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	1.	Molecular basis of hereditary neuropathies. [electronic resource] by Watts, Giles D J Chance, Phillip F Producer: 20020903 In: Advances in neurology vol. 88 Availability: No items available. Save to lists Add to cart (remove)
	2.	Autosomal dominant inclusion body myopathy, Paget disease of bone, and frontotemporal dementia. [electronic resource] by Kimonis, Virginia E Watts, Giles D J Producer: 20060411 In: Alzheimer disease and associated disorders vol. 19 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Vaginal ectopic ureter: a continuing diagnostic challenge. [electronic resource] by Giles, D J Nixon, G W Middleton, A W Producer: 19820924 In: The Western journal of medicine vol. 136 Availability: No items available. Save to lists Add to cart (remove)
	4.	Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families. [electronic resource] by Watts, Giles D J O'Briant, Kathy C Chance, Phillip F Producer: 20020516 In: Human genetics vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A case of late-onset proximal and distal muscle weakness. [electronic resource] by Barohn, Richard J Watts, Giles D J Amato, Anthony A Producer: 20091130 In: Neurology vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes. [electronic resource] by Watts, Giles D J Thorne, M Kovach, M J Pestronk, A Kimonis, Virginia E Producer: 20031007 In: Neuromuscular disorders : NMD vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. [electronic resource] by Watts, Giles D J Wymer, Jill Kovach, Margaret J Mehta, Sarju G Mumm, Steven Darvish, Daniel Pestronk, Alan Whyte, Michael P Kimonis, Virginia E Producer: 20040816 In: Nature genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Lumbar spine: pretest predictability of CT findings. [electronic resource] by Giles, D J Thomas, R J Osborn, A G Clayton, P D Miller, M H Bahr, A L Frederick, P R O'Connor, G D Ostler, D Producer: 19840323 In: Radiology vol. 150 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Manifestations in a family with autosomal dominant bone fragility and limb-girdle myopathy. [electronic resource] by Mehta, Sarju G Watts, Giles D J McGillivray, Barbara Mumm, Steven Hamilton, Sara Jane Ramdeen, Sheena Novack, Deborah Briggs, Christine Whyte, Michael P Kimonis, Virginia E Producer: 20060323 In: American journal of medical genetics. Part A vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Mutant valosin-containing protein causes a novel type of frontotemporal dementia. [electronic resource] by Schröder, Rolf Watts, Giles D J Mehta, Sarju G Evert, Bernd O Broich, Petra Fliessbach, Klaus Pauls, Katharina Hans, Volkmar H Kimonis, Virginia Thal, Dietmar R Producer: 20050425 In: Annals of neurology vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD). [electronic resource] by Mehta, Sarju G Watts, Giles D J Adamson, Jennifer L Hutton, Mike Umberger, Geanie Xiong, Shuling Ramdeen, Sheena Lovell, Mark A Kimonis, Virginia E Smith, Charles D Producer: 20070301 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22: a novel locus for a musculoskeletal syndrome. [electronic resource] by Watts, Giles D J Mehta, Sarju G Zhao, Chengfeng Ramdeen, Sheena Hamilton, Sara Jane Novack, Deborah V Mumm, Steven Whyte, Michael P Mc Gillivray, Barbara Kimonis, Virginia E Producer: 20060321 In: Human genetics vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone. [electronic resource] by Lucas, Gavin J A Mehta, Sarju G Hocking, Lynne J Stewart, Tracy L Cundy, Tim Nicholson, Geoff C Walsh, John P Fraser, William D Watts, Giles D J Ralston, Stuart H Kimonis, Virginia E Producer: 20060810 In: Bone vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia. [electronic resource] by Kimonis, Virginia E Mehta, Sarju G Fulchiero, Erin C Thomasova, Dana Pasquali, Marzia Boycott, Kym Neilan, Edward G Kartashov, Alex Forman, Mark S Tucker, Stuart Kimonis, Katerina Mumm, Steven Whyte, Michael P Smith, Charles D Watts, Giles D J Producer: 20080416 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations. [electronic resource] by Forman, Mark S Mackenzie, Ian R Cairns, Nigel J Swanson, Eric Boyer, Philip J Drachman, David A Jhaveri, Bharati S Karlawish, Jason H Pestronk, Alan Smith, Thomas W Tu, Pang-Hsien Watts, Giles D J Markesbery, William R Smith, Charles D Kimonis, Virginia E Producer: 20060804 In: Journal of neuropathology and experimental neurology vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Mutations in SEPT9 cause hereditary neuralgic amyotrophy. [electronic resource] by Kuhlenbäumer, Gregor Hannibal, Mark C Nelis, Eva Schirmacher, Anja Verpoorten, Nathalie Meuleman, Jan Watts, Giles D J De Vriendt, Els Young, Peter Stögbauer, Florian Halfter, Hartmut Irobi, Joy Goossens, Dirk Del-Favero, Jurgen Betz, Benjamin G Hor, Hyun Kurlemann, Gert Bird, Thomas D Airaksinen, Eila Mononen, Tarja Serradell, Adolfo Pou Prats, José M Van Broeckhoven, Christine De Jonghe, Peter Timmerman, Vincent Ringelstein, E Bernd Chance, Phillip F Producer: 20051220 In: Nature genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)