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Celia Harumi Tengan
Celia Harumi Tengan
Universidade Federal de São Paulo, Escola Paulista de Medicina
E-mail confirmado em unifesp.br
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Nitric oxide in skeletal muscle: role on mitochondrial biogenesis and function
CH Tengan, GS Rodrigues, RO Godinho
International journal of molecular sciences 13 (12), 17160-17184, 2012
1262012
NO control of mitochondrial function in normal and transformed cells
CH Tengan, CT Moraes
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1858 (8), 573-581, 2017
802017
The exercise test as a monitor of disease status in hypokalaemic periodic paralysis
CH Tengan, AC Antunes, AA Gabbai, GM Manzano
Journal of Neurology, Neurosurgery & Psychiatry 75 (3), 497-499, 2004
612004
Mutations linked to familial hypokalaemic periodic paralysis in the calcium channel α1 subunit gene (Cav1·1) are not associated with thyrotoxic hypokalaemic …
MR Dias da Silva, JM Cerutti, CH Tengan, GK Furuzawa, TCA Vieira, ...
Clinical endocrinology 56 (3), 367-375, 2002
572002
Mutations linked to familial hypokalaemic periodic paralysis in the calcium channel α1 subunit gene (Cav1·1) are not associated with thyrotoxic hypokalaemic …
MR Dias da Silva, JM Cerutti, CH Tengan, GK Furuzawa, TCA Vieira, ...
Clinical endocrinology 56 (3), 367-375, 2002
572002
Phenotype–genotype correlations in skeletal muscle of patients with mtDNA deletions
CT Moraes, M Sciacco, E Ricci, CH Tengan, H Hao, E Bonilla, EA Schon, ...
Muscle & Nerve: Official Journal of the American Association of …, 1995
511995
The role of nitric oxide in muscle fibers with oxidative phosphorylation defects
CH Tengan, BH Kiyomoto, RO Godinho, J Gamba, AC Neves, B Schmidt, ...
Biochemical and biophysical research communications 359 (3), 771-777, 2007
422007
Mitochondrial encephalomyopathy and hypoparathyrodism associated with a duplication and a deletion of mitochondrial deoxyribonucleic acid
CH Tengan, BH Kiyomoto, MS Rocha, VLS Tavares, AA Gabbai, ...
The Journal of Clinical Endocrinology & Metabolism 83 (1), 125-129, 1998
421998
Detection and analysis of mitochondrial DNA deletions by whole genome PCR
CH Tengan, CT Moraes
Biochemical and molecular medicine 58 (1), 130-134, 1996
401996
Oxidative phosphorylation dysfunction does not increase the rate of accumulation of age-related mtDNA deletions in skeletal muscle
CH Tengan, AA Gabbai, S Shanske, M Zeviani, CT Moraes
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 379 (1 …, 1997
391997
Isolated and painless infraspinatus atrophy in top-level volleyball players: report of two cases and review of the literature
CH Tengan, ASB Oliveira, BH Kiymoto, MPA Morita, JL Medeiros, ...
Arquivos de Neuro-Psiquiatria 51, 125-129, 1993
321993
Doenças mitocondriais
IE Nasseh, CH Tengan, BH Kiyomoto, AA Gabbai
Revista Neurociências 9 (2), 60-69, 2001
272001
Mitochondrial DNA defects in Brazilian patients with chronic progressive external ophthalmoplegia
BH Kiyomoto, CH Tengan, CT Moraes, ASB Oliveira, AA Gabbai
Journal of the neurological sciences 152 (2), 160-165, 1997
271997
Duplication and triplication with staggered breakpoints in human mitochondrial DNA
CH Tengan, CT Moraes
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1406 (1), 73-80, 1998
211998
Nitric oxide synthesis is increased in cybrid cells with m. 3243A> G mutation
J Gamba, LT Gamba, GS Rodrigues, BH Kiyomoto, CT Moraes, ...
International journal of molecular sciences 14 (1), 394-410, 2012
192012
Investigation of mitochondrial involvement in the experimental model of epilepsy induced by pilocarpine
IE Nasseh, D Amado, EA Cavalheiro, M da Graça Naffah-Mazzacoratti, ...
Epilepsy research 68 (3), 229-239, 2006
192006
Effects of short-term zidovudine exposure on mitochondrial DNA content and succinate dehydrogenase activity of rat skeletal muscle cells
BH Kiyomoto, CH Tengan, RO Godinho
Journal of the neurological sciences 268 (1-2), 33-39, 2008
162008
A novel myopathy-associated mitochondrial DNA mutation altering the conserved size of the tRNAGln anticodon loop
R Dey, CH Tengan, MPA Morita, BH Kiyomoto, CT Moraes
Neuromuscular Disorders 10 (7), 488-492, 2000
152000
Frequency of duplications in the D-loop in patients with mitochondrial DNA deletions
CH Tengan, C Ferreiro-Barros, M Cardeal, MAT Fireman, ASB Oliveira, ...
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1588 (1), 65-70, 2002
142002
Neonatal mitochondrial encephaloneuromyopathy due to a defect of mitochondrial protein synthesis
CC Ferreiro-Barros, CH Tengan, MH Barros, L Palenzuela, C Kanki, ...
Journal of the neurological sciences 275 (1-2), 128-132, 2008
132008
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