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

Year Number of Results
1989 2
1990 1
1991 3
1992 2
1993 5
1994 1
1995 3
1996 2
1997 1
1998 1
1999 4
2000 1
2001 1
2002 1
2003 1
2004 4
2005 1
2006 2
2007 1
2009 1
2010 1
2012 1
2013 1
2014 4
2017 1
2018 3
2020 3
2021 1
2022 1
2024 0

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53 results

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Page 1
Steroids in Duchenne dystrophy.
Zatz M, Pavanello RC. Zatz M, et al. Among authors: pavanello rc. Neuromuscul Disord. 2013 Nov;23(11):952-3. doi: 10.1016/j.nmd.2013.07.013. Epub 2013 Aug 13. Neuromuscul Disord. 2013. PMID: 24012246 No abstract available.
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: pavanello rcm. 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.
Development of a comprehensive noninvasive prenatal test.
Malcher C, Yamamoto GL, Burnham P, Ezquina SAM, Lourenço NCV, Balkassmi S, Antonio DSM, Hsia GSP, Gollop T, Pavanello RC, Lopes MA, Bakker E, Zatz M, Bertola D, Vlaminck I, Passos-Bueno MR. Malcher C, et al. Among authors: pavanello rc. Genet Mol Biol. 2018 Jul/Sept.;41(3):545-554. doi: 10.1590/1678-4685-GMB-2017-0177. Epub 2018 Jul 16. Genet Mol Biol. 2018. PMID: 30043834 Free PMC article.
Nemaline Myopathy in Brazilian Patients: Molecular and Clinical Characterization.
Gurgel-Giannetti J, Souza LS, Yamamoto GL, Belisario M, Lazar M, Campos W, Pavanello RCM, Zatz M, Reed U, Zanoteli E, Oliveira AB, Lehtokari VL, Casella EB, Machado-Costa MC, Wallgren-Pettersson C, Laing NG, Nigro V, Vainzof M. Gurgel-Giannetti J, et al. Among authors: pavanello rcm. Int J Mol Sci. 2022 Oct 9;23(19):11995. doi: 10.3390/ijms231911995. Int J Mol Sci. 2022. PMID: 36233295 Free PMC article.
Dysferlin protein analysis in limb-girdle muscular dystrophies.
Vainzof M, Anderson LV, McNally EM, Davis DB, Faulkner G, Valle G, Moreira ES, Pavanello RC, Passos-Bueno MR, Zatz M. Vainzof M, et al. Among authors: pavanello rc. J Mol Neurosci. 2001 Aug;17(1):71-80. doi: 10.1385/JMN:17:1:71. J Mol Neurosci. 2001. PMID: 11665864
Altered in vitro muscle differentiation in X-linked myopathy with excessive autophagy.
Fernandes SA, Almeida CF, Souza LS, Lazar M, Onofre-Oliveira P, Yamamoto GL, Nogueira L, Tasaki LY, Cardoso RR, Pavanello RCM, Silva HCA, Ferrari MFR, Bigot A, Mouly V, Vainzof M. Fernandes SA, et al. Among authors: pavanello rcm. Dis Model Mech. 2020 Jan 10;13(2):dmm041244. doi: 10.1242/dmm.041244. Dis Model Mech. 2020. PMID: 31826868 Free PMC article.
Manifesting carriers of X-linked myotubular myopathy: Genetic modifiers modulating the phenotype.
Souza LS, Almeida CF, Yamamoto GL, Pavanello RCM, Gurgel-Giannetti J, da Costa SS, Anequini IP, do Carmo SA, Wang JYT, Scliar MO, Castelli EC, Otto PA, Zanoteli E, Vainzof M. Souza LS, et al. Among authors: pavanello rcm. Neurol Genet. 2020 Sep 4;6(5):e513. doi: 10.1212/NXG.0000000000000513. eCollection 2020 Oct. Neurol Genet. 2020. PMID: 33062893 Free PMC article.
A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G).
Vieira NM, Naslavsky MS, Licinio L, Kok F, Schlesinger D, Vainzof M, Sanchez N, Kitajima JP, Gal L, Cavaçana N, Serafini PR, Chuartzman S, Vasquez C, Mimbacas A, Nigro V, Pavanello RC, Schuldiner M, Kunkel LM, Zatz M. Vieira NM, et al. Among authors: pavanello rc. Hum Mol Genet. 2014 Aug 1;23(15):4103-10. doi: 10.1093/hmg/ddu127. Epub 2014 Mar 18. Hum Mol Genet. 2014. PMID: 24647604
53 results