Kazuhiro Akaba

Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate‐glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese

Kazuhiro Akaba, Toshiyuki Kimura, Ayako Sasaki et al. · IUBMB Life · 1998 · 209 citations

Molecular analysis of congenital central hypoventilation syndrome

Ayako Sasaki, Masayo Kanai, Kazuki Kijima et al. · Human Genetics · 2003 · 181 citations

Genetic Disorder, Molecular Analysis, Physiology +2

Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese

Kazuhiro Akaba, Toshiyuki Kimura, Ayako Sasaki et al. · Journal of Human Genetics · 1999 · 97 citations · Full text

Neonatal Hyperbilirubinemia in Japanese Neonates: Analysis of the Heme Oxygenase-1 Gene and Fetal Hemoglobin Composition in Cord Blood

Masayo Kanai, Kazuhiro Akaba, Ayako Sasaki et al. · Pediatric Research · 2003 · 35 citations · Full text

Heme Oxygenase-1 Gene, Japanese Neonates, Heme Degradation +7

Congenital Central Hypoventilation Syndrome: A Novel Mutation of the RET Gene in an Isolated Case.

Masayo Kanai, Chikahiko Numakura, Ayako Sasaki et al. · The Tohoku Journal of Experimental Medicine · 2002 · 25 citations · Full text

Developmental Anomaly, Novel Mutation, Isolated Case +15