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Exon skipping and translation in patients with frameshift deletions in the dystrophin gene.
Sherratt TG, Vulliamy T, Dubowitz V, Sewry CA, Strong PN. Sherratt TG, et al. Among authors: sewry ca. Am J Hum Genet. 1993 Nov;53(5):1007-15. Am J Hum Genet. 1993. PMID: 8213828 Free PMC article.
Binding of Ricinus communis I lectin to developing dystrophic muscle in human fetus.
Voit T, Sewry CA, Dunn MJ, Dubowitz V. Voit T, et al. Among authors: sewry ca. J Neurol Sci. 1988 Apr;84(2-3):301-14. doi: 10.1016/0022-510x(88)90134-7. J Neurol Sci. 1988. PMID: 3379448
Muscular dystrophies due to defective glycosylation of dystroglycan.
Muntoni F, Brockington M, Godfrey C, Ackroyd M, Robb S, Manzur A, Kinali M, Mercuri E, Kaluarachchi M, Feng L, Jimenez-Mallebrera C, Clement E, Torelli S, Sewry CA, Brown SC. Muntoni F, et al. Among authors: sewry ca. Acta Myol. 2007 Dec;26(3):129-35. Acta Myol. 2007. PMID: 18646561 Free PMC article. Review.
Mutations in the laminin alpha2-chain gene in two children with early-onset muscular dystrophy.
Naom I, D'alessandro M, Sewry CA, Jardine P, Ferlini A, Moss T, Dubowitz V, Muntoni F. Naom I, et al. Among authors: sewry ca. Brain. 2000 Jan;123 ( Pt 1):31-41. doi: 10.1093/brain/123.1.31. Brain. 2000. PMID: 10611118
Immunocytochemical analysis of human muscular dystrophy.
Sewry CA. Sewry CA. Microsc Res Tech. 2000 Feb 1-15;48(3-4):142-54. doi: 10.1002/(SICI)1097-0029(20000201/15)48:3/4<142::AID-JEMT3>3.0.CO;2-9. Microsc Res Tech. 2000. PMID: 10679962 Review.
Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy.
Naom I, D'Alessandro M, Sewry CA, Philpot J, Manzur AY, Dubowitz V, Muntoni F. Naom I, et al. Among authors: sewry ca. Neuromuscul Disord. 1998 Oct;8(7):495-501. doi: 10.1016/s0960-8966(98)00065-0. Neuromuscul Disord. 1998. PMID: 9829280
Mutations in Emery-Dreifuss muscular dystrophy and their effects on emerin protein expression.
Manilal S, Recan D, Sewry CA, Hoeltzenbein M, Llense S, Leturcq F, Deburgrave N, Barbot J, Man N, Muntoni F, Wehnert M, Kaplan J, Morris GE. Manilal S, et al. Among authors: sewry ca. Hum Mol Genet. 1998 May;7(5):855-64. doi: 10.1093/hmg/7.5.855. Hum Mol Genet. 1998. PMID: 9536090
The abnormal expression of utrophin in Duchenne and Becker muscular dystrophy is age related.
Taylor J, Muntoni F, Dubowitz V, Sewry CA. Taylor J, et al. Among authors: sewry ca. Neuropathol Appl Neurobiol. 1997 Oct;23(5):399-405. Neuropathol Appl Neurobiol. 1997. PMID: 9364465
Characterization of genetic deletions in Becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophin.
Le Thiet Thanh, Nguyen Thi Man, Hori S, Sewry CA, Dubowitz V, Morris GE. Le Thiet Thanh, et al. Among authors: sewry ca. Am J Med Genet. 1995 Aug 28;58(2):177-86. doi: 10.1002/ajmg.1320580217. Am J Med Genet. 1995. PMID: 8533812
Long mutant dystrophins and variable phenotypes: evasion of nonsense-mediated decay?
Kerr TP, Sewry CA, Robb SA, Roberts RG. Kerr TP, et al. Among authors: sewry ca. Hum Genet. 2001 Oct;109(4):402-7. doi: 10.1007/s004390100598. Hum Genet. 2001. PMID: 11702221
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