| 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 | 128 | 2012 |
| 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 | 82 | 2017 |
| 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 | 61 | 2004 |
| 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 | 57 | 2002 |
| 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 | 51 | 1995 |
| 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 | 42 | 2007 |
| 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 | 42 | 1998 |
| Detection and analysis of mitochondrial DNA deletions by whole genome PCR CH Tengan, CT Moraes Biochemical and molecular medicine 58 (1), 130-134, 1996 | 40 | 1996 |
| 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 | 39 | 1997 |
| 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 | 32 | 1993 |
| Doenças mitocondriais IE Nasseh, CH Tengan, BH Kiyomoto, AA Gabbai Revista Neurociências 9 (2), 60-69, 2001 | 27 | 2001 |
| 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 | 27 | 1997 |
| 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 | 21 | 1998 |
| 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 | 19 | 2012 |
| 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 | 19 | 2006 |
| 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 | 16 | 2008 |
| 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 | 16 | 2000 |
| 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 | 14 | 2002 |
| 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 | 13 | 2008 |
| The mutations m. 5628T> C and m. 8348A> G in single muscle fibers of a patient with chronic progressive external ophthalmoplegia J Gamba, BH Kiyomoto, ASB de Oliveira, AA Gabbai, B Schmidt, ... Journal of the neurological sciences 320 (1-2), 131-135, 2012 | 12 | 2012 |
