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

Year Number of Results
1978 1
1985 2
1987 1
1988 2
1989 2
1990 1
1991 12
1992 5
1993 11
1994 3
1995 8
1996 9
1997 5
1998 6
1999 4
2000 7
2001 4
2002 4
2003 10
2004 3
2005 2
2006 3
2007 4
2008 5
2009 5
2010 4
2011 3
2012 8
2013 8
2014 8
2015 2
2016 7
2017 6
2018 3
2019 4
2020 5
2021 6
2022 6
2023 3
2024 1

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187 results

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Page 1
Sarcoglycanopathies: an update.
Vainzof M, Souza LS, Gurgel-Giannetti J, Zatz M. Vainzof M, et al. Neuromuscul Disord. 2021 Oct;31(10):1021-1027. doi: 10.1016/j.nmd.2021.07.014. Epub 2021 Jul 28. Neuromuscul Disord. 2021. PMID: 34404573 Review.
Approach to the diagnosis of congenital myopathies.
North KN, Wang CH, Clarke N, Jungbluth H, Vainzof M, Dowling JJ, Amburgey K, Quijano-Roy S, Beggs AH, Sewry C, Laing NG, Bönnemann CG; International Standard of Care Committee for Congenital Myopathies. North KN, et al. Among authors: vainzof m. Neuromuscul Disord. 2014 Feb;24(2):97-116. doi: 10.1016/j.nmd.2013.11.003. Epub 2013 Nov 18. Neuromuscul Disord. 2014. PMID: 24456932 Free PMC article.
Neurocognitive Impairment in mdx Mice.
Comim CM, Ventura L, Freiberger V, Dias P, Bragagnolo D, Dutra ML, Amaral RA, Camargo-Fagundes ALS, Reis PA, Castro-Faria-Neto HC, Vainzof M, Rosa MI. Comim CM, et al. Among authors: vainzof m. Mol Neurobiol. 2019 Nov;56(11):7608-7616. doi: 10.1007/s12035-019-1573-7. Epub 2019 May 10. Mol Neurobiol. 2019. PMID: 31077034
Protein defects in neuromuscular diseases.
Vainzof M, Zatz M. Vainzof M, et al. Braz J Med Biol Res. 2003 May;36(5):543-55. doi: 10.1590/s0100-879x2003000500001. Epub 2003 Apr 22. Braz J Med Biol Res. 2003. PMID: 12715073 Free article. Review.
Animal models for genetic neuromuscular diseases.
Vainzof M, Ayub-Guerrieri D, Onofre PC, Martins PC, Lopes VF, Zilberztajn D, Maia LS, Sell K, Yamamoto LU. Vainzof M, et al. J Mol Neurosci. 2008 Mar;34(3):241-8. doi: 10.1007/s12031-007-9023-9. Epub 2008 Jan 18. J Mol Neurosci. 2008. PMID: 18202836 Review.
Muscle Satellite Cells: Exploring the Basic Biology to Rule Them.
Almeida CF, Fernandes SA, Ribeiro Junior AF, Keith Okamoto O, Vainzof M. Almeida CF, et al. Among authors: vainzof m. Stem Cells Int. 2016;2016:1078686. doi: 10.1155/2016/1078686. Epub 2016 Mar 3. Stem Cells Int. 2016. PMID: 27042182 Free PMC article. Review.
Renewed avenues through exercise muscle contractility and inflammatory status.
Zanchi NE, Almeida FN, Lira FS, Rosa Neto JC, Nicastro H, da Luz CR, de Siqueira Filho MA, Felitti V, Vainzof M, Seelaender M, Poortmans JR, Lancha AH Jr. Zanchi NE, et al. Among authors: vainzof m. ScientificWorldJournal. 2012;2012:584205. doi: 10.1100/2012/584205. Epub 2012 May 3. ScientificWorldJournal. 2012. PMID: 22629149 Free PMC article. Review.
Central core myopathy with autophagy.
Cotta A, Paim JF, Pavanello RCM, Nogueira L, Leão LG, Xavier-Neto R, Navarro MM, Carvalho E, Valicek J, Silveira EB, Takata RI, Vainzof M. Cotta A, et al. Among authors: vainzof m. Muscle Nerve. 2017 Aug;56(2):E8-E9. doi: 10.1002/mus.25594. Epub 2017 Mar 21. Muscle Nerve. 2017. PMID: 28164363 No abstract available.
The 10 autosomal recessive limb-girdle muscular dystrophies.
Zatz M, de Paula F, Starling A, Vainzof M. Zatz M, et al. Among authors: vainzof m. Neuromuscul Disord. 2003 Sep;13(7-8):532-44. doi: 10.1016/s0960-8966(03)00100-7. Neuromuscul Disord. 2003. PMID: 12921790 Review.
187 results