Browsing by Author Tengan, Celia Harumi [UNIFESP]

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Showing results 1 to 14 of 14
Issue DateTitleAuthor(s)
1-Apr-2013Complex I spectrophotometric assay in cultured cells: Detailed analysis of key factorsOliveira, Katia Klug [UNIFESP]; Kiyomoto, Beatriz Hitomi [UNIFESP]; Rodrigues, Andresa De Santi [UNIFESP]; Tengan, Celia Harumi [UNIFESP]; Universidade Federal de São Paulo (UNIFESP)
1997Deleções do DNA mitocondrial no envelhecimento: efeito da disfunção na fosforilação oxidativaGabbai, Alberto Alain [UNIFESP]; Tengan, Celia Harumi [UNIFESP]
19-Dec-2018Estudo Dos Efeitos Da Suplementação De L-Arginina Sobre A Função E Conteúdo Mitocondrial Em Cultura De Células Com Deficiência MitocondrialTengan, Celia Harumi [UNIFESP]; Barros, Camila Dantas Dos Santos [UNIFESP]; Universidade Federal de São Paulo (UNIFESP)
1-Mar-2004The exercise test as a monitor of disease status in hypokalaemic periodic paralysisTengan, Celia Harumi [UNIFESP]; Antunes, A. C. [UNIFESP]; Gabbai, Alberto Alain [UNIFESP]; Manzano, Gilberto M. [UNIFESP]; Universidade Federal de São Paulo (UNIFESP)
2005A expressão da proteína mitocondrial ci-39kda na identificação de doenças mitocondriais associadas a defeitos do complexo ITengan, Celia Harumi [UNIFESP]; Rodrigues, Andresa De Santi [UNIFESP]; Universidade Federal de São Paulo (UNIFESP)
1-Apr-2006Frequency of dystrophic muscle abnormalities in chronic progressive external ophthalmoplegia: analysis of 86 patientsKiyomoto, Beatriz Hitomi [UNIFESP]; Tengan, Celia Harumi [UNIFESP]; Costa, C. K. [UNIFESP]; Oliveira, A. S. [UNIFESP]; Schmidt, B.; Gabbai, Alberto Alain [UNIFESP]; Universidade Federal de São Paulo (UNIFESP)
1-Mar-2002Mutations linked to familial hypokalaemic periodic paralysis in the calcium channel alpha 1 subunit gene (Ca(v)1 center dot 1) are not associated with thyrotoxic hypokalaemic periodic paralysisSilva, Magnus R Dias da [UNIFESP]; Cerutti, Janete Maria [UNIFESP]; Tengan, Celia Harumi [UNIFESP]; Furuzawa, Gilberto Koiti [UNIFESP]; Vieira, Teresa C. Alfinito [UNIFESP]; Gabbai, Alberto Alain [UNIFESP]; Maciel, Rui Monteiro de Barros [UNIFESP]; Universidade Federal de São Paulo (UNIFESP)
15-Sep-2012The mutations m.5628T > C and m18348A > G in single muscle fibers of a patient with chronic progressive external ophthalmoplegiaGamba, Juliana [UNIFESP]; Kiyomoto, Beatriz Hitomi [UNIFESP]; Oliveira, Acary Souza Bulle [UNIFESP]; Gabbai, Alberto Alain [UNIFESP]; Schmidt, Beny [UNIFESP]; Tengan, Celia Harumi [UNIFESP]; Universidade Federal de São Paulo (UNIFESP)
15-Dec-2008Neonatal mitochondrial encephaloneuromyopathy due to a defect of mitochondrial protein synthesisFerreiro-Barros, Claudia Cristina [UNIFESP]; Tengan, Celia Harumi [UNIFESP]; Barros, Mario Henrique de; Palenzuela, Lluis; Kanki, Chisaka; Quinzii, Catarina; Lou, Johanna; El Gharaby, Nader; Shokr, Aly; De Vivo, Darryl C.; DiMauro, Salvatore; Hirano, Michio; Columbia Univ; Universidade Federal de São Paulo (UNIFESP); Universidade de São Paulo (USP); Bugshan Gen Hosp
1-Dec-2012Nitric Oxide in Skeletal Muscle: Role on Mitochondrial Biogenesis and FunctionTengan, Celia Harumi [UNIFESP]; Rodrigues, Gabriela Silva [UNIFESP]; Godinho, Rosely Oliveira [UNIFESP]; Universidade Federal de São Paulo (UNIFESP)
1-Jan-2013Nitric Oxide Synthesis Is Increased in Cybrid Cells with m.3243A > G MutationGamba, Juliana [UNIFESP]; Gamba, Luana Tesser [UNIFESP]; Rodrigues, Gabriela S. [UNIFESP]; Kiyomoto, Beatriz Hitomi [UNIFESP]; Moraes, Carlos T.; Tengan, Celia Harumi [UNIFESP]; Universidade Federal de São Paulo (UNIFESP); Univ Miami
1993Paralisia periódica: estudo de vinte pacientesGabbai, Alberto Alain [UNIFESP]; Tengan, Celia Harumi [UNIFESP]
15-Jan-2008Progressive myopathy with a combined respiratory chain defect including Complex IIRodrigues, Andresa De Santi [UNIFESP]; Kiyomoto, Beatriz Hitomi [UNIFESP]; Oliveira, Acary Souza Bulle [UNIFESP]; Gabbai, Alberto Alain [UNIFESP]; Schmidt, Beny [UNIFESP]; Tengan, Celia Harumi [UNIFESP]; Universidade Federal de São Paulo (UNIFESP)
1-Jan-2006Stem cell transplantation is feasible in children with Pearson's syndrome and may change the fatal history of this mitochondrial disorder.Gordan, Letícia Navarro [UNIFESP]; Pereira, L. M.; Ginani, V. C.; Gouveia, R. V.; Lee, M. d.; Zeccin, V. G.; Petrilli, Antonio Sergio [UNIFESP]; Tengan, Celia Harumi [UNIFESP]; Seber, Adriana [UNIFESP]; Universidade Federal de São Paulo (UNIFESP)