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The structure of the N-terminal actin-binding domain of human dystrophin and how mutations in this domain may cause Duchenne or Becker muscular dystrophy.
Norwood FL, Sutherland-Smith AJ, Keep NH, Kendrick-Jones J. Norwood FL, et al. Structure. 2000 May 15;8(5):481-91. doi: 10.1016/s0969-2126(00)00132-5. Structure. 2000. PMID: 10801490 Free article.
An atomic model for actin binding by the CH domains and spectrin-repeat modules of utrophin and dystrophin.
Sutherland-Smith AJ, Moores CA, Norwood FL, Hatch V, Craig R, Kendrick-Jones J, Lehman W. Sutherland-Smith AJ, et al. Among authors: norwood fl. J Mol Biol. 2003 May 23;329(1):15-33. doi: 10.1016/s0022-2836(03)00422-4. J Mol Biol. 2003. PMID: 12742015
The 2.0 A structure of the second calponin homology domain from the actin-binding region of the dystrophin homologue utrophin.
Keep NH, Norwood FL, Moores CA, Winder SJ, Kendrick-Jones J. Keep NH, et al. Among authors: norwood fl. J Mol Biol. 1999 Jan 22;285(3):1257-64. doi: 10.1006/jmbi.1998.2406. J Mol Biol. 1999. PMID: 9887274
Crystal structure of the actin-binding region of utrophin reveals a head-to-tail dimer.
Keep NH, Winder SJ, Moores CA, Walke S, Norwood FL, Kendrick-Jones J. Keep NH, et al. Among authors: norwood fl. Structure. 1999 Dec 15;7(12):1539-46. doi: 10.1016/s0969-2126(00)88344-6. Structure. 1999. PMID: 10647184 Free article.
Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy.
Winter L, Türk M, Harter PN, Mittelbronn M, Kornblum C, Norwood F, Jungbluth H, Thiel CT, Schlötzer-Schrehardt U, Schröder R. Winter L, et al. Among authors: norwood f. Acta Neuropathol Commun. 2016 Apr 27;4(1):44. doi: 10.1186/s40478-016-0314-7. Acta Neuropathol Commun. 2016. PMID: 27121971 Free PMC article.
EFNS guideline on diagnosis and management of limb girdle muscular dystrophies.
Norwood F, de Visser M, Eymard B, Lochmüller H, Bushby K; EFNS Guideline Task Force. Norwood F, et al. Eur J Neurol. 2007 Dec;14(12):1305-12. doi: 10.1111/j.1468-1331.2007.01979.x. Eur J Neurol. 2007. PMID: 18028188 Review.
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis.
Dlamini N, Voermans NC, Lillis S, Stewart K, Kamsteeg EJ, Drost G, Quinlivan R, Snoeck M, Norwood F, Radunovic A, Straub V, Roberts M, Vrancken AF, van der Pol WL, de Coo RI, Manzur AY, Yau S, Abbs S, King A, Lammens M, Hopkins PM, Mohammed S, Treves S, Muntoni F, Wraige E, Davis MR, van Engelen B, Jungbluth H. Dlamini N, et al. Among authors: norwood f. Neuromuscul Disord. 2013 Jul;23(7):540-8. doi: 10.1016/j.nmd.2013.03.008. Epub 2013 Apr 28. Neuromuscul Disord. 2013. PMID: 23628358
Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population.
Norwood FL, Harling C, Chinnery PF, Eagle M, Bushby K, Straub V. Norwood FL, et al. Brain. 2009 Nov;132(Pt 11):3175-86. doi: 10.1093/brain/awp236. Epub 2009 Sep 18. Brain. 2009. PMID: 19767415 Free PMC article.
179th ENMC international workshop: pregnancy in women with neuromuscular disorders 5-7 November 2010, Naarden, The Netherlands.
Norwood F, Rudnik-Schöneborn S. Norwood F, et al. Neuromuscul Disord. 2012 Feb;22(2):183-90. doi: 10.1016/j.nmd.2011.05.009. Epub 2011 Jul 13. Neuromuscul Disord. 2012. PMID: 21689937 No abstract available.
Fetal acetylcholine receptor inactivation syndrome: A myopathy due to maternal antibodies.
Hacohen Y, Jacobson LW, Byrne S, Norwood F, Lall A, Robb S, Dilena R, Fumagalli M, Born AP, Clarke D, Lim M, Vincent A, Jungbluth H. Hacohen Y, et al. Among authors: norwood f. Neurol Neuroimmunol Neuroinflamm. 2014 Dec 23;2(1):e57. doi: 10.1212/NXI.0000000000000057. eCollection 2015 Feb. Neurol Neuroimmunol Neuroinflamm. 2014. PMID: 25566546 Free PMC article.
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