Human Genome Epidemiology Literature Finder
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Records 1 - 14 (of 14 Records) |
| Query Trace: Crigler-Najjar Syndrome and UGT1A1[original query] |
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| Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects. Journal of gastroenterology and hepatology 2004 Sep 19 (9): 1023-8. Takeuchi Keisuke, Kobayashi Yoshinao, Tamaki Shigenori, Ishihara Tomoaki, Maruo Yoshihiro, Araki Jun, Mifuji Rumi, Itani Toshio, Kuroda Makoto, Sato Hiroshi, Kaito Masahiko, Adachi Yukihi |
| Frequencies of A(TA)7TAA, G71R, and G493R mutations of the UGT1A1 gene in the Malaysian population. Biology of the neonate 2006 89 (3): 171-6. Yusoff Surini, Van Rostenberghe Hans, Yusoff Narazah M, Talib Norlelawati A, Ramli Noraida, Ismail N Zainal A N, Ismail W Pauzi W, Matsuo Masafumi, Nishio Hisahi |
| Regression Modeling and Meta-Analysis of Diagnostic Accuracy of SNP-Based Pathogenicity Detection Tools for UGT1A1 Gene Mutation. Genetics research international 2013 2013 . Rahim F, Galehdari H, Mohammadi-Asl J, Saki N |
| [Mutation analysis of UGT1A1 gene in patients with unconjugated hyperbilirubinemia]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2013 Aug 30 (4): 425-8. Sun Shun-chang, Zhou Zhi-ming, Chen Qun-rong, Peng Yun-sheng, Tu Chuan-qi |
| 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 |
| UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children: A retrospective analysis and quantitative correlation. Medicine 2018 Dec 97 (49): e13576. Abuduxikuer Kuerbanjiang, Fang Ling-Juan, Li Li-Ting, Gong Jing-Yu, Wang Jian-S |
| [Study on spectrum of UGT1A1 mutations in connection with inherited non-hemolytic unconjugated hyperbilirubinemia]. Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology 2019 1 26 (12): 898-902. Xiong Q F, Zhong Y D, Feng X N, Zhou H, Liu D X, Wu X P, Yang Y |
| 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- |
| Bilirubin metabolism and UDP-glucuronosyltransferase 1A1 variants in Asians: Pathogenic implications and therapeutic response. The Kaohsiung journal of medical sciences 2022 8 38 (8): 729-738. Huang May-Jen, Chen Pei-Lain, Huang Ching-Sh |
| Gilbert Syndrome and Genetic Findings in Children: A Tertiary-Center Experience from Turkey. Turkish archives of pediatrics 2022 7 57 (3): 295-299. Ça?an Appak Yeliz, Aksoy Betül, Özy?lmaz Berk, Özdemir Taha Re?id, Baran Ma?all |
| Novel combined UGT1A1 mutations in Crigler Najjar Syndrome type I. Journal of clinical laboratory analysis 2022 Jun 36 (6): e24482. Abdellaoui Nawel, Abdelmoula Balkiss, Abdelhedi Rania, Kharrat Najla, Tabebi Mouna, Rebai Ahmed, Bouayed Abdelmoula Nou |
| Gilbert or Crigler-Najjar syndrome? Neonatal severe unconjugated hyperbilirubinemia with P364L UGT1A1 homozygosity. Italian journal of pediatrics 2022 4 48 (1): 59. Cozzi Laura, Nuti Federica, Degrassi Irene, Civeriati Daniela, Paolella Giulia, Nebbia Gabriel |
| [A family study of the compound heterozygous mutation of the UGT1A1 gene causing Crigler-Najjar syndrome type II]. Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology 2023 5 31 (2): 168-173. L Luo, X B Yao, S J Zheng, W L Ya |
| Analysis of UGT1A1 genotype-phenotype correlation in Chinese patients with gilbert and crigler-Najjar II syndrome. European journal of medical genetics 2024 7 71 104962. Lina Wu, Zhenkun Li, Yi Song, Yanmeng Li, Wei Zhang, Xuemei Zhong, Xiaoming Wang, Jian Huang, Xiaojuan |
- Page last reviewed:Feb 1, 2024
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