Kayoko Sudo

Lactate dehydrogenase M-subunit deficiency: a new type of hereditary exertional myopathy

Takashi Kanno, Kayoko Sudo, Masato Maekawa et al. · Clinica Chimica Acta · 1988 · 146 citations

Mitochondrial Myopathy, Mendelian Disorder, New Type +6

Hereditary deficiency of lactate dehydrogenase M-subunit

Kanno Takashi, Kayoko Sudo, Izumi Takeuchi et al. · Clinica Chimica Acta · 1980 · 137 citations

Biochemistry, Genetic Disorder, Hereditary Deficiency +3

Molecular characterization of genetic mutation in human lactate dehydrogenase-A (M) deficiency

Masato Maekawa, Kayoko Sudo, Takashi Kanno et al. · Biochemical and Biophysical Research Communications · 1990 · 58 citations

Genetic Analysis, Molecular Characterization, Mendelian Disorder +10

Genetic mutations of butyrylcholine esterase identified from phenotypic abnormalities in Japan

Masato Maekawa, Kayoko Sudo, Dilip Dey et al. · Clinical Chemistry · 1997 · 47 citations · Full text

Estimation of the gene frequency of lactate dehydrogenase subunit deficiencies.

Masato Maekawa, Shinji Kanda, Kayoko Sudo et al. · PubMed · 1984 · 41 citations