Mize, C E Saudubray, J M Veerman, A Pearson, H A Munnich, A Producer: 19910821 In: Genomics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	82.	A novel mutation in STXBP1 causing epileptic encephalopathy (late onset infantile spasms) with partial respiratory chain complex IV deficiency. [electronic resource] by Barcia, G Barnerias, C Rio, M Siquier-Pernet, K Desguerre, I Colleaux, L Munnich, A Rotig, A Nabbout, R Producer: 20140716 In: European journal of medical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	83.	Neonatal and delayed-onset liver involvement in disorders of oxidative phosphorylation. [electronic resource] by Cormier-Daire, V Chretien, D Rustin, P Rötig, A Dubuisson, C Jacquemin, E Hadchouel, M Bernard, O Munnich, A Producer: 19970610 In: The Journal of pediatrics vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	84.	A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiency. [electronic resource] by Valnot, I Kassis, J Chretien, D de Lonlay, P Parfait, B Munnich, A Kachaner, J Rustin, P Rötig, A Producer: 19990902 In: Human genetics vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	85.	Biochemical, genetic and immunoblot analyses of 17 patients with an isolated cytochrome c oxidase deficiency. [electronic resource] by von Kleist-Retzow, J C Vial, E Chantrel-Groussard, K Rötig, A Munnich, A Rustin, P Taanman, J W Producer: 19991022 In: Biochimica et biophysica acta vol. 1455 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	86.	Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritis. [electronic resource] by Rötig, A Goutières, F Niaudet, P Rustin, P Chretien, D Guest, G Mikol, J Gubler, M C Munnich, A Producer: 19950501 In: The Journal of pediatrics vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	87.	Renal failure from mitochondrial cytopathies. [electronic resource] by Buemi, M Allegra, A Rotig, A Gubler, M C Aloisi, C Corica, F Pettinato, G Frisina, N Niaudet, P Producer: 19970922 In: Nephron vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	88.	Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxia. [electronic resource] by Rötig, A Bessis, J L Romero, N Cormier, V Saudubray, J M Narcy, P Lenoir, G Rustin, P Munnich, A Producer: 19920304 In: American journal of human genetics vol. 50 Availability: No items available. Save to lists Add to cart (remove)
	89.	Hair and skin disorders as signs of mitochondrial disease. [electronic resource] by Bodemer, C Rötig, A Rustin, P Cormier, V Niaudet, P Saudubray, J M Rabier, D Munnich, A de Prost, Y Producer: 19990218 In: Pediatrics vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	90.	Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome. [electronic resource] by Bénit, P Slama, A Cartault, F Giurgea, I Chretien, D Lebon, S Marsac, C Munnich, A Rötig, A Rustin, P Producer: 20040224 In: Journal of medical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	91.	Carrier detection in a partially dominant X-linked disease: ornithine transcarbamylase deficiency. [electronic resource] by Pelet, A Rotig, A Bonaïti-Pellié, C Rabier, D Cormier, V Toumas, E Hentzen, D Saudubray, J M Munnich, A Producer: 19900227 In: Human genetics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	92.	Cytochrome c oxidase deficiency presenting as recurrent neonatal myoglobinuria. [electronic resource] by Saunier, P Chretien, D Wood, C Rötig, A Bonnefont, J P Saudubray, J M Rabier, D Munnich, A Rustin, P Producer: 19951127 In: Neuromuscular disorders : NMD vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	93.	The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway. [electronic resource] by Gimenez-Roqueplo, A P Favier, J Rustin, P Mourad, J J Plouin, P F Corvol, P Rötig, A Jeunemaitre, X Producer: 20020110 In: American journal of human genetics vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	94.	Liver cytochrome c oxidase deficiency in a case of neonatal-onset hepatic failure. [electronic resource] by Edery, P Gérard, B Chretien, D Rötig, A Cerrone, R Rabier, D Rambaud, C Fabre, M Saudubray, J M Munnich, A Producer: 19940613 In: European journal of pediatrics vol. 153 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	95.	Multiple deletions of mtDNA in two brothers with sideroblastic anemia and mitochondrial myopathy and in their asymptomatic mother. [electronic resource] by Casademont, J Barrientos, A Cardellach, F Rötig, A Grau, J M Montoya, J Beltrán, B Cervantes, F Rozman, C Estivill, X Producer: 19950404 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	96.	Variable outcome of growth hormone administration in respiratory chain deficiency. [electronic resource] by Romano, S Samara, D Crosnier, H Valayannopoulos, V Polak, M Chrétien, D Rötig, A Munnich, A Brauner, R de Lonlay, P Producer: 20080403 In: Molecular genetics and metabolism vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	97.	Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiency. [electronic resource] by Bourgeron, T Chretien, D Poggi-Bach, J Doonan, S Rabier, D Letouzé, P Munnich, A Rötig, A Landrieu, P Rustin, P Producer: 19940707 In: The Journal of clinical investigation vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	98.	Mitochondria transfection by oligonucleotides containing a signal peptide and vectorized by cationic liposomes. [electronic resource] by Geromel, V Cao, A Briane, D Vassy, J Rotig, A Rustin, P Coudert, R Rigaut, J P Munnich, A Taillandier, E Producer: 20020117 In: Antisense & nucleic acid drug development vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	99.	Inherited palmoplantar keratoderma and sensorineural deafness associated with A7445G point mutation in the mitochondrial genome. [electronic resource] by Martin, L Toutain, A Guillen, C Haftek, M Machet, M C Toledano, C Arbeille, B Lorette, G Rötig, A Vaillant, L Producer: 20001120 In: The British journal of dermatology vol. 143 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	100.	[Pearson's syndrome. Pancytopenia with exocrine pancreatic insufficiency: new mitochondrial disease in the first childhood]. [electronic resource] by Cormier, V Rötig, A Bonnefont, J P Mechinand, F Berthou, C Goulet, O Schmitz, J Blanche, S Vassaut, A Maier, M Producer: 19910718 In: Archives francaises de pediatrie vol. 48 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 143 results.