Célia Harumi Tengan

Mutations linked to familial hypokalaemic periodic paralysis in the calcium channel α1 subunit gene (Ca_v1·1) are not associated with thyrotoxic hypokalaemic periodic paralysis

Magnus R. Dias‐da‐Silva, Janete M. Cerutti, Célia Harumi Tengan et al. · Clinical Endocrinology · 2002 · 50 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

Célia Harumi Tengan · Journal of Neurology Neurosurgery & Psychiatry · 2004 · 41 citations · Full text

Medicine, Endocrinology, Physiology +16

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

Célia Harumi Tengan, Beatriz Hitomi Kiyomoto, Rosely Oliveira Godinho et al. · Biochemical and Biophysical Research Communications · 2007 · 35 citations

Life Sciences, Biochemistry, Physiology +15

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

Carlos T. Moraes, Monica Sciacco, Enzo Ricci et al. · Muscle & Nerve · 1995 · 35 citations

Life Sciences, Genetics, Molecular Genetics +17

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

Célia Harumi Tengan, Alberto Alain Gabbai, Sara Shanske et al. · Mutation research. Fundamental and molecular mechanisms of mutagenesis · 1997 · 31 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17