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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 3

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189 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.
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
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.
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.
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.
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.
A normal life without muscle dystrophin.
Zatz M, Vieira NM, Zucconi E, Pelatti M, Gomes J, Vainzof M, Martins-Bach AB, Garcia Otaduy MC, Bento dos Santos G, Amaro E Jr, Landini V, Andrade T. Zatz M, et al. Among authors: vainzof m. Neuromuscul Disord. 2015 May;25(5):371-4. doi: 10.1016/j.nmd.2015.02.007. Epub 2015 Feb 24. Neuromuscul Disord. 2015. PMID: 25770920
Idiopathic hyperCKemia and malignant hyperthermia susceptibility.
Santos JM, Andrade PV, Galleni L, Vainzof M, Sobreira CFR, Schmidt B, Oliveira ASB, Amaral JLG, Silva HCA. Santos JM, et al. Among authors: vainzof m. Can J Anaesth. 2017 Dec;64(12):1202-1210. doi: 10.1007/s12630-017-0978-x. Epub 2017 Sep 26. Can J Anaesth. 2017. PMID: 28952030 English.
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.
Central Core Disease: Facial Weakness Differentiating Biallelic from Monoallelic Forms.
Cotta A, Souza LS, Carvalho E, Feitosa LN, Cunha A Jr, Navarro MM, Valicek J, Menezes MM, Neves SVN, Xavier-Neto R, Vargas AP, Takata RI, Paim JF, Vainzof M. Cotta A, et al. Among authors: vainzof m. Genes (Basel). 2022 Apr 26;13(5):760. doi: 10.3390/genes13050760. Genes (Basel). 2022. PMID: 35627144 Free PMC article.
189 results