The exercise test as a monitor of disease status in hypokalaemic periodic paralysis von Tengan, C H, Antunes, A C, Gabbai, A A, Manzano, G M

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Frequency of dystrophic muscle abnormalities in chronic progressive external ophthalmoplegia: analysis of 86 patients von Kiyomoto, B H, Tengan, C H, Costa, C K, Oliveira, A S, Schmidt, B, Gabbai, A A

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Mitochondrial DNA defects in Brazilian patients with chronic progressive external ophthalmoplegia von Kiyomoto, B.H, Tengan, C.H, Moraes, C.T, Oliveira, A.S.B, Gabbai, A.A

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Phenotype-genotype correlations in skeletal muscle of patients with mtDNA deletions von Moraes, C. T., Sciacco, M., Ricci, E., Tengan, C. H., Hao, H., Bonilla, E., Schon, E. A., DiMauro, S.

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Mitochondrial encephalomyopathy and hypoparathyrodism associated with a duplication and a deletion of mitochondrial deoxyribonucleic acid von TENGAN, C. H, KIYOMOTO, B. H, ROCHA, M. S, TAVARES, V. L. S, GABBAI, A. A, MORAES, C. T

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Duplication and triplication with staggered breakpoints in human mitochondrial DNA von Tengan, Célia H, Moraes, Carlos T

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Mitochondrial encephalomyopathy and hypoparathyroidism associated with a duplication and a deletion of mitochondrial deoxyribonucleic acid von Tengan, C H, Kiyomoto, B H, Rocha, M S, Tavares, V L, Gabbai, A A, Moraes, C T

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A novel myopathy-associated mitochondrial DNA mutation altering the conserved size of the tRNA(Gln) anticodon loop von Dey, R, Tengan, C H, Morita, M P, Kiyomoto, B H, Moraes, C T

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Isolated and painless infraspinatus atrophy in top-level volleyball players. Report of two cases and review of the literature von Tengan, C H, Oliveira, A S, Kiymoto, B H, Morita, M P, De Medeiros, J L, Gabbai, A A

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Andersen syndrome: an association of periodic paralysis, cardiac arrhythmia and dysmorphic abnormalities von Tengan, Célia H, Antunes, Antonio C, Bauab, José R, Baubab, José R, Prado, Gilmar F, Manzano, Gilberto M, Gabbai, Alberto A

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Investigation of mitochondrial involvement in the experimental model of epilepsy induced by pilocarpine von Nasseh, Ibrahim Elias, Amado, Débora, Cavalheiro, Esper A., da Graça Naffah-Mazzacoratti, Maria, Tengan, Célia Harumi

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Detection and Analysis of Mitochondrial DNA Deletions by Whole Genome PCR von Tengan, Célia H., Moraes, Carlos T.

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Frequency of duplications in the D-loop in patients with mitochondrial DNA deletions von Tengan, Célia H, Ferreiro-Barros, Claudia, Cardeal, Marina, Fireman, Moacir A.T, Oliveira, Acary S.B, Kiyomoto, Beatriz H, Gabbai, Alberto A

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Mitochondrial Encephalomyopathy and Hypoparathyrodism Associated with a Duplication and a Deletion of Mitochondrial Deoxyribonucleic Acid1 von Tengan, C. H, Kiyomoto, B. H, Rocha, M. S, Tavares, V. L. S, Gabbai, A. A, Moraes, C. T

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Mitochondrial Encephalomyopathy and Hypoparathyrodism Associated with a Duplication and a Deletion of Mitochondrial Deoxyribonucleic Acid 1 von Tengan, C. H., Kiyomoto, B. H., Rocha, M. S., Tavares, V. L. S., Gabbai, A. A., Moraes, C. T.

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Periodic paralysis. Clinical analysis in 20 patients von Tengan, C H, De Oliveira, A S, Gabbai, A A

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Periodic paralysis: anatomo-pathological study of skeletal muscles in 14 patients von Tengan, C H, Oliveira, A S, Morita, M da P, Kiyomoto, B H, Schmidt, B, Gabbai, A A

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Periodic paralysis. Clinical analysis in 20 patients von Tengan, C H, De Oliveira, A S, Gabbai, A A

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Paralisia periódica: estudo anátomo-patológico do músculo esquelético de 14 pacientes von Tengan, Célia Harumi, Oliveira, Acary Souza Bulle, Morita, Maria da Penha Ananias, Kiyomoto, Beatriz Hitomi, Schmidt, Beny, Gabbai, Alberto Alain

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Distal renal tubular acidosis presenting with rhabdomyolysis von Zanoteli, E, De Oliveira, A S, Tengan, C H, Morita, M P, Schmidt, B, Gabbai, A A

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