Publications by authors named "Bruno Augusto Telles"

3Publications

Neurodevelopmental regression, severe generalized dystonia, and metabolic acidosis caused by mutations.

Authors:
Vanessa Zanette Aurelio Reyes Mark Johnson Daniel do Valle Alan J Robinson Vaneisse Monteiro Bruno Augusto Telles Ricardo L R Souza Mara L S F Santos Cristiane Benincá Massimo Zeviani

Neurol Genet 2020 Dec 7;6(6):e521. Epub 2020 Oct 7.

Medical Research Council-Mitochondrial Biology Unit (A.R., M.J., A.J.R., C.B., M.Z.), University of Cambridge, United Kingdom; Department of Genetics (V.Z., R.L.R.S., C.B.), Federal University of Paraná-UFPR; and Neuropediatric Division (V.M., M.L.S.F.S., D.V., B.A.T.), Hospital Pequeno Príncipe, Curitiba, Brazil.

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December 2020

The importance of staged surgery for giant atypical central neurocytoma.

Authors:
Jennyfer Paulla Galdino Chaves Carlos Alberto Mattozo Bruno Augusto Telles Ana Paula Percicote Zeferino Jr Demartini Adriano Keijiro Maeda

Acta Neurol Belg 2020 Aug 28. Epub 2020 Aug 28.

Neurosurgery Department of Pequeno Príncipe Hospital, 1070 Desembargador Motta street, Água Verde, Curitiba-PR, 80250-060, Brazil.

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August 2020

Mutation in the MICOS subunit gene (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features.

Authors:
Cristiane Benincá Vanessa Zanette Michele Brischigliaro Mark Johnson Aurelio Reyes Daniel Almeida do Valle Alan J Robinson Andrea Degiorgi Anna Yeates Bruno Augusto Telles Julien Prudent Enrico Baruffini Mara Lucia S F Santos Ricardo Lehtonen R de Souza Erika Fernandez-Vizarra Alexander J Whitworth Massimo Zeviani

J Med Genet 2020 05 21. Epub 2020 May 21.

Medical Research Council, Mitochondrial Biology Unit, Cambridge, Cambridgeshire, UK

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May 2020