Your search returned 44 results.

Results
	41.	Borrelia burgdorferi myositis: report of eight patients. [electronic resource] by Reimers, C D de Koning, J Neubert, U Preac-Mursic, V Koster, J G Müller-Felber, W Pongratz, D E Duray, P H Producer: 19930811 In: Journal of neurology vol. 240 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	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)
	43.	The T102C polymorphism of the 5-HT2A-receptor gene in fibromyalgia. [electronic resource] by Bondy, B Spaeth, M Offenbaecher, M Glatzeder, K Stratz, T Schwarz, M de Jonge, S Krüger, M Engel, R R Färber, L Pongratz, D E Ackenheil, M Producer: 19991206 In: Neurobiology of disease vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	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)