Kenichi Satomura

Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome

Mayumi Sako, Koichi Nakanishi, Mina Obana et al. · Kidney International · 2005 · 91 citations

Glomerulonephritis, Urology, Genetic Disorder +9

PAX2 Gene Mutation in a Family with Isolated Renal Hypoplasia

Kaori Nishimoto, Kazumoto Iijima, Taku Shirakawa et al. · Journal of the American Society of Nephrology · 2001 · 75 citations

Identification of novel missense mutations (Phe310Leu and Gly439Arg) in a neonatal case of hypophosphatasia.

Keiichi Ozono, Masayo Yamagata, Toshimi Michigami et al. · The Journal of Clinical Endocrinology & Metabolism · 1996 · 71 citations

Biology, Serum Alkaline Phosphatase, Mendelian Disorder +15

NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children

Kyoko Maruyama, Kazumoto Iijima, Masahiro Ikeda et al. · Pediatric Nephrology · 2003 · 70 citations

Genetic Disorder, Medicine, Genetics +7

The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune?Albright syndrome

Takehisa Yamamoto, Yasuo Imanishi, Eiichi Kinoshita et al. · Journal of Bone and Mineral Metabolism · 2005 · 66 citations

Metabolic Syndrome, Metabolic Disorder, Vitamin D Metabolism +10