Fusako Komoda

The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia

Fusako Komoda, Takashi Sekine, Jun Inatomi et al. · Pediatric Nephrology · 2004 · 82 citations

Urology, Renal Function, W258x Mutation +10

Mutational analysis of idiopathic renal hypouricemia in Korea

Hae Il Cheong, Ju Hyung Kang, Joo Hoon Lee et al. · Pediatric Nephrology · 2005 · 78 citations

Glomerular Disease, Urology, Renal Disease +7

Japanese Dent disease has a wider clinical spectrum than Dent disease in Europe/USA: genetic and clinical studies of 86 unrelated patients with low-molecular-weight proteinuria

Takashi Sekine, Fusako Komoda, Kenichiro Miura et al. · Nephrology Dialysis Transplantation · 2013 · 68 citations

Unrelated Patients, Genetics, Genetic Epidemiology +18

Development and clinical application of high performance liquid chromatography for the simultaneous determination of plasma levels of theophylline and its metabolites without interference from caffeine

Junko Kizu, Shigekazu Watanabe, Nobuhiro Yasuno et al. · Biomedical Chromatography · 1999 · 27 citations