Item talk:Q167505

{

 "OpenAlex": {
   "display_name": "Management of Hyperbilirubinemia in Newborn Infants",
   "description": "This cluster of papers focuses on the management, genetic aspects, and complications of hyperbilirubinemia in newborn infants. It covers topics such as glucose-6-phosphate dehydrogenase deficiency, neonatal jaundice, bilirubin metabolism, kernicterus, phototherapy, UGT1A1 gene mutations, neurotoxicity, bilirubin measurement methods, genetic variants associated with hyperbilirubinemia, and the importance of newborn screening programs.",
   "keywords": [
     "Glucose-6-Phosphate Dehydrogenase Deficiency",
     "Neonatal Jaundice",
     "Bilirubin Metabolism",
     "Kernicterus",
     "Phototherapy",
     "UGT1A1 Gene",
     "Neurotoxicity",
     "Bilirubin Measurement",
     "Genetic Variants",
     "Newborn Screening"
   ],
   "ids": {
     "openalex": "https://openalex.org/T12068",
     "wikipedia": "https://en.wikipedia.org/wiki/Neonatal_hyperbilirubinemia"
   },
   "subfield": {
     "id": "https://openalex.org/subfields/2735",
     "display_name": "Pediatrics, Perinatology and Child Health"
   },
   "field": {
     "id": "https://openalex.org/fields/27",
     "display_name": "Medicine"
   },
   "domain": {
     "id": "https://openalex.org/domains/4",
     "display_name": "Health Sciences"
   },
   "updated_date": "2024-08-12T06:04:48.714323",
   "created_date": "2024-01-23",
   "type": "topic",
   "oa_id": "T12068",
   "id": "https://openalex.org/T12068"
 }

}