Leticia Nogueira Feitosa

Formação complementar

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Produções bibliográficas

• VASCONCELOS, FELIPE TADEU GALANTE ROCHA DE ; RIBEIRO JÚNIOR, ANTONIO FERNANDO ; SOUZA, BRANDOW WILLY ; ZOGBI, ISABELA DE AQUINO ; CARVALHO, LAURA MACHADO LARA ; FEITOSA, LETÍCIA NOGUEIRA ; SOUZA, LUCAS SANTOS ; SALDYS, NATHÁLIA GAGLIARDI ; FERRARI, MERARI DE FÁTIMA RAMIRES ; VAINZOF, MARIZ . Induced degeneration and regeneration in aged muscle reduce tubular aggregates but not muscle function. Frontiers in Neurology , v. 15, p. 1-9, 2024.

• COTTA, ANA ; SOUZA, LUCAS SANTOS ; CARVALHO, ELMANO ; FEITOSA, LETICIA NOGUEIRA ; CUNHA, ANTONIO ; NAVARRO, MONICA MACHADO ; VALICEK, JAQUELIN ; MENEZES, MIRIAM MELO ; NEVES, SIMONE VILELA NUNES ; XAVIER-NETO, RAFAEL ; VARGAS, ANTONIO PEDRO ; TAKATA, REINALDO ISSAO ; PAIM, JULIA FILARDI ; VAINZOF, MARIZ . Central Core Disease: Facial Weakness Differentiating Biallelic from Monoallelic Forms. Genes , v. 13, p. 760, 2022.

• LEÃO, LEONARDO G. ; SOUZA, L. S. ; FEITOSA, L. N. ; PAVANELLO, R. ; GURGEL-GIANNETTI, J. ; REED, U. C. ; OLIVEIRA, A. S. B. ; CUPERMAN, T. ; COTTA, ANA ; PAIM, JULIA F. ; ZATZ, M ; VAINZOF, M. . Dominant or recessive mutations in the RYR1 gene causing central core myopathy in Brazilian patients. Acta Myol , v. 39, p. 274-282, 2020.

• FERNANDES, STEPHANIE A. ; ALMEIDA, CAMILA F. ; SOUZA, LUCAS S. ; LAZAR, MONIZE ; ONOFRE-OLIVEIRA, PAULA ; YAMAMOTO, GUILHERME L. ; NOGUEIRA, LETÍCIA ; TASAKI, LETÍCIA Y. ; CARDOSO, RAFAELA R. ; PAVANELLO, RITA C. M. ; SILVA, HELGA C. A. ; FERRARI, MERARI F. R. ; BIGOT, ANNE ; MOULY, VINCENT ; VAINZOF, MARIZ . Altered in vitro muscle differentiation in X-linked myopathy with excessive autophagy (XMEA). Disease Models & Mechanisms , v. 13, p. dmm041244, 2019.

• COTTA, ANA ; PAIM, JULIA F. ; PAVANELLO, RITA DE C. M. ; NOGUEIRA, LETICIA ; LEÃO, LEONARDO G. ; XAVIER-NETO, RAFAEL ; NAVARRO, MONICA M. ; CARVALHO, ELMANO ; VALICEK, JAQUELIN ; SILVEIRA, ENI B. ; TAKATA, REINALDO I. ; VAINZOF, MARIZ . Central core myopathy with autophagy. MUSCLE & NERVE , v. 56, p. E8-E9, 2017.

• VAINZOF, MARIZ ; FEITOSA, LETICIA ; CANOVAS, MARTA ; AYUB-GUERRIERI, DANIELLE ; PAVANELLO, RITA DE CÁSSIA M. ; ZATZ, MAYANA . Concordant utrophin upregulation in phenotypically discordant DMD/BMD brothers. Neuromuscular Disorders , v. 24, p. (11):986-9., 2016.

• ZATZ, M. ; PAVANELLO, R.C.M. ; LAZAR, M. ; YAMAMOTO, G.L. ; LOURENÇO, N.C.V. ; CERQUEIRA, A. ; NOGUEIRA, L. ; VAINZOF, M. . Milder course in Duchenne patients with nonsense mutations and no muscle dystrophin. Neuromuscular Disorders , v. 24, p. 986, 2014.

• VAINZOF., M. ; PELLAES, L. N. F. ; CANOVAS, M. ; PAVANELLO, R. ; ZATZ, M. . Mild course in atypical Duchenne muscular dystrophy patients is not caused by utrophin overexpression. In: 20th International Congress of the Word Muscle Society, 2015, Brighton. Livro de Resumos do Evento, 2015.

• VAINZOF., M. ; LAMonize LazarZAR, M. ; Guilherme Yamamoto ; ALMEIDA, C. F. ; ONOFRE-OLIVIEIRA, P. C. ; FEITOSA, L. N. ; YAMAMOTO, L. U. ; ZATZ, M ; PAVANELLO, R. C. M ; SILVA, H. C. . X-linked myopathy with excessive autophagy (XMEA): NGS identifies a new in/del in the cric splicing region of the VMA21 gene. In: 13th International Congress on Neuromuscular Diseases, 2014, Nice. Journal of Neuromuscular Diseases, 2014.

• VAINZOF., M. ; LAMonize LazarZAR, M. ; Guilherme Yamamoto ; ALMEIDA, C. F. ; ONOFRE-OLIVIEIRA, P. C. ; FEITOSA, L. N. ; YAMAMOTO, L. U. ; ZATZ, M ; SILVA, H. C. . A new in/del in the critical splicing region of the VMA21 gene causing X-linked myopathy with excessive autophagy (XMEA). In: 19th International Congress of The World Muscle Society, 2014, Berlim. Livro de Resumos do Evento, 2014.

• ZATZ, M. ; PAVANELLO, R. ; LAMonize LazarZAR, M. ; LOURENCO, N. C. V. ; CERQUEIRA, A. ; FEITOSA, L. N. ; VAINZOF., M. . Milder course in patients with nonsense mutations and no muscle dystrophin. In: Meeting of the ASHG, 2013, Boston. Livro de Resumos do Evento, 2013.

• ZATZ, M. ; PAVANELLO, RITA DE CÁSSIA M. ; VIEIRA, N. M. ; GOMES, J. P. ; ASSONI, A. F. ; ANEQUINI, I. P. ; FEITOSA, L. N. ; CANOVAS, M. ; PELLATTI, M. ; VAINZOF., M. . Duchenne clinically discordant brothers: A ?Ringo-like? phenotype in humans?. In: 17th International World Muscle Society Congress, 2012, Perth. Livro de Resumos do Evento, 2012.

• VAINZOF., M. ; PAVANELLO, R. C. M ; FEITOSA, L. N. ; YAMAMOTO, L. U. ; ZATZ, M. . Sarcoglicanopatias. In: XXV Congresso Brasileiro de Neurologia, 2012, Goiânia. Livro de Resumos do Evento, 2012.

• LANZOTTI, A. A. ; ONOFRE-OLIVIEIRA, P. C. ; MARTINS., P. C. M. ; BACH., A. B. M. ; FEITOSA, L. N. ; VAINZOF., M. . The mdx/SJL mouse: a new double mutant model for neuromuscular disorders with mutations in the dystrophin and dysferlin genes. In: 16th International Congress of the World Muscle Society, 2011, Almancil, Alarve. Livro de Resumos do Evento., 2011.

• ONOFRE-OLIVIEIRA, P. C. ; MARTINS., P. C. M. ; LANZOTTI, A. A. ; ALMEIDA, C. F. ; FEITOSA, L. N. ; Calyjur, P ; Ayub-Guerrieri, D ; VAINZOF., M. . Myogenic Potential of Murine Mesenchymal Stem Cells for Therapy in Progressive Muscular Dystrophies. In: ISSCR 9th Annual Meeting, 2011, Toronto. Toronto. ISSCR - Poster Abstracts, 2011.