HuGE Literature Finder
Records 1-6
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Case-controlled study on indirect hyperbilirubinemia in exclusively breast fed neonates and mutations of the bilirubin Uridine Diphosphate-Glucuronyl transferase gene 1A1.
Annals of medicine and surgery (2012) 2017 Jan 13 6-12. Mohammed Amal E, Behiry Eman G, El-Sadek Akram E, Abdulghany Waleed E, Mahmoud Dalia M, Elkholy Abdelfattah |
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Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms.
Journal of human genetics 2015 Jan 60 (1): 35-40. Sato Hiroko, Uchida Toshihiko, Toyota Kentaro, Nakamura Tomohiro, Tamiya Gen, Kanno Miyako, Hashimoto Taeko, Watanabe Masashi, Aoki Kuraaki, Hayasaka Kiyos |
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UGT1A1 gene variants and clinical risk factors modulate hyperbilirubinemia risk in newborns.
Journal of perinatology : official journal of the California Perinatal Association 2014 Feb 34 (2): 120-4. Tiwari P K, Bhutada A, Agarwal R, Basu S, Raman R, Kumar |
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Heme oxygenase-1 gene variants and hyperbilirubinemia risk in North Indian newborns.
European journal of pediatrics 2013 Dec 172 (12): 1627-32. Tiwari Pankaj Kumar, Sethi Amanpreet, Basu Sriparna, Raman Rajiva, Kumar Ash |
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Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feeding.
Journal of human genetics 2013 Jan 58 (1): 7-10. Sato Hiroko, Uchida Toshihiko, Toyota Kentaro, Kanno Miyako, Hashimoto Taeko, Watanabe Masashi, Nakamura Tomohiro, Tamiya Gen, Aoki Kuraaki, Hayasaka Kiyos |
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211 G to a variation of UDP-glucuronosyl transferase 1A1 gene and neonatal breastfeeding jaundice.
Pediatric research 2011 Feb 69 (2): 170-4. Chou Hung-Chieh, Chen Mei-Huei, Yang Hwai-I, Su Yi-Ning, Hsieh Wu-Shiun, Chen Chien-Yi, Chen Huey-Ling, Chang Mei-Hwei, Tsao Po-Ni |
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