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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: menezes mm. Genes (Basel). 2022 Apr 26;13(5):760. doi: 10.3390/genes13050760. Genes (Basel). 2022. PMID: 35627144 Free PMC article.
Common recessive limb girdle muscular dystrophies differential diagnosis: why and how?
Cotta A, Carvalho E, da-Cunha-Júnior AL, Paim JF, Navarro MM, Valicek J, Menezes MM, Nunes SV, Xavier Neto R, Takata RI, Vargas AP. Cotta A, et al. Among authors: menezes mm. Arq Neuropsiquiatr. 2014 Sep;72(9):721-34. doi: 10.1590/0004-282x20140110. Arq Neuropsiquiatr. 2014. PMID: 25252238 Free article. Review.
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. Among authors: menezes mm. 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. Among authors: menezes mm. Arq Neuropsiquiatr. 2017 Nov;75(11):789-795. doi: 10.1590/0004-282X20170151. Arq Neuropsiquiatr. 2017. PMID: 29236822 Free article.