Found: 10
Select item for more details and to access through your institution.
Molecular analysis of congenital central hypoventilation syndrome.
- Published in:
- Human Genetics, 2003, v. 114, n. 1, p. 22, doi. 10.1007/s00439-003-1036-z
- By:
- Publication type:
- Article
Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese.
- Published in:
- Journal of Human Genetics, 1999, v. 44, n. 1, p. 22, doi. 10.1007/s100380050100
- By:
- Publication type:
- Article
Correlation between magnesium sulphate exposure in utero and serum calcium and alkaline phosphatase levels in preterm infants.
- Published in:
- Magnesium Research, 2022, v. 35, n. 4, p. 118, doi. 10.1684/mrh.2023.0509
- By:
- Publication type:
- Article
Characteristics of nonoliguric hyperkalemia in preterm infants: A case‐control study in a single center.
- Published in:
- Pediatrics International, 2020, v. 62, n. 5, p. 576, doi. 10.1111/ped.14115
- By:
- Publication type:
- Article
Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese.
- Published in:
- IUBMB Life, 1998, v. 46, n. 1, p. 21, doi. 10.1080/15216549800203512
- By:
- Publication type:
- Article
Heparin-Induced Hyperkalemia in an Extremely-Low-Birth-Weight Infant: A Case Report.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2014, v. 6, n. 2, p. 125, doi. 10.4274/jcrpe.1255
- By:
- Publication type:
- Article
Late-Onset Glucocorticoid-Responsive Circulatory Collapse in Preterm Infants: Clinical Characteristics of 14 Patients.
- Published in:
- Tohoku Journal of Experimental Medicine, 2015, v. 235, n. 3, p. 241, doi. 10.1620/tjem.235.241
- By:
- Publication type:
- Article
Premature rupture of membranes and neonatal respiratory morbidity at 32-41 weeks' gestation: A retrospective single-center cohort study.
- Published in:
- Journal of Obstetrics & Gynaecology Research, 2015, v. 41, n. 8, p. 1193, doi. 10.1111/jog.12689
- By:
- Publication type:
- Article
Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene: The common−3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese.
- Published in:
- Pediatrics International, 2005, v. 47, n. 2, p. 137, doi. 10.1111/j.1442-200x.2005.02030.x
- By:
- Publication type:
- Article
Mutation analysis of phenylketonuria in Yamagata prefecture, Japan.
- Published in:
- Pediatrics International, 2001, v. 43, n. 1, p. 1, doi. 10.1046/j.1442-200X.2001.01336.x
- By:
- Publication type:
- Article