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

Year Number of Results
1982 1
1988 2
1989 2
1990 3
1992 2
1993 2
1994 2
1995 4
1996 2
1997 5
1998 4
1999 4
2000 4
2001 6
2002 8
2003 5
2004 7
2005 2
2006 5
2007 4
2008 3
2009 10
2010 2
2011 6
2012 7
2013 7
2014 6
2015 6
2016 3
2017 2
2018 11
2019 8
2020 4
2021 4
2022 4
2023 4
2024 3

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148 results

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Page 1
Recent advances in nemaline myopathy.
Laitila J, Wallgren-Pettersson C. Laitila J, et al. Among authors: wallgren pettersson c. Neuromuscul Disord. 2021 Oct;31(10):955-967. doi: 10.1016/j.nmd.2021.07.012. Epub 2021 Jul 24. Neuromuscul Disord. 2021. PMID: 34561123 Free article. Review.
Nemaline myopathies: a current view.
Sewry CA, Laitila JM, Wallgren-Pettersson C. Sewry CA, et al. Among authors: wallgren pettersson c. 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.
Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness.
Töpf A, Johnson K, Bates A, Phillips L, Chao KR, England EM, Laricchia KM, Mullen T, Valkanas E, Xu L, Bertoli M, Blain A, Casasús AB, Duff J, Mroczek M, Specht S, Lek M, Ensini M, MacArthur DG; MYO-SEQ consortium; Straub V. Töpf A, et al. Genet Med. 2020 Sep;22(9):1478-1488. doi: 10.1038/s41436-020-0840-3. Epub 2020 Jun 11. Genet Med. 2020. PMID: 32528171 Free PMC article.
Mutation update: the spectra of nebulin variants and associated myopathies.
Lehtokari VL, Kiiski K, Sandaradura SA, Laporte J, Repo P, Frey JA, Donner K, Marttila M, Saunders C, Barth PG, den Dunnen JT, Beggs AH, Clarke NF, North KN, Laing NG, Romero NB, Winder TL, Pelin K, Wallgren-Pettersson C. Lehtokari VL, et al. Among authors: wallgren pettersson c. Hum Mutat. 2014 Dec;35(12):1418-26. doi: 10.1002/humu.22693. Hum Mutat. 2014. PMID: 25205138 Free PMC article.
Nemaline myopathies.
Wallgren-Pettersson C, Sewry CA, Nowak KJ, Laing NG. Wallgren-Pettersson C, et al. Semin Pediatr Neurol. 2011 Dec;18(4):230-8. doi: 10.1016/j.spen.2011.10.004. Semin Pediatr Neurol. 2011. PMID: 22172418 Review.
Ethics in genetic counselling.
Clarke AJ, Wallgren-Pettersson C. Clarke AJ, et al. Among authors: wallgren pettersson c. J Community Genet. 2019 Jan;10(1):3-33. doi: 10.1007/s12687-018-0371-7. Epub 2018 Jun 14. J Community Genet. 2019. PMID: 29949066 Free PMC article. Review.
Myopathology in congenital myopathies.
Sewry CA, Wallgren-Pettersson C. Sewry CA, et al. Among authors: wallgren pettersson c. Neuropathol Appl Neurobiol. 2017 Feb;43(1):5-23. doi: 10.1111/nan.12369. Neuropathol Appl Neurobiol. 2017. PMID: 27976420 Review.
Update on the Genetics of Congenital Myopathies.
Pelin K, Wallgren-Pettersson C. Pelin K, et al. Among authors: wallgren pettersson c. Semin Pediatr Neurol. 2019 Apr;29:12-22. doi: 10.1016/j.spen.2019.01.005. Epub 2019 Jan 17. Semin Pediatr Neurol. 2019. PMID: 31060721 Review.
Centronuclear (myotubular) myopathy.
Jungbluth H, Wallgren-Pettersson C, Laporte J. Jungbluth H, et al. Among authors: wallgren pettersson c. Orphanet J Rare Dis. 2008 Sep 25;3:26. doi: 10.1186/1750-1172-3-26. Orphanet J Rare Dis. 2008. PMID: 18817572 Free PMC article. Review.
Congenital myopathies.
Wallgren-Pettersson C. Wallgren-Pettersson C. Eur J Paediatr Neurol. 2005;9(1):27-8. doi: 10.1016/j.ejpn.2004.10.007. Epub 2004 Dec 13. Eur J Paediatr Neurol. 2005. PMID: 15701564 No abstract available.
148 results