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Items: 1 to 20 of 31

1.

Experiences Of Individuals Concerning Combined Orthodontic and Orthognathic Surgical Treatment: A Qualitative Twitter Analysis.

Watts GD, Christou P, Antonarakis GS.

Med Princ Pract. 2018;27(3):227-235. doi: 10.1159/000487904. Epub 2018 Apr 11.

2.

Single versus segmental maxillary osteotomies and long-term stability in unilateral cleft lip and palate related malocclusion.

Watts GD, Antonarakis GS, Forrest CR, Tompson BD, Phillips JH.

J Oral Maxillofac Surg. 2014 Dec;72(12):2514-21. doi: 10.1016/j.joms.2014.07.005. Epub 2014 Jul 16.

PMID:
25262403
3.

Is Linear Advancement Related to Relapse in Unilateral Cleft Lip and Palate Orthognathic Surgery?

Watts GD, Antonarakis GS, Forrest CR, Tompson BD, Phillips JH.

Cleft Palate Craniofac J. 2015 Nov;52(6):717-23. doi: 10.1597/14-061.1. Epub 2014 Sep 26.

PMID:
25259777
4.

Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia.

Mehta SG, Khare M, Ramani R, Watts GD, Simon M, Osann KE, Donkervoort S, Dec E, Nalbandian A, Platt J, Pasquali M, Wang A, Mozaffar T, Smith CD, Kimonis VE.

Clin Genet. 2013 May;83(5):422-31. doi: 10.1111/cge.12000. Epub 2012 Oct 4.

5.

The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis.

Nalbandian A, Donkervoort S, Dec E, Badadani M, Katheria V, Rana P, Nguyen C, Mukherjee J, Caiozzo V, Martin B, Watts GD, Vesa J, Smith C, Kimonis VE.

J Mol Neurosci. 2011 Nov;45(3):522-31. doi: 10.1007/s12031-011-9627-y. Epub 2011 Sep 3. Review.

PMID:
21892620
6.

VCP associated inclusion body myopathy and paget disease of bone knock-in mouse model exhibits tissue pathology typical of human disease.

Badadani M, Nalbandian A, Watts GD, Vesa J, Kitazawa M, Su H, Tanaja J, Dec E, Wallace DC, Mukherjee J, Caiozzo V, Warman M, Kimonis VE.

PLoS One. 2010 Oct 5;5(10). pii: e13183. doi: 10.1371/journal.pone.0013183.

7.

A case of late-onset proximal and distal muscle weakness.

Barohn RJ, Watts GD, Amato AA.

Neurology. 2009 Nov 10;73(19):1592-7. doi: 10.1212/WNL.0b013e3181c0d4cb. No abstract available.

PMID:
19901252
8.

Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts.

Vesa J, Su H, Watts GD, Krause S, Walter MC, Martin B, Smith C, Wallace DC, Kimonis VE.

Neuromuscul Disord. 2009 Nov;19(11):766-72. doi: 10.1016/j.nmd.2009.08.003. Epub 2009 Oct 13.

9.

Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia.

Kimonis VE, Mehta SG, Fulchiero EC, Thomasova D, Pasquali M, Boycott K, Neilan EG, Kartashov A, Forman MS, Tucker S, Kimonis K, Mumm S, Whyte MP, Smith CD, Watts GD.

Am J Med Genet A. 2008 Mar 15;146A(6):745-57. doi: 10.1002/ajmg.a.31862.

10.

Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.

Watts GD, Thomasova D, Ramdeen SK, Fulchiero EC, Mehta SG, Drachman DA, Weihl CC, Jamrozik Z, Kwiecinski H, Kaminska A, Kimonis VE.

Clin Genet. 2007 Nov;72(5):420-6.

PMID:
17935506
11.

Nuclear localization of valosin-containing protein in normal muscle and muscle affected by inclusion-body myositis.

Greenberg SA, Watts GD, Kimonis VE, Amato AA, Pinkus JL.

Muscle Nerve. 2007 Oct;36(4):447-54.

PMID:
17626287
12.

APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD).

Mehta SG, Watts GD, Adamson JL, Hutton M, Umberger G, Xiong S, Ramdeen S, Lovell MA, Kimonis VE, Smith CD.

Genet Med. 2007 Jan;9(1):9-13.

PMID:
17224685
13.

Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations.

Forman MS, Mackenzie IR, Cairns NJ, Swanson E, Boyer PJ, Drachman DA, Jhaveri BS, Karlawish JH, Pestronk A, Smith TW, Tu PH, Watts GD, Markesbery WR, Smith CD, Kimonis VE.

J Neuropathol Exp Neurol. 2006 Jun;65(6):571-81.

PMID:
16783167
14.

Manifestations in a family with autosomal dominant bone fragility and limb-girdle myopathy.

Mehta SG, Watts GD, McGillivray B, Mumm S, Hamilton SJ, Ramdeen S, Novack D, Briggs C, Whyte MP, Kimonis VE.

Am J Med Genet A. 2006 Feb 15;140(4):322-30.

PMID:
16419137
15.

Autosomal dominant inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.

Kimonis VE, Watts GD.

Alzheimer Dis Assoc Disord. 2005 Oct-Dec;19 Suppl 1:S44-7.

PMID:
16317258
16.

Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22: a novel locus for a musculoskeletal syndrome.

Watts GD, Mehta SG, Zhao C, Ramdeen S, Hamilton SJ, Novack DV, Mumm S, Whyte MP, Mc Gillivray B, Kimonis VE.

Hum Genet. 2005 Dec;118(3-4):508-14. Epub 2005 Oct 22.

PMID:
16244874
17.

Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone.

Lucas GJ, Mehta SG, Hocking LJ, Stewart TL, Cundy T, Nicholson GC, Walsh JP, Fraser WD, Watts GD, Ralston SH, Kimonis VE.

Bone. 2006 Feb;38(2):280-5. Epub 2005 Sep 30.

PMID:
16199218
18.

Mutations in SEPT9 cause hereditary neuralgic amyotrophy.

Kuhlenbäumer G, Hannibal MC, Nelis E, Schirmacher A, Verpoorten N, Meuleman J, Watts GD, De Vriendt E, Young P, Stögbauer F, Halfter H, Irobi J, Goossens D, Del-Favero J, Betz BG, Hor H, Kurlemann G, Bird TD, Airaksinen E, Mononen T, Serradell AP, Prats JM, Van Broeckhoven C, De Jonghe P, Timmerman V, Ringelstein EB, Chance PF.

Nat Genet. 2005 Oct;37(10):1044-6. Epub 2005 Sep 25.

PMID:
16186812
19.

Mutant valosin-containing protein causes a novel type of frontotemporal dementia.

Schröder R, Watts GD, Mehta SG, Evert BO, Broich P, Fliessbach K, Pauls K, Hans VH, Kimonis V, Thal DR.

Ann Neurol. 2005 Mar;57(3):457-61.

PMID:
15732117
20.

Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophy.

Hünermund G, Schirmacher A, Ringelstein B, Young P, Watts GD, Meuleman J, Nelis E, Chance PF, Timmerman V, Stögbauer F, Kuhlenbäumer G.

Muscle Nerve. 2004 Apr;29(4):601-4.

PMID:
15052627

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