Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: Hemolysis and UGT1A1[original query] |
---|
(TA)n UGT 1A1 promoter polymorphism: a crucial factor in the pathophysiology of jaundice in G-6-PD deficient neonates. Pediatric research 2007 Jun 61 (6): 727-31. Kaplan Michael, Renbaum Paul, Vreman Hendrik J, Wong Ronald J, Levy-Lahad Ephrat, Hammerman Cathy, Stevenson David |
The effect of UGT1A1 promoter polymorphism on bilirubin response to hydroxyurea therapy in hemoglobinopathies. Clinical biochemistry 2010 Nov 43 (16-17): 1329-32. Italia Khushnooma Y, Jijina Farah F, Jain Dipty, Merchant Rashid, Nadkarni Anita H, Mukherjee Malay, Ghosh Kanjaksha, Colah Roshan |
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
PloS one 2012 7 (4): e34741. Milton Jacqueline N, Sebastiani Paola, Solovieff Nadia, Hartley Stephen W, Bhatnagar Pallav, Arking Dan E, Dworkis Daniel A, Casella James F, Barron-Casella Emily, Bean Christopher J, Hooper W Craig, DeBaun Michael R, Garrett Melanie E, Soldano Karen, Telen Marilyn J, Ashley-Koch Allison, Gladwin Mark T, Baldwin Clinton T, Steinberg Martin H, Klings Elizabeth |
UGT1A1 promoter polymorphism associated with serum bilirubin level in Saudi patients with sickle cell disease. Annals of Saudi medicine 0 33 (4): 372-6. Hamad Zainab, Aljedai Abdullah, Halwani Rabih, AlSultan Abdulrahm |
Severe neonatal hyperbilirubinemia and UGT1A1 promoter polymorphism. The Journal of pediatrics 2014 Jul 165 (1): 42-5. Travan Laura, Lega Sara, Crovella Sergio, Montico Marcella, Panontin Elisa, Demarini Serg |
Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1. Hematology (Amsterdam, Netherlands) 2015 Jul . Chaouch Leila, Kalai1 Miniar, Darragi Imen, Boudrigua Imen, Chaouachi Dorra, Ammar Slim Ben, Mellouli F, Bjaoui M, Abbes Sal |
Spectrum of UGT1A1 Variations in Chinese Patients with Crigler-Najjar Syndrome Type II. PloS one 2015 10 (5): e0126263. Li Lufeng, Deng Guohong, Tang Yi, Mao Qi |
Frequency of the UGT1A1*28 Polymorphism in a Romanian Cohort of Gilbert Syndrome Individuals. Journal of gastrointestinal and liver diseases : JGLD 2017 Mar 26 (1): 25-28. Radoi Viorica E, Ursu Radu I, Poenaru Elena, Arsene Cosmin, Bohiltea Camil L, Bohiltea Roxa |
Study of Gilbert's Syndrome-Associated UGT1A1 Polymorphism in Jaundiced Neonates of ABO Incompatibility Hemolysis Disease. American journal of perinatology 2019 May . Yu Yingfang, Du Lizhong, Chen An, Chen Lih |
A high frequency of Gilbert syndrome (UGT1A1*28/*28) and associated hyperbilirubinemia but not cholelithiasis in adolescent and adult north Indian patients with transfusion-dependent ?-thalassemia. Annals of hematology 2020 7 99 (9): 2019-2026. Shrestha Oshan, Khadwal Alka Rani, Singhal Manphool, Trehan Amita, Bansal Deepak, Jain Richa, Pal Arnab, Hira Jasbir Kaur, Chhabra Sanjeev, Malhotra Pankaj, Das Reena, Sharma Prasha |
Genetic Factors and Delayed TSB Monitoring and Treatment as Risk Factors Associated with Severe Hyperbilirubinemia in Term Neonates Admitted for Phototherapy. Journal of tropical pediatrics 2020 6 66 (6): 569-582. Boo Nem-Yun, Sin Shwe, Chee Seok-Chiong, Mohamed Maslina, Ahluwalia Anita Kaur, Ling Michelle Min-Min, Ong Han-Ki |
Carbon monoxide breath test assessment of mild hemolysis in Gilbert's syndrome. Medicine 2020 2 99 (7): e19109. Kang Ling-Ling, Ma Yong-Jian, Zhang Hou- |
UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China. BMC pediatrics 2021 06 21 (1): 259. Yang Hui, Lin Fen, Chen Zi-Kai, Zhang Lin, Xu Jia-Xin, Wu Yong-Hao, Gu Jing-Ying, Ma Yu-Bin, Li Jian-Dong, Yang Li- |
[Gilbert's syndrome: hyperbilirubinemia enemy or friend]. Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology 2021 11 29 (10): 1024-1027. Xiang G Q, Sun F R, Wang B |
Clinical and genetic risk factors associated with neonatal severe hyperbilirubinemia: a case-control study based on the China Neonatal Genomes Project. Frontiers in genetics 2024 1 14 1292921. Xiao Wang, Tiantian Xiao, Jin Wang, Bingbing Wu, Huijun Wang, Yulan Lu, Yaqiong Wang, Bin Chen, Liyuan Hu, Yun Cao, Rong Zhang, Guoqiang Cheng, Laishuan Wang, Zhihua Li, Xinran Dong, Lin Yang, Wenhao Zh |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: