Brown SC - Search Results

1

Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteins.

Muntoni F, Bonne G, Goldfarb LG, Mercuri E, Piercy RJ, Burke M, Yaou RB, Richard P, Récan D, Shatunov A, Sewry CA, Brown SC. Muntoni F, et al. Among authors: brown sc. Brain. 2006 May;129(Pt 5):1260-8. doi: 10.1093/brain/awl062. Epub 2006 Apr 3. Brain. 2006. PMID: 16585054

2

Congenital muscular dystrophies.

Mercuri E, Sewry C, Brown SC, Muntoni F. Mercuri E, et al. Among authors: brown sc. Semin Pediatr Neurol. 2002 Jun;9(2):120-31. doi: 10.1053/spen.2002.33802. Semin Pediatr Neurol. 2002. PMID: 12138996 Review.

3

Desmin immunolocalisation in autosomal dominant Emery-Dreifuss muscular dystrophy.

Piercy RJ, Zhou H, Feng L, Pombo A, Muntoni F, Brown SC. Piercy RJ, et al. Among authors: brown sc. Neuromuscul Disord. 2007 Apr;17(4):297-305. doi: 10.1016/j.nmd.2007.01.003. Epub 2007 Feb 27. Neuromuscul Disord. 2007. PMID: 17329105

4

Investigating the pathology of Emery-Dreifuss muscular dystrophy.

Brown SC, Piercy RJ, Muntoni F, Sewry CA. Brown SC, et al. Biochem Soc Trans. 2008 Dec;36(Pt 6):1335-8. doi: 10.1042/BST0361335. Biochem Soc Trans. 2008. PMID: 19021551 Review.

5

Reduced expression of fukutin related protein in mice results in a model for fukutin related protein associated muscular dystrophies.

Ackroyd MR, Skordis L, Kaluarachchi M, Godwin J, Prior S, Fidanboylu M, Piercy RJ, Muntoni F, Brown SC. Ackroyd MR, et al. Among authors: brown sc. Brain. 2009 Feb;132(Pt 2):439-51. doi: 10.1093/brain/awn335. Epub 2009 Jan 20. Brain. 2009. PMID: 19155270

6

Non-sarcolemmal muscular dystrophies.

Brown SC, Muntoni F, Sewry CA. Brown SC, et al. Brain Pathol. 2001 Apr;11(2):193-205. doi: 10.1111/j.1750-3639.2001.tb00392.x. Brain Pathol. 2001. PMID: 11303795 Free PMC article. Review.

7

Skeletal muscle pathology in autosomal dominant Emery-Dreifuss muscular dystrophy with lamin A/C mutations.

Sewry CA, Brown SC, Mercuri E, Bonne G, Feng L, Camici G, Morris GE, Muntoni F. Sewry CA, et al. Among authors: brown sc. Neuropathol Appl Neurobiol. 2001 Aug;27(4):281-90. doi: 10.1046/j.0305-1846.2001.00323.x. Neuropathol Appl Neurobiol. 2001. PMID: 11532159

8

Collagen VI involvement in Ullrich syndrome: a clinical, genetic, and immunohistochemical study.

Mercuri E, Yuva Y, Brown SC, Brockington M, Kinali M, Jungbluth H, Feng L, Sewry CA, Muntoni F. Mercuri E, et al. Among authors: brown sc. Neurology. 2002 May 14;58(9):1354-9. doi: 10.1212/wnl.58.9.1354. Neurology. 2002. PMID: 12011280

9

Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores.

Jungbluth H, Müller CR, Halliger-Keller B, Brockington M, Brown SC, Feng L, Chattopadhyay A, Mercuri E, Manzur AY, Ferreiro A, Laing NG, Davis MR, Roper HP, Dubowitz V, Bydder G, Sewry CA, Muntoni F. Jungbluth H, et al. Among authors: brown sc. Neurology. 2002 Jul 23;59(2):284-7. doi: 10.1212/wnl.59.2.284. Neurology. 2002. PMID: 12136074

10

Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene.

Mercuri E, Brown SC, Nihoyannopoulos P, Poulton J, Kinali M, Richard P, Piercy RJ, Messina S, Sewry C, Burke MM, McKenna W, Bonne G, Muntoni F. Mercuri E, et al. Among authors: brown sc. Muscle Nerve. 2005 May;31(5):602-9. doi: 10.1002/mus.20293. Muscle Nerve. 2005. PMID: 15770669

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