HuGE Literature Finder
Records 1-24
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Economic evaluation of point of care universal newborn screening for glucose-6-Phosphate dehydrogenase deficiency in United States.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2021 2 1-9. Vidavalur Ramesh, Bhutani Vinod |
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G6PD genetic variations in neonatal Hyperbilirubinemia in Indonesian Deutromalay population.
BMC pediatrics 2019 Dec 19 (1): 506. Wisnumurti Dewi A, Sribudiani Yunia, Porsch Robert M, Maskoen Ani M, Rahayuningsih Sri E, Asni Eni K, Sleutels Frank, van Ijcken Wilfred F J, Sukadi Abdurachman, Achmad Tri |
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Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study.
BioMed research international 2018 2018 7803175. Zhou Jinfu, Yang Changyi, Zhu Wenbin, Chen Shuwei, Zeng Yinglin, Wang Jing, Zhao Hong, Chen Yao, Lin Fe |
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Risk assessment of gene variants for neonatal hyperbilirubinemia in Taiwan.
BMC pediatrics 2016 16 (1): 144. Weng Yi-Hao, Chiu Ya-Wen, Cheng Shao-Wen, Yang Chun-Y |
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Clinical Significance of UGT1A1 Genetic Analysis in Chinese Neonates with Severe Hyperbilirubinemia.
Pediatrics and neonatology 2015 Dec . Yang Hui, Wang Qian, Zheng Lei, Zheng Xiang-Bin, Lin Min, Zhan Xiao-Fen, Yang Li- |
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Relation between Neonatal Icter and Gilbert Syndrome in Gloucose-6-Phosphate Dehydrogenase Deficient Subjects.
Journal of clinical and diagnostic research : JCDR 2014 Mar 8 (3): 63-5. Zahedpasha Yadollah, Ahmadpour Mousa, Niaki Haleh Akhavan, Alaee Ehs |
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Identifying term breast-fed infants at risk of significant hyperbilirubinemia.
Pediatric research 2013 Oct 74 (4): 408-12. Chang Pi-Feng, Lin Yu-Cheng, Liu Kevin, Yeh Shu-Jen, Ni Yen-Hsu |
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Risk factors associated with unconjugated neonatal hyperbilirubinemia in Malaysian neonates.
Journal of tropical pediatrics 2013 Aug 59 (4): 280-5. Wong Feiliang, Boo NemYun, Othman Aino |
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[Genetic factors in the occurrence of neonatal unconjugated hyperbilirubinemia].
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2012 Apr 14 (4): 256-9. Sun Ling-Ling, Chen Yun-Sheng, Yu Zhen-Zhu, Huang Bao-Xing, Xu Gang, Ma Dong-Li, Li Chang-Gang, Liu Lei, Liu Xiao-Ho |
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Prevalence of uridine glucuronosyl transferase 1A1 (UGT1A1) mutations in Malay neonates with severe jaundice.
The Malaysian journal of pathology 2011 Dec 33 (2): 95-100. Azlin I, Wong F L, Ezham M, Hafiza A, Ainoon |
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Risk of hyperbilirubinemia in breast-fed infants.
The Journal of pediatrics 2011 Oct 159 (4): 561-5. Chang Pi-Feng, Lin Yu-Cheng, Liu Kevin, Yeh Shu-Jen, Ni Yen-Hsu |
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Clinical and genetic risk factors for moderate hyperbilirubinemia in Brazilian newborn infants.
Journal of perinatology : official journal of the California Perinatal Association 2010 Dec 30 (12): 819-26. Mezzacappa M A, Facchini F P, Pinto A C, Cassone A E L, Souza D S, Bezerra M A C, Albuquerque D M, Saad S T O, Costa F |
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Variants of organic anion transporter polypeptide 2 gene are not risk factors associated with severe neonatal hyperbilirubinemia.
The Malaysian journal of pathology 2009 Dec 31 (2): 99-104. Wong Fei-Liang, Boo Nem-Yun, Ainoon Othman, Wang May-K |
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Complex multifactorial nature of significant hyperbilirubinemia in neonates.
Pediatrics 2009 Nov 124 (5): e868-77. Watchko Jon F, Lin Zhili, Clark Reese H, Kelleher Amy S, Walker M Whit, Spitzer Alan R, |
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Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia.
Pediatrics international : official journal of the Japan Pediatric Society 2009 Aug 51 (4): 488-93. Boo Nem-Yun, Wong Fei-Liang, Wang May-Kay, Othman Aino |
Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia.
Human molecular genetics 2009 Jul 18 (14): 2711-8. Sanna Serena, Busonero Fabio, Maschio Andrea, McArdle Patrick F, Usala Gianluca, Dei Mariano, Lai Sandra, Mulas Antonella, Piras Maria Grazia, Perseu Lucia, Masala Marco, Marongiu Mara, Crisponi Laura, Naitza Silvia, Galanello Renzo, Abecasis Gonçalo R, Shuldiner Alan R, Schlessinger David, Cao Antonio, Uda Manue |
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UGT1A1 gene polymorphisms in North Indian neonates presenting with unconjugated hyperbilirubinemia.
Pediatric research 2009 Jun 65 (6): 675-80. Agrawal Sunil K, Kumar Praveen, Rathi Ritu, Sharma Neeraj, DAS Reena, Prasad Rajendra, Narang An |
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Coexpression of gene polymorphisms involved in bilirubin production and metabolism.
Pediatrics 2008 Jul 122 (1): e156-62. Lin Zhili, Fontaine Jamie, Watchko Jon |
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Genetic factors related to unconjugated hyperbilirubinemia amongst adults.
Pharmacogenetics and genomics 2005 Jan 15 (1): 43-50. Huang Ching-Shan, Huang May-Jen, Lin Min-Shung, Yang Sien-Sing, Teng Hsiu-Chen, Tang Kung-She |
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Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Malays.
Human mutation 2003 Jan 21 (1): 101. Ainoon O, Yu Y H, Amir Muhriz A L, Boo N Y, Cheong S K, Hamidah N |
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Coinheritance of variant UDP-glucuronosyl transferase 1A1 gene and glucose-6-phosphate dehydrogenase deficiency in adults with hyperbilirubinemia.
Pharmacogenetics 2002 Nov 12 (8): 663-6. Huang May-Jen, Yang Yi-Chu, Yang Sien-Sing, Lin Min-Shung, Chen En-Sung, Huang Ching-Sh |
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Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia.
Gastroenterology 2002 Jul 123 (1): 127-33. Huang Ching-Shan, Chang Pi-Feng, Huang May-Jen, Chen En-Sung, Chen Wu-Char |
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Glucose-6-phosphate dehydrogenase (G6PD) mutations in Thailand: G6PD Viangchan (871G>A) is the most common deficiency variant in the Thai population.
Human mutation 2002 Feb 19 (2): 185. Nuchprayoon I, Sanpavat S, Nuchprayoon |
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[Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert syndrome].
Acta médica portuguesa 0 15 (6): 409-12. Costa Elísio, Vieira Emilia, Cleto Esmeralda, Cabeda José M, Pinho Luciana, Coimbra Eduarda, Dos Santos Rosário, Barbot Jo |
- Page last reviewed:Oct 1, 2020
- Page last updated:Mar 05, 2021
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