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Nemaline myopathy caused by absence of alpha-skeletal muscle actin.
Nowak KJ, Sewry CA, Navarro C, Squier W, Reina C, Ricoy JR, Jayawant SS, Childs AM, Dobbie JA, Appleton RE, Mountford RC, Walker KR, Clement S, Barois A, Muntoni F, Romero NB, Laing NG. Nowak KJ, et al. Among authors: walker kr. Ann Neurol. 2007 Feb;61(2):175-84. doi: 10.1002/ana.21035. Ann Neurol. 2007. PMID: 17187373
Adenovirus and adeno-associated virus-mediated delivery of human myophosphorylase cDNA and LacZ cDNA to muscle in the ovine model of McArdle's disease: expression and re-expression of glycogen phosphorylase.
Howell JM, Walker KR, Davies L, Dunton E, Everaardt A, Laing N, Karpati G. Howell JM, et al. Among authors: walker kr. Neuromuscul Disord. 2008 Mar;18(3):248-58. doi: 10.1016/j.nmd.2007.10.006. Epub 2008 Mar 14. Neuromuscul Disord. 2008. PMID: 18343113
Disease severity and thin filament regulation in M9R TPM3 nemaline myopathy.
Ilkovski B, Mokbel N, Lewis RA, Walker K, Nowak KJ, Domazetovska A, Laing NG, Fowler VM, North KN, Cooper ST. Ilkovski B, et al. J Neuropathol Exp Neurol. 2008 Sep;67(9):867-77. doi: 10.1097/NEN.0b013e318183a44f. J Neuropathol Exp Neurol. 2008. PMID: 18716557 Free PMC article.
Actin mutations are one cause of congenital fibre type disproportion.
Laing NG, Clarke NF, Dye DE, Liyanage K, Walker KR, Kobayashi Y, Shimakawa S, Hagiwara T, Ouvrier R, Sparrow JC, Nishino I, North KN, Nonaka I. Laing NG, et al. Among authors: walker kr. Ann Neurol. 2004 Nov;56(5):689-94. doi: 10.1002/ana.20260. Ann Neurol. 2004. PMID: 15468086
UCI EyeMobile Exam Findings from School Children Following on-Site Screening.
Hong JD, Choi EH, Suh S, Bui JH, Storch AM, Walker KR, Shahraki K, Yanez C, Torres D, Espinoza J, Molina I, Suh DW. Hong JD, et al. Among authors: walker kr. Clin Ophthalmol. 2024 Jun 6;18:1667-1678. doi: 10.2147/OPTH.S460879. eCollection 2024. Clin Ophthalmol. 2024. PMID: 38860118 Free PMC article.
49 results