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29 results

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Page 1
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.
Muscle phenotypic variability in limb girdle muscular dystrophy 2 G.
Paim JF, Cotta A, Vargas AP, Navarro MM, Valicek J, Carvalho E, da-Cunha AL Jr, Plentz E, Braz SV, Takata RI, Almeida CF, Vainzof M. Paim JF, et al. Among authors: cotta a. J Mol Neurosci. 2013 Jun;50(2):339-44. doi: 10.1007/s12031-013-9987-6. Epub 2013 Mar 12. J Mol Neurosci. 2013. PMID: 23479141
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.
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
The relative frequency of common neuromuscular diagnoses in a reference center.
Cotta A, Paim JF, Carvalho E, da-Cunha-Júnior AL, Navarro MM, Valicek J, Menezes MM, Nunes SV, Xavier-Neto R, Baptista S Junior, Lima LR, Takata RI, Vargas AP. Cotta A, et al. Arq Neuropsiquiatr. 2017 Nov;75(11):789-795. doi: 10.1590/0004-282X20170151. Arq Neuropsiquiatr. 2017. PMID: 29236822 Free 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.
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
29 results