Wilcox DE - Search Results

1

Somatic instability of the expanded CTG triplet repeat in myotonic dystrophy type 1 is a heritable quantitative trait and modifier of disease severity.

Morales F, Couto JM, Higham CF, Hogg G, Cuenca P, Braida C, Wilson RH, Adam B, del Valle G, Brian R, Sittenfeld M, Ashizawa T, Wilcox A, Wilcox DE, Monckton DG. Morales F, et al. Among authors: wilcox de, wilcox a. Hum Mol Genet. 2012 Aug 15;21(16):3558-67. doi: 10.1093/hmg/dds185. Epub 2012 May 16. Hum Mol Genet. 2012. PMID: 22595968

2

Life expectancy and death from cardiomyopathy amongst carriers of Duchenne and Becker muscular dystrophy in Scotland.

Holloway SM, Wilcox DE, Wilcox A, Dean JC, Berg JN, Goudie DR, Denvir MA, Porteous ME. Holloway SM, et al. Among authors: wilcox de, wilcox a. Heart. 2008 May;94(5):633-6. doi: 10.1136/hrt.2007.125948. Epub 2007 Oct 11. Heart. 2008. PMID: 17932095

3

Palmoplantar keratoderma, nail dystrophy, and hereditary motor and sensory neuropathy: an autosomal dominant trait.

Tolmie JL, Wilcox DE, McWilliam R, Assindi A, Stephenson JB. Tolmie JL, et al. Among authors: wilcox de. J Med Genet. 1988 Nov;25(11):754-7. doi: 10.1136/jmg.25.11.754. J Med Genet. 1988. PMID: 2976839 Free PMC article.

4

Results of Duchenne muscular dystrophy family screening in practice: leaks rather than cascades?

McGowan R, Challoner BR, Ross S, Holloway S, Joss S, Wilcox D, Holden ST, Tolmie J, Longman C. McGowan R, et al. Clin Genet. 2013 Feb;83(2):187-90. doi: 10.1111/j.1399-0004.2012.01876.x. Epub 2012 Apr 9. Clin Genet. 2013. PMID: 22428906

5

99th ENMC international workshop: myotonic dystrophy: present management, future therapy. 9-11 November 2001, Naarden, The Netherlands.

Harper PS, van Engelen BG, Eymard B, Rogers M, Wilcox D. Harper PS, et al. Neuromuscul Disord. 2002 Aug;12(6):596-9. doi: 10.1016/s0960-8966(02)00020-2. Neuromuscul Disord. 2002. PMID: 12117486 No abstract available.

6

Modafinil for excessive daytime sleepiness in myotonic dystrophy type 1--the patients' perspective.

Hilton-Jones D, Bowler M, Lochmueller H, Longman C, Petty R, Roberts M, Rogers M, Turner C, Wilcox D. Hilton-Jones D, et al. Neuromuscul Disord. 2012 Jul;22(7):597-603. doi: 10.1016/j.nmd.2012.02.005. Epub 2012 Mar 16. Neuromuscul Disord. 2012. PMID: 22425060

7

Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry.

Wilcox DE, Cooke A, Colgan J, Boyd E, Aitken DA, Sinclair L, Glasgow L, Stephenson JB, Ferguson-Smith MA. Wilcox DE, et al. Hum Genet. 1986 Jun;73(2):175-80. doi: 10.1007/BF00291610. Hum Genet. 1986. PMID: 3721503

8

Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes.

Cooke A, Lanyon WG, Wilcox DE, Dornan ES, Kataki A, Gillard EF, McWhinnie AJ, Morris A, Ferguson-Smith MA, Connor JM. Cooke A, et al. Among authors: wilcox de. J Med Genet. 1990 May;27(5):292-7. doi: 10.1136/jmg.27.5.292. J Med Genet. 1990. PMID: 2191136 Free PMC article.

9

123rd ENMC International Workshop: management and therapy in myotonic dystrophy, 6-8 February 2004, Naarden, The Netherlands.

van Engelen BG, Eymard B, Wilcox D. van Engelen BG, et al. Neuromuscul Disord. 2005 May;15(5):389-94. doi: 10.1016/j.nmd.2005.02.001. Neuromuscul Disord. 2005. PMID: 15833434 No abstract available.

10

Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy.

Wilcox DE, Affara NA, Yates JR, Ferguson-Smith MA, Pearson PL. Wilcox DE, et al. Hum Genet. 1985;70(4):365-75. doi: 10.1007/BF00295379. Hum Genet. 1985. PMID: 3860471

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