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Page 1
Muscle Biopsy Reporting.
Cotta A, Paim JF. Cotta A, et al. Arch Pathol Lab Med. 2016 Sep;140(9):879. doi: 10.5858/arpa.2016-0070-LE. Arch Pathol Lab Med. 2016. PMID: 27575261 Free article. 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. 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.
Phenotypic Variability of Dystrophinopathy Symptomatic Female Carriers.
Cotta A, Paim JF, Carvalho E, Navarro MM, Valicek J, da-Cunha-Junior AL, Menezes MM, Nunes SV, Xavier-Neto R, da Silveira EB, Costa-E-Silva C, Takata RI, Vargas AP. Cotta A, et al. Can J Neurol Sci. 2017 May;44(3):304-310. doi: 10.1017/cjn.2016.448. Epub 2017 Feb 9. Can J Neurol Sci. 2017. PMID: 28181471
LMNA-Related Muscular Dystrophy with Clinical Intrafamilial Variability.
Cotta A, Paim JF, Carvalho E, Valicek J, da Cunha Junior AL, Navarro MM, Vargas AP, Lima MI, de Almeida CF, Takata RI, Vainzof M. Cotta A, et al. J Mol Neurosci. 2019 Dec;69(4):623-627. doi: 10.1007/s12031-019-01390-0. Epub 2019 Aug 13. J Mol Neurosci. 2019. PMID: 31410651
Metabolic shift underlies recovery in reversible infantile respiratory chain deficiency.
Hathazi D, Griffin H, Jennings MJ, Giunta M, Powell C, Pearce SF, Munro B, Wei W, Boczonadi V, Poulton J, Pyle A, Calabrese C, Gomez-Duran A, Schara U, Pitceathly RDS, Hanna MG, Joost K, Cotta A, Paim JF, Navarro MM, Duff J, Mattman A, Chapman K, Servidei S, Della Marina A, Uusimaa J, Roos A, Mootha V, Hirano M, Tulinius M, Giri M, Hoffmann EP, Lochmüller H, DiMauro S, Minczuk M, Chinnery PF, Müller JS, Horvath R. Hathazi D, et al. Among authors: cotta a. EMBO J. 2020 Dec 1;39(23):e105364. doi: 10.15252/embj.2020105364. Epub 2020 Oct 31. EMBO J. 2020. PMID: 33128823 Free PMC article.
Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy.
Winckler PB, da Silva AMS, Coimbra-Neto AR, Carvalho E, Cavalcanti EBU, Sobreira CFR, Marrone CD, Machado-Costa MC, Carvalho AAS, Feio RHF, Rodrigues CL, Gonçalves MVM, Tenório RB, Mendonça RH, Cotta A, Paim JFO, Costa E Silva C, de Aquino Cruz C, Bená MI, Betancur DFA, El Husny AS, de Souza ICN, Duarte RCB, Reed UC, Chaves MLF, Zanoteli E, França MC Jr, Saute JA. Winckler PB, et al. Among authors: cotta a. Clin Genet. 2019 Oct;96(4):341-353. doi: 10.1111/cge.13597. Epub 2019 Jul 15. Clin Genet. 2019. PMID: 31268554
Limb Length Discrepancy on an 11-Month-Old Boy with Osteoid Osteoma.
Cotta A, de Castro RCR, Paim JF, Fiuza LS, Lyra MHF. Cotta A, et al. Rev Bras Ortop (Sao Paulo). 2019 Apr;54(2):210-213. doi: 10.1016/j.rboe.2017.11.001. Epub 2019 Apr 22. Rev Bras Ortop (Sao Paulo). 2019. PMID: 31363270 Free PMC article.
Clinical, imaging, morphologic, and molecular features of X-linked VMA21-related myopathy in two unrelated Brazilian families.
Cotta A, Carvalho E, da-Cunha-Junior AL, Navarro MM, Menezes MM, Paim JF, Valicek J, Lima MI, Velloso-Filho R, Freire-Lyra MH, Takata RI, Inoue M, Okubo M, Iida A, Nishino I. Cotta A, et al. J Neurol Sci. 2020 Aug 15;415:116977. doi: 10.1016/j.jns.2020.116977. Epub 2020 Jun 5. J Neurol Sci. 2020. PMID: 32535249 No abstract available.
19 results