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	21.	Isolated cytochrome c oxidase deficiency as a cause of MELAS. [electronic resource] by Rossmanith, W Freilinger, M Roka, J Raffelsberger, T Moser-Thier, K Prayer, D Bernert, G Bittner, R E Producer: 20080312 In: Journal of medical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	MAP1B is required for axon guidance and Is involved in the development of the central and peripheral nervous system. [electronic resource] by Meixner, A Haverkamp, S Wässle, H Führer, S Thalhammer, J Kropf, N Bittner, R E Lassmann, H Wiche, G Propst, F Producer: 20010117 In: The Journal of cell biology vol. 151 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Sarcolemmal expression of dystrophin C-terminus but reduced expression of 6q-dystrophin-related protein in two DMD patients with large deletions of the dystrophin gene. [electronic resource] by Bittner, R E Shorny, S Ferlings, R Sperl, W Kress, W Müller, C R Cremer, M Léger, J J Voit, T Producer: 19950706 In: Neuromuscular disorders : NMD vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Effects of oral creatine supplementation in a patient with MELAS phenotype and associated nephropathy. [electronic resource] by Barisic, N Bernert, G Ipsiroglu, O Stromberger, C Müller, T Gruber, S Prayer, D Moser, E Bittner, R E Stöckler-Ipsiroglu, S Producer: 20021016 In: Neuropediatrics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Recruitment of bone-marrow-derived cells by skeletal and cardiac muscle in adult dystrophic mdx mice. [electronic resource] by Bittner, R E Schöfer, C Weipoltshammer, K Ivanova, S Streubel, B Hauser, E Freilinger, M Höger, H Elbe-Bürger, A Wachtler, F Producer: 19990618 In: Anatomy and embryology vol. 199 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene. [electronic resource] by Haubenberger, D Bittner, R E Rauch-Shorny, S Zimprich, F Mannhalter, C Wagner, L Mineva, I Vass, K Auff, E Zimprich, A Producer: 20060414 In: Neurology vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation. [electronic resource] by Vafiadaki, E Reis, A Keers, S Harrison, R Anderson, L V Raffelsberger, T Ivanova, S Hoger, H Bittner, R E Bushby, K Bashir, R Producer: 20010607 In: Neuroreport vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Two novel mutations in the GDAP1 and PRX genes in early onset Charcot-Marie-Tooth syndrome. [electronic resource] by Auer-Grumbach, M Fischer, C Papić, L John, E Plecko, B Bittner, R E Bernert, G Pieber, T R Miltenberger, G Schwarz, R Windpassinger, C Grill, F Timmerman, V Speicher, M R Janecke, A R Producer: 20080731 In: Neuropediatrics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B. [electronic resource] by Bittner, R E Anderson, L V Burkhardt, E Bashir, R Vafiadaki, E Ivanova, S Raffelsberger, T Maerk, I Höger, H Jung, M Karbasiyan, M Storch, M Lassmann, H Moss, J A Davison, K Harrison, R Bushby, K M Reis, A Producer: 19991019 In: Nature genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Pompe disease in Austria: clinical, genetic and epidemiological aspects. [electronic resource] by Löscher, W N Huemer, M Stulnig, T M Simschitz, P Iglseder, S Eggers, C Moser, H Möslinger, D Freilinger, M Lagler, F Grinzinger, S Reichhardt, M Bittner, R E Schmidt, W M Lex, U Brunner-Krainz, M Quasthoff, S Wanschitz, J V Producer: 20180727 In: Journal of neurology vol. 265 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)