C. Tengan

发表

Impaired Ganglion Cell Function Objectively Assessed by the Photopic Negative Response in Affected and Asymptomatic Members From Brazilian Families With Leber's Hereditary Optic Neuropathy

V. Carelli, A. Sadun, R. Karanjia, 2021, Frontiers in Neurology.

A novel myopathy-associated mitochondrial DNA mutation altering the conserved size of the tRNAGln anticodon loop

C. Moraes, C. Tengan, R. Dey, 2000, Neuromuscular Disorders.

Oxidative phosphorylation dysfunction does not increase the rate of accumulation of age-related mtDNA deletions in skeletal muscle.

M. Zeviani, C. Moraes, S. Shanske, 1997, Mutation research.

Characterization of the estrous cycle in the Amazon spiny rat (Proechimys guyannensis)

E. Cavalheiro, C. Scorza, D. Amado, 2019, Heliyon.

[Periodic paralysis. Clinical analysis in 20 patients].

A. Gabbai, C. Tengan, A. S. de Oliveira, 1994, Arquivos de neuro-psiquiatria.

The role of nitric oxide in muscle fibers with oxidative phosphorylation defects.

A. Oliveira, A. Gabbai, B. Schmidt, 2007, Biochemical and biophysical research communications.

Evaluation of body composition in patients with migraine on prophylactic treatment with topiramate

T. R. Villa, C. Tengan, C. Caverni, 2021, Heliyon.

Effects of short-term zidovudine exposure on mitochondrial DNA content and succinate dehydrogenase activity of rat skeletal muscle cells

R. O. Godinho, C. Tengan, B. H. Kiyomoto, 2008, Journal of the Neurological Sciences.

NO control of mitochondrial function in normal and transformed cells.

C. Moraes, C. Tengan, 2017, Biochimica et biophysica acta. Bioenergetics.

A novel variant in the COX15 gene causing a fatal infantile cardioencephalomyopathy: a case report with clinical and molecular review.

F. Milanezi, C. Tengan, Eduardo Perrone, 2021, European journal of medical genetics.

Mitochondrial encephalomyopathy and hypoparathyroidism associated with a duplication and a deletion of mitochondrial deoxyribonucleic acid.

C. Moraes, M. Rocha, A. Gabbai, 1998, The Journal of clinical endocrinology and metabolism.

Andersen syndrome: an association of periodic paralysis, cardiac arrhythmia and dysmorphic abnormalities.

G. Prado, G. Manzano, A. Gabbai, 2006, Arquivos de neuro-psiquiatria.

Investigation of mitochondrial involvement in the experimental model of epilepsy induced by pilocarpine

E. Cavalheiro, I. Nasseh, M. Naffah-Mazzacoratti, 2006, Epilepsy Research.

Nitric Oxide in Skeletal Muscle: Role on Mitochondrial Biogenesis and Function

R. O. Godinho, C. Tengan, G. S. Rodrigues, 2012, International journal of molecular sciences.

The exercise test as a monitor of disease status in hypokalaemic periodic paralysis

G. Manzano, A. Gabbai, C. Tengan, 2004, Journal of Neurology, Neurosurgery & Psychiatry.

Isolated and painless infraspinatus atrophy in top-level volleyball players. Report of two cases and review of the literature.

A. Gabbai, C. Tengan, M. Morita, 1993, Arquivos de neuro-psiquiatria.

L-Arginine Reduces Nitro-Oxidative Stress in Cultured Cells with Mitochondrial Deficiency

C. Moraes, E. Higa, M. Mouro, 2021, Nutrients.

Progressive myopathy with a combined respiratory chain defect including Complex II

A. Oliveira, A. Gabbai, B. Schmidt, 2008, Journal of Neurological Sciences.

Neonatal mitochondrial encephaloneuromyopathy due to a defect of mitochondrial protein synthesis

S. Dimauro, D. Vivo, M. H. Barros, 2008, Journal of the Neurological Sciences.

Integrated analysis of the involvement of nitric oxide synthesis in mitochondrial proliferation, mitochondrial deficiency and apoptosis in skeletal muscle fibres

A. Oliveira, B. Schmidt, R. O. Godinho, 2016, Scientific Reports.

Duplication and triplication with staggered breakpoints in human mitochondrial DNA.

C. Moraes, C. Tengan, 1998, Biochimica et biophysica acta.

Mitochondrial DNA defects in Brazilian patients with chronic progressive external ophthalmoplegia

C. Moraes, A. Gabbai, C. Tengan, 1997, Journal of the Neurological Sciences.

Phenotype–genotype correlations in skeletal muscle of patients with mtDNA deletions

S. Dimauro, E. Schon, E. Ricci, 1995, Muscle & nerve. Supplement.

Frequency of dystrophic muscle abnormalities in chronic progressive external ophthalmoplegia: analysis of 86 patients

A. Gabbai, B. Schmidt, C. Tengan, 2006, Journal of Neurology, Neurosurgery & Psychiatry.

Mutations linked to familial hypokalaemic periodic paralysis in the calcium channel α1 subunit gene (Cav1·1) are not associated with thyrotoxic hypokalaemic periodic paralysis

J. Cerutti, G. Furuzawa, A. Gabbai, 2002, Clinical endocrinology.

Complex I spectrophotometric assay in cultured cells: detailed analysis of key factors.

C. Tengan, B. H. Kiyomoto, A. Rodrigues, 2013, Analytical biochemistry.

Nitric Oxide Synthesis Is Increased in Cybrid Cells with m.3243A>G Mutation

C. Moraes, C. Tengan, B. H. Kiyomoto, 2012, International journal of molecular sciences.

The mutations m.5628T>C and m.8348A>G in single muscle fibers of a patient with chronic progressive external ophthalmoplegia

A. Oliveira, A. Gabbai, B. Schmidt, 2012, Journal of the Neurological Sciences.

Detection and analysis of mitochondrial DNA deletions by whole genome PCR.

C. Moraes, C. Tengan, 1996, Biochemical and molecular medicine.

A. Oliveira, A. Gabbai, B. Schmidt, 2007, Journal of the Neurological Sciences.