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	1001.	[Multilocular Paget's disease in IBMPFD syndrome. A case report with 14-year follow-up]. [electronic resource] by Zajonz, D Langsieb, C Chavdarova, L Kellermann, S Baum, P Wickenhauser, C von Salis-Soglio, G Prietzel, T Producer: 20121107 In: Der Orthopade vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1002.	Expression of lysosome-related proteins and genes in the skeletal muscles of inclusion body myositis. [electronic resource] by Kumamoto, Toshihide Ueyama, Hidetsugu Tsumura, Hiroshi Toyoshima, Itaru Tsuda, Tomiyasu Producer: 20040503 In: Acta neuropathologica vol. 107 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1003.	A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family. [electronic resource] by Gu, Jie-Mei Ke, Yao-Hua Yue, Hua Liu, Yu-Juan Zhang, Zeng Zhang, Hao Hu, Wei-Wei Wang, Chun He, Jin-Wei Hu, Yun-Qiu Li, Miao Fu, Wen-Zhen Zhang, Zhen-Lin Producer: 20130325 In: Bone vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1004.	PD1 pathway in immune-mediated myopathies: Pathogenesis of dysfunctional T cells revisited. [electronic resource] by Knauss, Samuel Preusse, Corinna Allenbach, Yves Leonard-Louis, Sarah Touat, Mehdi Fischer, Norina Radbruch, Helena Mothes, Ronja Matyash, Vitali Böhmerle, Wolfgang Endres, Matthias Goebel, Hans-Hilmar Benveniste, Olivier Stenzel, Werner Producer: 20200924 In: Neurology(R) neuroimmunology & neuroinflammation vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1005.	Proteomic Profiling Unravels a Key Role of Specific Macrophage Subtypes in Sporadic Inclusion Body Myositis. [electronic resource] by Roos, Andreas Preusse, Corinna Hathazi, Denisa Goebel, Hans-Hilmar Stenzel, Werner Producer: 20200930 In: Frontiers in immunology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1006.	Transgenic mice expressing the human C99 terminal fragment of betaAPP: effects on cytochrome oxidase activity in skeletal muscle and brain. [electronic resource] by Strazielle, C Dumont, M Fukuchi, K Lalonde, R Producer: 20041018 In: Journal of chemical neuroanatomy vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1007.	Rabbits fed cholesterol-enriched diets exhibit pathological features of inclusion body myositis. [electronic resource] by Chen, Xuesong Ghribi, Othman Geiger, Jonathan D Producer: 20081031 In: American journal of physiology. Regulatory, integrative and comparative physiology vol. 294 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1008.	Seropositivity for NT5c1A antibody in sporadic inclusion body myositis predicts more severe motor, bulbar and respiratory involvement. [electronic resource] by Goyal, N A Cash, T M Alam, U Enam, S Tierney, P Araujo, N Mozaffar, F H Pestronk, A Mozaffar, T Producer: 20160725 In: Journal of neurology, neurosurgery, and psychiatry vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1009.	Beta-amyloid peptide expression is sufficient for myotube death: implications for human inclusion body myopathy. [electronic resource] by Querfurth, H W Suhara, T Rosen, K M McPhie, D L Fujio, Y Tejada, G Neve, R L Adelman, L S Walsh, K Producer: 20010809 In: Molecular and cellular neurosciences vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1010.	Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation. [electronic resource] by Bersano, Anna Del Bo, Roberto Lamperti, Costanza Ghezzi, Serena Fagiolari, Gigliola Fortunato, Francesco Ballabio, Elena Moggio, Maurizio Candelise, Livia Galimberti, Daniela Virgilio, Roberta Lanfranconi, Silvia Torrente, Yvan Carpo, Marinella Bresolin, Nereo Comi, Giacomo P Corti, Stefania Producer: 20090622 In: Neurobiology of aging vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1011.	Brain imaging and neuropsychology in late-onset dementia due to a novel mutation (R93C) of valosin-containing protein. [electronic resource] by Krause, S Göhringer, T Walter, M C Schoser, B G H Reilich, P Linn, J Pöpperl, G E Frölich, L Hentschel, F Lochmüller, H Danek, A Producer: 20071107 In: Clinical neuropathology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1012.	Sporadic inclusion-body myositis: conformational multifactorial ageing-related degenerative muscle disease associated with proteasomal and lysosomal inhibition, endoplasmic reticulum stress, and accumulation of amyloid-β42 oligomers and phosphorylated tau. [electronic resource] by Askanas, Valerie Engel, W King Producer: 20110615 In: Presse medicale (Paris, France : 1983) vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1013.	Diffusion-weighted magnetic resonance imaging is useful for assessing inflammatory myopathies. [electronic resource] by Faruch, Marie Garcia, Ana Isabel Del Amo, Montse Pomes, Jaume Isern, Jaime González, Sergio Prieto Grau, Josep María Milisenda, José César Tomas, Xavier Producer: 20191022 In: Muscle & nerve vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1014.	Expression of Bcl-2 in inclusion body myositis. [electronic resource] by Fyhr, Ing-Marie Lindberg, C Oldfors, A Producer: 20020712 In: Acta neurologica Scandinavica vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1015.	Normal in vivo skeletal muscle oxidative metabolism in sporadic inclusion body myositis assessed by 31P-magnetic resonance spectroscopy. [electronic resource] by Lodi, R Taylor, D J Tabrizi, S J Hilton-Jones, D Squier, M V Seller, A Styles, P Schapira, A H Producer: 19981204 In: Brain : a journal of neurology vol. 121 ( Pt 11) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1016.	Shared blood and muscle CD8+ T-cell expansions in inclusion body myositis. [electronic resource] by Dimitri, Dalia Benveniste, Olivier Dubourg, Odile Maisonobe, Thierry Eymard, Bruno Amoura, Zahir Jean, Laetitia Tiev, Kiet Piette, Jean-Charles Klatzmann, David Herson, Serge Boyer, Olivier Producer: 20060417 In: Brain : a journal of neurology vol. 129 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1017.	Sporadic inclusion body myositis: phenotypic variability and influence of HLA-DR3 in a cohort of 57 Australian cases. [electronic resource] by Needham, M James, I Corbett, A Day, T Christiansen, F Phillips, B Mastaglia, F L Producer: 20080903 In: Journal of neurology, neurosurgery, and psychiatry vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1018.	A novel autosomal dominant inclusion body myopathy linked to 7q22.1-31.1. [electronic resource] by Lu, Yan Li, Xingang Wang, Min Li, Xin Zhang, Feng Li, Yun Zhang, Meng Da, Yuwei Yu, Jun Jia, Jianping Producer: 20121212 In: PloS one vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1019.	A newly uncovered group of distantly related lysine methyltransferases preferentially interact with molecular chaperones to regulate their activity. [electronic resource] by Cloutier, Philippe Lavallée-Adam, Mathieu Faubert, Denis Blanchette, Mathieu Coulombe, Benoit Producer: 20130530 In: PLoS genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1020.	Investigation of splicing changes and post-translational processing of LMNA in sporadic inclusion body myositis. [electronic resource] by Luo, Yue-Bei Mitrpant, Chalermchai Johnsen, Russell Fabian, Vicki Needham, Merrilee Fletcher, Sue Wilton, Steve D Mastaglia, Frank L Producer: 20140418 In: International journal of clinical and experimental pathology vol. 6 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1136 results.