Shigeru Fukuyama

Novel Mutations of the Chloride Channel Kb Gene in Two Japanese Patients Clinically Diagnosed as Bartter Syndrome with Hypocalciuria

Shigeru Fukuyama, Misako Hiramatsu, Motohiro Akagi et al. · The Journal of Clinical Endocrinology & Metabolism · 2004 · 61 citations

Life Sciences, Genetics, Molecular Genetics +17

Analysis of renal tubular electrolyte transporter genes in seven patients with hypokalemic metabolic alkalosis

Shigeru Fukuyama, Shoko Okudaira, Syosin Yamazato et al. · Kidney International · 2003 · 47 citations · Full text

Medicine, Nephrology, Physiology +13

Effect of Trp64Arg mutation of the β3‐adrenergic receptor gene and C161T substitution of the peroxisome proliferator activated receptor γ gene on obesity in Japanese children

Rina Arashiro, Keisuke Katsuren, Shigeru Fukuyama et al. · Pediatrics International · 2003 · 26 citations

Medicine, Genetics, Molecular Genetics +15

Effect of a Common Mutation (D442G) of the Cholesteryl Ester Transfer Protein Gene on Lipids and Lipoproteins in Children

Rina Arashiro, Keisuke Katsuren, Kyu Kyu Maung et al. · Pediatric Research · 2001 · 18 citations

Life Sciences, Genetics, Molecular Genetics +14

The influence of the acyl-CoA:cholesterol acyltransferase-1 gene (−77G→A) polymorphisms on plasma lipid and apolipoprotein levels in normolipidemic and hyperlipidemic subjects

Takao Ohta, Kouki Takata, Keisuke Katsuren et al. · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · 2004 · 12 citations

Life Sciences, Genetics, Molecular Genetics +12