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	121.	De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy. [electronic resource] by Durling, H J Reilich, P Müller-Höcker, J Mendel, B Pongratz, D Wallgren-Pettersson, C Gunning, P Lochmüller, H Laing, N G Producer: 20030519 In: Neuromuscular disorders : NMD vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	122.	A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy. [electronic resource] by Jaksch, M Hofmann, S Kleinle, S Liechti-Gallati, S Pongratz, D E Müller-Höcker, J Jedele, K B Meitinger, T Gerbitz, K D Producer: 19990204 In: Journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	123.	Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies. [electronic resource] by Jaksch, M Kleinle, S Scharfe, C Klopstock, T Pongratz, D Müller-Höcker, J Gerbitz, K D Liechti-Gallati, S Lochmuller, H Horvath, R Producer: 20020107 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	124.	Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) gene. [electronic resource] by Jaksch, M Klopstock, T Kurlemann, G Dörner, M Hofmann, S Kleinle, S Hegemann, S Weissert, M Müller-Höcker, J Pongratz, D Gerbitz, K D Producer: 19981106 In: Annals of neurology vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	125.	IG-therasorb immunoapheresis in orthotopic xenotransplantation of baboons with landrace pig hearts. [electronic resource] by Brenner, P Reichenspurner, H Schmoeckel, M Wimmer, C Rucker, A Eder, V Meiser, B Hinz, M Felbinger, T Müller-Höcker, J Hammer, C Reichart, B Producer: 20000301 In: Transplantation vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	126.	Congenital cataract, muscular hypotonia, developmental delay and sensorineural hearing loss associated with a defect in copper metabolism. [electronic resource] by Horváth, R Freisinger, P Rubio, R Merl, T Bax, R Mayr, J A Müller-Höcker, J Pongratz, D Moller, L B Horn, N Jaksch, M Producer: 20050915 In: Journal of inherited metabolic disease vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	127.	A tRNA(Ala) mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy. [electronic resource] by Horváth, R Lochmüller, H Scharfe, C Do, B H Oefner, P J Müller-Höcker, J Schoser, B G Pongratz, D Auer, D P Jaksch, M Producer: 20031106 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	128.	MesP1 drives vertebrate cardiovascular differentiation through Dkk-1-mediated blockade of Wnt-signalling. [electronic resource] by David, R Brenner, C Stieber, J Schwarz, F Brunner, S Vollmer, M Mentele, E Müller-Höcker, J Kitajima, S Lickert, H Rupp, R Franz, W-M Producer: 20080326 In: Nature cell biology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	129.	Coenzyme Q10 deficiency and isolated myopathy. [electronic resource] by Horvath, R Schneiderat, P Schoser, B G H Gempel, K Neuen-Jacob, E Plöger, H Müller-Höcker, J Pongratz, D E Naini, A DiMauro, S Lochmüller, H Producer: 20060314 In: Neurology vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	130.	Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene. [electronic resource] by Horváth, R Scharfe, C Hoeltzenbein, M Do, B H Schröder, C Warzok, R Vogelgesang, S Lochmüller, H Müller-Höcker, J Gerbitz, K D Oefner, P J Jaksch, M Producer: 20021119 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	131.	Missense mutations of ACTA1 cause dominant congenital myopathy with cores. [electronic resource] by Kaindl, A M Rüschendorf, F Krause, S Goebel, H-H Koehler, K Becker, C Pongratz, D Müller-Höcker, J Nürnberg, P Stoltenburg-Didinger, G Lochmüller, H Huebner, A Producer: 20050414 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)
	132.	Prevention of hyperacute rejection by human decay accelerating factor in xenogeneic perfused working hearts. [electronic resource] by Schmoeckel, M Nollert, G Shahmohammadi, M Young, V K Chavez, G Kasper-König, W White, D J Müller-Höcker, J Arendt, R M Wilbert-Lampen, U Hammer, C Reichart, B Producer: 19961210 In: Transplantation vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	133.	Technique of immunoapheresis in heterotopic and orthotopic xenotransplantation of pig hearts into cynomolgus and rhesus monkeys. [electronic resource] by Brenner, P Schmoeckel, M Reichenspurner, H Felbinger, T Hinz, M Eder, V Rucker, A Wimmer, C Uchita, S Kriegeskorte, S Meiser, B Müller-Höcker, J Seidel, D Hammer, C Reichart, B Producer: 20000906 In: Transplantation proceedings vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	134.	Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts. [electronic resource] by Jaksch, M Paret, C Stucka, R Horn, N Müller-Höcker, J Horvath, R Trepesch, N Stecker, G Freisinger, P Thirion, C Müller, J Lunkwitz, R Rödel, G Shoubridge, E A Lochmüller, H Producer: 20020327 In: Human molecular genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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