Burghes AH - Search Results

1

Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibers.

Klein CJ, Coovert DD, Bulman DE, Ray PN, Mendell JR, Burghes AH. Klein CJ, et al. Among authors: burghes ah. Am J Hum Genet. 1992 May;50(5):950-9. Am J Hum Genet. 1992. PMID: 1570844 Free PMC article.

2

Identification of a 2 base pair nonsense mutation causing a cryptic splice site in a DMD patient.

Winnard AV, Jia-Hsu Y, Gibbs RA, Mendell JR, Burghes AH. Winnard AV, et al. Among authors: burghes ah. Hum Mol Genet. 1992 Nov;1(8):645-6. doi: 10.1093/hmg/1.8.645. Hum Mol Genet. 1992. PMID: 1301174 No abstract available.

3

A HindIII/BglII dystrophin gene polymorphism in the African-American population.

Prior TW, Papp AC, Snyder PJ, Burghes AH, Wallace BH. Prior TW, et al. Among authors: burghes ah. Hum Genet. 1992 Aug;89(6):687-8. doi: 10.1007/BF00221965. Hum Genet. 1992. PMID: 1355070

4

Dystrophin expression and somatic reversion in prednisone-treated and untreated Duchenne dystrophy. CIDD Study Group.

Burrow KL, Coovert DD, Klein CJ, Bulman DE, Kissel JT, Rammohan KW, Burghes AH, Mendell JR. Burrow KL, et al. Among authors: burghes ah. Neurology. 1991 May;41(5):661-6. doi: 10.1212/wnl.41.5.661. Neurology. 1991. PMID: 1781820 Clinical Trial.

5

Duchenne muscular dystrophy gene expression in normal and diseased human muscle.

Scott MO, Sylvester JE, Heiman-Patterson T, Shi YJ, Fieles W, Stedman H, Burghes A, Ray P, Worton R, Fischbeck KH. Scott MO, et al. Science. 1988 Mar 18;239(4846):1418-20. doi: 10.1126/science.2450401. Science. 1988. PMID: 2450401

6

Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene.

Gillard EF, Chamberlain JS, Murphy EG, Duff CL, Smith B, Burghes AH, Thompson MW, Sutherland J, Oss I, Bodrug SE, et al. Gillard EF, et al. Among authors: burghes ah. Am J Hum Genet. 1989 Oct;45(4):507-20. Am J Hum Genet. 1989. PMID: 2491010 Free PMC article.

7

Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy gene.

Hu XY, Burghes AH, Bulman DE, Ray PN, Worton RG. Hu XY, et al. Among authors: burghes ah. Am J Hum Genet. 1989 Jun;44(6):855-63. Am J Hum Genet. 1989. PMID: 2567117 Free PMC article.

8

The problem of Duchenne muscular dystrophy.

Worton RG, Ray PN, Bodrug S, Burghes AH, Hu X, Thompson MW. Worton RG, et al. Among authors: burghes ah. Philos Trans R Soc Lond B Biol Sci. 1988 Jun 15;319(1194):275-84. doi: 10.1098/rstb.1988.0049. Philos Trans R Soc Lond B Biol Sci. 1988. PMID: 2900521 Review.

9

Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy.

Malhotra SB, Hart KA, Klamut HJ, Thomas NS, Bodrug SE, Burghes AH, Bobrow M, Harper PS, Thompson MW, Ray PN, et al. Malhotra SB, et al. Among authors: burghes ah. Science. 1988 Nov 4;242(4879):755-9. doi: 10.1126/science.3055295. Science. 1988. PMID: 3055295

10

The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle.

Zubrzycka-Gaarn EE, Bulman DE, Karpati G, Burghes AH, Belfall B, Klamut HJ, Talbot J, Hodges RS, Ray PN, Worton RG. Zubrzycka-Gaarn EE, et al. Among authors: burghes ah. Nature. 1988 Jun 2;333(6172):466-9. doi: 10.1038/333466a0. Nature. 1988. PMID: 3287171

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