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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1981 1
1982 1
1984 4
1985 4
1987 3
1988 2
1989 1
1990 1
1991 3
1992 3
1993 4
1994 7
1995 13
1996 5
1997 15
1998 13
1999 15
2000 13
2001 13
2002 15
2003 14
2004 15
2005 11
2006 8
2007 11
2008 11
2009 9
2010 17
2011 19
2012 11
2013 19
2014 16
2015 15
2016 13
2017 9
2018 9
2019 8
2020 3
2021 6
2022 3
2023 2
2024 3

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335 results

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Page 1
Nemaline myopathies: a current view.
Sewry CA, Laitila JM, Wallgren-Pettersson C. Sewry CA, et al. J Muscle Res Cell Motil. 2019 Jun;40(2):111-126. doi: 10.1007/s10974-019-09519-9. Epub 2019 Jun 21. J Muscle Res Cell Motil. 2019. PMID: 31228046 Free PMC article. Review.
Core myopathies.
Jungbluth H, Sewry CA, Muntoni F. Jungbluth H, et al. Among authors: sewry ca. Semin Pediatr Neurol. 2011 Dec;18(4):239-49. doi: 10.1016/j.spen.2011.10.005. Semin Pediatr Neurol. 2011. PMID: 22172419 Review.
Nemaline myopathies.
Wallgren-Pettersson C, Sewry CA, Nowak KJ, Laing NG. Wallgren-Pettersson C, et al. Among authors: sewry ca. Semin Pediatr Neurol. 2011 Dec;18(4):230-8. doi: 10.1016/j.spen.2011.10.004. Semin Pediatr Neurol. 2011. PMID: 22172418 Review.
Congenital muscular dystrophies.
Mercuri E, Sewry C, Brown SC, Muntoni F. Mercuri E, et al. Among authors: sewry c. Semin Pediatr Neurol. 2002 Jun;9(2):120-31. doi: 10.1053/spen.2002.33802. Semin Pediatr Neurol. 2002. PMID: 12138996 Review.
Congenital muscular dystrophies in the UK population: Clinical and molecular spectrum of a large cohort diagnosed over a 12-year period.
Sframeli M, Sarkozy A, Bertoli M, Astrea G, Hudson J, Scoto M, Mein R, Yau M, Phadke R, Feng L, Sewry C, Fen ANS, Longman C, McCullagh G, Straub V, Robb S, Manzur A, Bushby K, Muntoni F. Sframeli M, et al. Among authors: sewry c. Neuromuscul Disord. 2017 Sep;27(9):793-803. doi: 10.1016/j.nmd.2017.06.008. Epub 2017 Jun 16. Neuromuscul Disord. 2017. PMID: 28688748
Myopathology in congenital myopathies.
Sewry CA, Wallgren-Pettersson C. Sewry CA, et al. Neuropathol Appl Neurobiol. 2017 Feb;43(1):5-23. doi: 10.1111/nan.12369. Neuropathol Appl Neurobiol. 2017. PMID: 27976420 Review.
Congenital myopathies.
Sewry CA, Jimenez-Mallebrera C, Muntoni F. Sewry CA, et al. Curr Opin Neurol. 2008 Oct;21(5):569-75. doi: 10.1097/WCO.0b013e32830f93c7. Curr Opin Neurol. 2008. PMID: 18769251 Review.
Non-sarcolemmal muscular dystrophies.
Brown SC, Muntoni F, Sewry CA. Brown SC, et al. Among authors: sewry ca. 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.
Pathological defects in congenital myopathies.
Sewry CA. Sewry CA. J Muscle Res Cell Motil. 2008;29(6-8):231-8. doi: 10.1007/s10974-008-9155-8. Epub 2008 Dec 30. J Muscle Res Cell Motil. 2008. PMID: 19115049 Review.
Loss of Function of the Cytoplasmic Fe-S Assembly Protein CIAO1 Causes a Neuromuscular Disorder with Compromise of Nucleocytoplasmic Fe-S Enzymes.
Maio N, Orbach R, Zaharieva I, Töpf A, Donkervoort S, Munot P, Mueller J, Willis T, Verma S, Peric S, Krishnakumar D, Sudhakar S, Foley AR, Silverstein S, Douglas G, Pais L, DiTroia S, Grunseich C, Hu Y, Sewry C, Sarkozy A, Straub V, Muntoni F, Rouault T, Bönnemann CG. Maio N, et al. Among authors: sewry c. medRxiv [Preprint]. 2023 Dec 20:2023.12.20.23300170. doi: 10.1101/2023.12.20.23300170. medRxiv. 2023. Update in: J Clin Invest. 2024 Jun 17;134(12):e179559. doi: 10.1172/JCI179559 PMID: 38196629 Free PMC article. Updated. Preprint.
335 results