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	21.	Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations. [electronic resource] by Tulinius, M H Holme, E Kristiansson, B Larsson, N G Oldfors, A Producer: 19910904 In: The Journal of pediatrics vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Mitochondrial myopathy and cardiomyopathy in siblings. [electronic resource] by Tulinius, M H Eriksson, B O Hjalmarson, O Holme, E Oldfors, A Producer: 19890817 In: Pediatric neurology vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Neuropathology in Kearns-Sayre syndrome. [electronic resource] by Oldfors, A Fyhr, I M Holme, E Larsson, N G Tulinius, M Producer: 19910117 In: Acta neuropathologica vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres. [electronic resource] by Oldfors, A Larsson, N G Holme, E Tulinius, M Kadenbach, B Droste, M Producer: 19920923 In: Journal of the neurological sciences vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Cardiomyopathy in children with mitochondrial disease; clinical course and cardiological findings. [electronic resource] by Holmgren, D Wåhlander, H Eriksson, B O Oldfors, A Holme, E Tulinius, M Producer: 20030320 In: European heart journal vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Mitochondrial encephalomyopathy. A variant with heart failure and liver steatosis. [electronic resource] by Oldfors, A Tulinius, M Holme, E Kalimo, H Kristiansson, B Eriksson, B O Producer: 19871209 In: Acta neuropathologica vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Multiple symmetric lipomas with high levels of mtDNA with the tRNA(Lys) A-->G(8344) mutation as the only manifestation of disease in a carrier of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome. [electronic resource] by Holme, E Larsson, N G Oldfors, A Tulinius, M Sahlin, P Stenman, G Producer: 19930408 In: American journal of human genetics vol. 52 Availability: No items available. Save to lists Add to cart (remove)
	28.	SURF1 gene mutations in three cases with Leigh syndrome and cytochrome c oxidase deficiency. [electronic resource] by Moslemi, A-R Tulinius, M Darin, N Aman, P Holme, E Oldfors, A Producer: 20040319 In: Neurology vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy. [electronic resource] by Houshmand, M Larsson, N G Holme, E Oldfors, A Tulinius, M H Andersen, O Producer: 19940513 In: Biochimica et biophysica acta vol. 1226 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Progressive encephalopathy and complex I deficiency associated with mutations in MTND1. [electronic resource] by Moslemi, A-R Darin, N Tulinius, M Wiklund, L-M Holme, E Oldfors, A Producer: 20080731 In: Neuropediatrics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Whole body vibration therapy in patients with Duchenne muscular dystrophy--a prospective observational study. [electronic resource] by Söderpalm, A-C Kroksmark, A-K Magnusson, P Karlsson, J Tulinius, M Swolin-Eide, D Producer: 20131203 In: Journal of musculoskeletal & neuronal interactions vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	32.	Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her child. [electronic resource] by Larsson, N G Eiken, H G Boman, H Holme, E Oldfors, A Tulinius, M H Producer: 19920304 In: American journal of human genetics vol. 50 Availability: No items available. Save to lists Add to cart (remove)
	33.	Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiency. [electronic resource] by Darin, N Moslemi, A-R Lebon, S Rustin, P Holme, E Oldfors, A Tulinius, M Producer: 20040415 In: Neuropediatrics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	Inflammation and response to steroid treatment in limb-girdle muscular dystrophy 2I. [electronic resource] by Darin, N Kroksmark, A-K Ahlander, A-C Moslemi, A-R Oldfors, A Tulinius, M Producer: 20080214 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	Leigh syndrome with cytochrome-c oxidase deficiency and a single T insertion nt 5537 in the mitochondrial tRNATrp gene. [electronic resource] by Tulinius, M Moslemi, A-R Darin, N Westerberg, B Wiklund, L-M Holme, E Oldfors, A Producer: 20030709 In: Neuropediatrics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome. [electronic resource] by Larsson, N G Tulinius, M H Holme, E Oldfors, A Andersen, O Wahlström, J Aasly, J Producer: 19930114 In: American journal of human genetics vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	37.	De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspring. [electronic resource] by Tulinius, M H Houshmand, M Larsson, N G Holme, E Oldfors, A Holmberg, E Wahlström, J Producer: 19950928 In: Human genetics vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Bone markers and bone mineral density in Duchenne muscular dystrophy. [electronic resource] by Söderpalm, A C Magnusson, P Ahlander, A C Karlsson, J Kroksmark, A K Tulinius, M Swolin-Eide, D Producer: 20081204 In: Journal of musculoskeletal & neuronal interactions vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	39.	Atypical presentation of multisystem disorders in two girls with mitochondrial DNA deletions. [electronic resource] by Tulinius, M H Oldfors, A Holme, E Larsson, N G Houshmand, M Fahleson, P Sigström, L Kristiansson, B Producer: 19950427 In: European journal of pediatrics vol. 154 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	Mitochondrial myopathy with exercise intolerance and retinal dystrophy in a sporadic patient with a G583A mutation in the mt tRNA(phe) gene. [electronic resource] by Darin, N Kollberg, G Moslemi, A-R Tulinius, M Holme, E Grönlund, M Andersson Andersson, S Oldfors, A Producer: 20061120 In: Neuromuscular disorders : NMD vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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