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	1.	Monitoring autophagy in the treatment of protein aggregate diseases: steps toward identifying autophagic biomarkers. [electronic resource] by Weihl, Conrad C Producer: 20140210 In: Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Another VCP interactor: NF is enough. [electronic resource] by Weihl, Conrad C Producer: 20120131 In: The Journal of clinical investigation vol. 121 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Sporadic Inclusion Body Myositis and Other Rimmed Vacuolar Myopathies. [electronic resource] by Weihl, Conrad C Producer: 20200420 In: Continuum (Minneapolis, Minn.) vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Sporadic inclusion body myositis: possible pathogenesis inferred from biomarkers. [electronic resource] by Weihl, Conrad C Pestronk, Alan Producer: 20101214 In: Current opinion in neurology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	The VCP/p97 system at a glance: connecting cellular function to disease pathogenesis. [electronic resource] by Meyer, Hemmo Weihl, Conrad C Producer: 20150622 In: Journal of cell science vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Motor neuron disease associated with copper deficiency. [electronic resource] by Weihl, Conrad C Lopate, Glenn Producer: 20070302 In: Muscle & nerve vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Regulation of SQSTM1/p62 via UBA domain ubiquitination and its role in disease. [electronic resource] by Lee, YouJin Weihl, Conrad C Producer: 20180521 In: Autophagy vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagy. [electronic resource] by Ju, Jeong-Sun Weihl, Conrad C Producer: 20100824 In: Human molecular genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	p97/VCP at the intersection of the autophagy and the ubiquitin proteasome system. [electronic resource] by Ju, Jeong-Sun Weihl, Conrad C Producer: 20100706 In: Autophagy vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Establishing prevalence in rare neuromuscular diseases: A lesson from congenital myopathies. [electronic resource] by Bamaga, Ahmed K Weihl, Conrad C Publication details: Neurology. Genetics Apr 2017 In: Neurology. Genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Rapamycin-induced autophagy aggravates pathology and weakness in a mouse model of VCP-associated myopathy. [electronic resource] by Ching, James K Weihl, Conrad C Producer: 20131122 In: Autophagy vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Inflammatory myopathies with mitochondrial pathology and protein aggregates. [electronic resource] by Temiz, Peyker Weihl, Conrad C Pestronk, Alan Producer: 20090504 In: Journal of the neurological sciences vol. 278 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	234th ENMC International Workshop: Chaperone dysfunction in muscle disease Naarden, The Netherlands, 8-10 December 2017. [electronic resource] by Weihl, Conrad C Udd, Bjarne Hanna, Michael Producer: 20191023 In: Neuromuscular disorders : NMD vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia. [electronic resource] by Weihl, Conrad C Pestronk, Alan Kimonis, Virginia E Producer: 20090728 In: Neuromuscular disorders : NMD vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Valproate may improve strength and function in patients with type III/IV spinal muscle atrophy. [electronic resource] by Weihl, Conrad C Connolly, Anne M Pestronk, Alan Producer: 20060906 In: Neurology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Mitochondrial pathology in immune and inflammatory myopathies. [electronic resource] by Varadhachary, Arun S Weihl, Conrad C Pestronk, Alan Producer: 20110628 In: Current opinion in rheumatology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	215th ENMC International Workshop VCP-related multi-system proteinopathy (IBMPFD) 13-15 November 2015, Heemskerk, The Netherlands. [electronic resource] by Evangelista, Teresinha Weihl, Conrad C Kimonis, Virginia Lochmüller, Hanns Producer: 20180301 In: Neuromuscular disorders : NMD vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation. [electronic resource] by Weihl, Conrad C Dalal, Seema Pestronk, Alan Hanson, Phyllis I Producer: 20060712 In: Human molecular genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathy. [electronic resource] by Findlay, Andrew R Harms, Matthew B Pestronk, Alan Weihl, Conrad C Producer: 20191023 In: Neuromuscular disorders : NMD vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice. [electronic resource] by Weihl, Conrad C Miller, Sara E Hanson, Phyllis I Pestronk, Alan Producer: 20070731 In: Human molecular genetics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 76 results.