Brown SC - Search Results

1

Relocalization of neuronal nitric oxide synthase (nNOS) as a marker for complete restoration of the dystrophin associated protein complex in skeletal muscle.

Wells KE, Torelli S, Lu Q, Brown SC, Partridge T, Muntoni F, Wells DJ. Wells KE, et al. Among authors: brown sc. Neuromuscul Disord. 2003 Jan;13(1):21-31. doi: 10.1016/s0960-8966(02)00191-8. Neuromuscul Disord. 2003. PMID: 12467729

2

Muscle development genes: their relevance in neuromuscular disorders.

Muntoni F, Brown S, Sewry C, Patel K. Muntoni F, et al. Neuromuscul Disord. 2002 Jun;12(5):438-46. doi: 10.1016/s0960-8966(01)00326-1. Neuromuscul Disord. 2002. PMID: 12031617 Review.

3

Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the human.

Neri M, Torelli S, Brown S, Ugo I, Sabatelli P, Merlini L, Spitali P, Rimessi P, Gualandi F, Sewry C, Ferlini A, Muntoni F. Neri M, et al. Neuromuscul Disord. 2007 Dec;17(11-12):913-8. doi: 10.1016/j.nmd.2007.07.005. Epub 2007 Sep 7. Neuromuscul Disord. 2007. PMID: 17826093

4

Sub-cellular localisation of fukutin related protein in different cell lines and in the muscle of patients with MDC1C and LGMD2I.

Torelli S, Brown SC, Brockington M, Dolatshad NF, Jimenez C, Skordis L, Feng LH, Merlini L, Jones DH, Romero N, Wewer U, Voit T, Sewry CA, Noguchi S, Nishino I, Muntoni F. Torelli S, et al. Among authors: brown sc. Neuromuscul Disord. 2005 Dec;15(12):836-43. doi: 10.1016/j.nmd.2005.09.004. Epub 2005 Nov 8. Neuromuscul Disord. 2005. PMID: 16288869

5

Absence of neuronal nitric oxide synthase (nNOS) as a pathological marker for the diagnosis of Becker muscular dystrophy with rod domain deletions.

Torelli S, Brown SC, Jimenez-Mallebrera C, Feng L, Muntoni F, Sewry CA. Torelli S, et al. Among authors: brown sc. Neuropathol Appl Neurobiol. 2004 Oct;30(5):540-5. doi: 10.1111/j.1365-2990.2004.00561.x. Neuropathol Appl Neurobiol. 2004. PMID: 15488030

6

A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of alpha-dystroglycan.

Dinçer P, Balci B, Yuva Y, Talim B, Brockington M, Dinçel D, Torelli S, Brown S, Kale G, Haliloglu G, Gerçeker FO, Atalay RC, Yakicier C, Longman C, Muntoni F, Topaloglu H. Dinçer P, et al. Neuromuscul Disord. 2003 Dec;13(10):771-8. doi: 10.1016/s0960-8966(03)00161-5. Neuromuscul Disord. 2003. PMID: 14678799

7

Defective glycosylation in muscular dystrophy.

Muntoni F, Brockington M, Blake DJ, Torelli S, Brown SC. Muntoni F, et al. Among authors: brown sc. Lancet. 2002 Nov 2;360(9343):1419-21. doi: 10.1016/S0140-6736(02)11397-3. Lancet. 2002. PMID: 12424008 Review.

8

Phenotypic spectrum associated with mutations in the fukutin-related protein gene.

Mercuri E, Brockington M, Straub V, Quijano-Roy S, Yuva Y, Herrmann R, Brown SC, Torelli S, Dubowitz V, Blake DJ, Romero NB, Estournet B, Sewry CA, Guicheney P, Voit T, Muntoni F. Mercuri E, et al. Among authors: brown sc. Ann Neurol. 2003 Apr;53(4):537-42. doi: 10.1002/ana.10559. Ann Neurol. 2003. PMID: 12666124

9

Profound skeletal muscle depletion of alpha-dystroglycan in Walker-Warburg syndrome.

Jiménez-Mallebrera C, Torelli S, Brown SC, Feng L, Brockington M, Sewry CA, Beltrán-Valero De Bernabé D, Muntoni F. Jiménez-Mallebrera C, et al. Among authors: brown sc. Eur J Paediatr Neurol. 2003;7(3):129-37. doi: 10.1016/s1090-3798(03)00042-4. Eur J Paediatr Neurol. 2003. PMID: 12788039

10

Abnormalities in alpha-dystroglycan expression in MDC1C and LGMD2I muscular dystrophies.

Brown SC, Torelli S, Brockington M, Yuva Y, Jimenez C, Feng L, Anderson L, Ugo I, Kroger S, Bushby K, Voit T, Sewry C, Muntoni F. Brown SC, et al. Am J Pathol. 2004 Feb;164(2):727-37. doi: 10.1016/s0002-9440(10)63160-4. Am J Pathol. 2004. PMID: 14742276 Free PMC article.

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