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	1.	[Current status of mitochondrial diseases]. [electronic resource] by Lombès, A Producer: 19981030 In: Revue neurologique vol. 154 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Diagnostic investigations of mitochondrial diseases with neurological symptoms]. [electronic resource] by Auré, K Lombès, A Producer: 20070504 In: Revue neurologique vol. 163 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mitochondrial encephalomyopathies. [electronic resource] by Lombes, A Bonilla, E Dimauro, S Producer: 19891219 In: Revue neurologique vol. 145 Availability: No items available. Save to lists Add to cart (remove)
	4.	[Organization and dynamics of the mitochondrial compartment]. [electronic resource] by Malka, F Lombes, A Rojo, M Producer: 20040722 In: Morphologie : bulletin de l'Association des anatomistes vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	[Secondary mitochondrial cytopathy in childhood: a recent concept?]. [electronic resource] by Odièvre, M H Lombès, A Odièvre, M Producer: 20031028 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Analysis of the tissue distribution and inheritance of heteroplasmic mitochondrial DNA point mutation by denaturing gradient gel electrophoresis in MERRF syndrome. [electronic resource] by Lombès, A Diaz, C Romero, N B Ziegler, F Fardeau, M Producer: 19930527 In: Neuromuscular disorders : NMD vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	[Research methods in metabolic myopathies in children]. [electronic resource] by Lombes, A Ogier, H Bonnefont, J P Munnich, A Saudubray, J M Producer: 19880310 In: Annales de medecine interne vol. 138 Availability: No items available. Save to lists Add to cart (remove)
	8.	Task force guidelines handbook: EFNS guidelines on diagnosis and management of fatty acid mitochondrial disorders. [electronic resource] by Angelini, C Federico, A Reichmann, H Lombes, A Chinnery, P Turnbull, D Producer: 20060911 In: European journal of neurology vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Myoblast xenotransplantation as a tool to evaluate the appropriateness of nanoparticular versus cellular trackers. [electronic resource] by Praud, C Vauchez, K Lombes, A Fiszman, M Y Vilquin, J T Producer: 20090504 In: Cell transplantation vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Modulation of mitochondrial morphology by bioenergetics defects in primary human fibroblasts. [electronic resource] by Guillery, O Malka, F Frachon, P Milea, D Rojo, M Lombès, A Producer: 20080813 In: Neuromuscular disorders : NMD vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Mitochondrial encephalomyopathies. [electronic resource] by DiMauro, S Bonilla, E Lombes, A Shanske, S Minetti, C Moraes, C T Producer: 19901119 In: Neurologic clinics vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	12.	A new case of methylmalonic aciduria with unexplained negative urinary methylmalonic colorimetric test. [electronic resource] by Charpentier, C Coude, M Perignon, J L Lombes, A Saudubray, J M Divry, P Producer: 19870427 In: Journal of inherited metabolic disease vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	In vivo functional investigations of lactic acid in patients with respiratory chain disorders. [electronic resource] by Touati, G Rigal, O Lombès, A Frachon, P Giraud, M Ogier de Baulny, H Producer: 19970321 In: Archives of disease in childhood vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Exhaustive scanning approach to screen all the mitochondrial tRNA genes for mutations and its application to the investigation of 35 independent patients with mitochondrial disorders. [electronic resource] by Sternberg, D Danan, C Lombès, A Laforêt, P Girodon, E Goossens, M Amselem, S Producer: 19980226 In: Human molecular genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	[A case of mitochondrial cytopathy (MERFF) without ragged red fibers at the onset]. [electronic resource] by Gignoux, L Maisonobe, T Laforet, P Lombès, A Lyon-Caen, O Fontaine, B Producer: 20010823 In: Revue neurologique vol. 157 Availability: No items available. Save to lists Add to cart (remove)
	16.	Clinical and biochemical features of 10 adult patients with muscle phosphorylase kinase deficiency. [electronic resource] by Wilkinson, D A Tonin, P Shanske, S Lombes, A Carlson, G M DiMauro, S Producer: 19940429 In: Neurology vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Impact on oxidative phosphorylation of immortalization with the telomerase gene. [electronic resource] by Auré, K Mamchaoui, K Frachon, P Butler-Browne, G S Lombès, A Mouly, V Producer: 20070724 In: Neuromuscular disorders : NMD vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesis. [electronic resource] by Nakase, H Moraes, C T Rizzuto, R Lombes, A DiMauro, S Schon, E A Producer: 19900404 In: American journal of human genetics vol. 46 Availability: No items available. Save to lists Add to cart (remove)
	19.	A non-ischemic forearm exercise test for the screening of patients with exercise intolerance. [electronic resource] by Hogrel, J Y Laforêt, P Ben Yaou, R Chevrot, M Eymard, B Lombès, A Producer: 20010802 In: Neurology vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Functional mitochondrial heterogeneity in heteroplasmic cells carrying the mitochondrial DNA mutation associated with the MELAS syndrome (mitochondrial encephalopathy, lactic acidosis, and strokelike episodes). [electronic resource] by Bakker, A Barthélémy, C Frachon, P Chateau, D Sternberg, D Mazat, J P Lombès, A Producer: 20001120 In: Pediatric research vol. 48 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 83 results.