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	461.	Inclusion body myositis functional rating scale: a reliable and valid measure of disease severity. [electronic resource] by Jackson, C E Barohn, R J Gronseth, G Pandya, S Herbelin, L Producer: 20080522 In: Muscle & nerve vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	462.	Autoantibodies against a 43 KDa muscle protein in inclusion body myositis. [electronic resource] by Salajegheh, Mohammad Lam, Theresa Greenberg, Steven A Producer: 20110923 In: PloS one vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	463.	Novel GNE mutations in autosomal recessive hereditary inclusion body myopathy patients. [electronic resource] by No, Daniel Valles-Ayoub, Yadira Carbajo, Rosangela Khokher, Zeshan Sandoval, Lucia Stein, Beth Tarnopolsky, Mark Andrew Mozaffar, Tahseen Darvish, Babak Pietruszka, Marvin Darvish, Daniel Producer: 20131030 In: Genetic testing and molecular biomarkers vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	464.	Intramuscular dissociation of echogenicity in the triceps surae characterizes sporadic inclusion body myositis. [electronic resource] by Nodera, H Takamatsu, N Matsui, N Mori, A Terasawa, Y Shimatani, Y Osaki, Y Maruyama, K Izumi, Y Kaji, R Producer: 20161213 In: European journal of neurology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	465.	Muscular dystrophy in adult and aged anti-NGF transgenic mice resembles an inclusion body myopathy. [electronic resource] by Capsoni, S Ruberti, F Di Daniel, E Cattaneo, A Producer: 20000428 In: Journal of neuroscience research vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	466.	Congenital myopathy with tubular aggregates and tubulofilamentous IBM-type inclusions. [electronic resource] by Fidziańska, A Kamińska, A Ryniewicz, B Producer: 20050520 In: Neuropediatrics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	467.	ANT1 is reduced in sporadic inclusion body myositis. [electronic resource] by Barca, E Aguennouz, M Mazzeo, A Messina, S Toscano, A Vita, G L Portaro, S Parisi, D Rodolico, C Producer: 20130723 In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	468.	Novel GNE mutations in two phenotypically distinct HIBM2 patients. [electronic resource] by Weihl, Conrad C Miller, Sara E Zaidman, Craig M Pestronk, Alan Baloh, Robert H Al-Lozi, Mohammed Producer: 20110421 In: Neuromuscular disorders : NMD vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	469.	A Brazilian family with inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia linked to the VCP pGly97Glu mutation. [electronic resource] by Shinjo, Samuel Katsuyuki Oba-Shinjo, Sueli Mieko Lerario, Antonio Marcondes Marie, Suely Kazue Nagahashi Producer: 20180907 In: Clinical rheumatology vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	470.	119th ENMC international workshop: trial design in adult idiopathic inflammatory myopathies, with the exception of inclusion body myositis, 10-12 October 2003, Naarden, The Netherlands. [electronic resource] by Hoogendijk, Jessica E Amato, Anthony A Lecky, Bryan R Choy, Ernest H Lundberg, Ingrid E Rose, Michael R Vencovsky, Jiri de Visser, Marianne Hughes, Richard A Producer: 20040621 In: Neuromuscular disorders : NMD vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	471.	Hereditary inclusion body myopathy with a novel mutation in the GNE gene associated with proximal leg weakness and necrotizing myopathy. [electronic resource] by Motozaki, Y Komai, K Hirohata, M Asaka, T Ono, K Yamada, M Producer: 20070926 In: European journal of neurology vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	472.	Synaptic dysfunction does not contribute to muscle weakness in inclusion-body myositis. [electronic resource] by Badrising, Umesh A Verschuuren, Jan J G M Wintzen, Axel R van Dijk, J Gert Producer: 20070327 In: Muscle & nerve vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	473.	[Inclusion body myositis (IBM) -- a review]. [electronic resource] by Czaplinski, A Renaud, S Fuhr, P Producer: 20030609 In: Praxis vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	474.	Intravenous immunoglobulin for dysphagia of inclusion body myositis. [electronic resource] by Cherin, P Pelletier, S Teixeira, A Laforet, P Simon, A Herson, S Eymard, B Producer: 20020402 In: Neurology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	475.	[Immunocytochemical analysis of the inflammatory infiltrate in inclusion body myositis and other neuromuscular disorders with rimmed vacuoles]. [electronic resource] by Scola, R H Werneck, L C Iwamoto, F M de Messias, I T Tsuchiya, L V Producer: 19981223 In: Arquivos de neuro-psiquiatria vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	476.	[The practice guideline 'Dermatomyositis, polymyositis and sporadic inclusion body myositis']. [electronic resource] by Hoogendijk, J E Bijlsma, J W J van Engelen, B G M Lindeman, E van Royen-Kerkhof, A de Rie, M A de Visser, M Jennekens, F G I Producer: 20051104 In: Nederlands tijdschrift voor geneeskunde vol. 149 Availability: No items available. Save to lists Add to cart (remove)
	477.	The spectrum of GNE mutations: allelic heterogeneity for a common phenotype. [electronic resource] by Grandis, Marina Gulli, Rossella Cassandrini, Denise Gazzerro, Elisabetta Benedetti, Luana Narciso, Eleonora Nobbio, Lucilla Bruno, Claudio Minetti, Carlo Bellone, Emilia Reni, Lizia Mancardi, Giovanni Luigi Mandich, Paola Schenone, Angelo Producer: 20100818 In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	478.	Aluminum inclusion macrophagic myofasciitis: a recently identified condition. [electronic resource] by Gherardi, Romain K Authier, François-Jérôme Producer: 20040218 In: Immunology and allergy clinics of North America vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	479.	Molecular mechanisms of α-crystallinopathy and its therapeutic strategy. [electronic resource] by Sanbe, Atsushi Producer: 20120426 In: Biological & pharmaceutical bulletin vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	480.	Inclusion body myositis in Alzheimer's disease. [electronic resource] by Roos, P M Vesterberg, O Nordberg, M Producer: 20120529 In: Acta neurologica Scandinavica vol. 124 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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