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Select item 110157041.

Prolonged Jaundice in a Premature Breastfed Infant With Gilbert’s Syndrome

Frances Strobl, Melissa Ann Theurich

J Hum Lact. 2024 May; 40(2): 270–275. Published online 2024 Feb 9. doi: 10.1177/08903344241227226

PMCID:: PMC11015704

Article PDF–1.0M

Select item 105194832.

Clinical and genetic definition of serum bilirubin levels for the diagnosis of Gilbert syndrome and hypobilirubinemia

Thierry Poynard, Olivier Deckmyn, Valentina Peta, Mehdi Sakka, Pascal Lebray, Joseph Moussalli, Raluca Pais, Chantal Housset, Vlad Ratziu, Eric Pasmant, Dominique Thabut

Hepatol Commun. 2023 Oct; 7(10): e0245. Published online 2023 Sep 22. doi: 10.1097/HC9.0000000000000245

PMCID:: PMC10519483

Article PDF–1.6M

Select item 103421363.

Association of Low Serum Bilirubin Concentrations and Promoter Variations in the UGT1A1 and HMOX1 Genes with Type 2 Diabetes Mellitus in the Czech Population

Alena Jirásková, Jan Škrha, Libor Vítek

Int J Mol Sci. 2023 Jul; 24(13): 10614. Published online 2023 Jun 25. doi: 10.3390/ijms241310614

PMCID:: PMC10342136

Article PDF–272K

Select item 98767094.

A Novel SPTA1 Mutation in a Patient with Hereditary Spherocytosis without a Family History and Coexisting Gilbert's Syndrome

Yuma Nato, Yuki Kageyama, Kazutaka Suzuki, Keiko Shimojima Yamamoto, Hitoshi Kanno, Hiroyuki Miyashita

Intern Med. 2023 Jan 1; 62(1): 107–111. Published online 2022 May 31. doi: 10.2169/internalmedicine.9478-22

PMCID:: PMC9876709

Article PDF–545K

Select item 98380135.

Stefanie V. Junk, Elke Schaeffeler, Martin Zimmermann, Anja Möricke, Rita Beier, Peter Schütte, Birthe Fedders, Julia Alten, Laura Hinze, Norman Klein, Andreas Kulozik, Martina U. Muckenthaler, Rolf Koehler, Arndt Borkhardt, Jayaram Vijayakrishnan, David Ellinghaus, Michael Forster, Andre Franke, Astrid Wintering, Christian P. Kratz, Martin Schrappe, Matthias Schwab, Richard S. Houlston, Gunnar Cario, Martin Stanulla

J Exp Clin Cancer Res. 2023; 42: 21. Published online 2023 Jan 13. doi: 10.1186/s13046-022-02585-x

PMCID:: PMC9838013

Article PDF–2.4M

Select item 98127676.

Concurrence of novel mutations causing Gilbert’s and Dubin–Johnson syndrome with poor clinical outcomes in a Han Chinese family

Tai-Cheng Zhou, Xiao Li, Hui Li, Feng-Wei Liu, Si-Hang Zhang, Jing-Hua Fan, Wen-Xiu Yang, Ya-Li Yang, Liang Zhang, Jia Wei

J Hum Genet. 2023; 68(1): 17–23. Published online 2022 Oct 24. doi: 10.1038/s10038-022-01086-1

PMCID:: PMC9812767

Article PDF–1.8M

Select item 96038747.

The Mutation Hotspots at UGT1A Locus May Be Associated with Gilbert’s Syndrome Affecting the Taiwanese Population

Paul Wei-Che Hsu, Po-Cheng Liao, Yu-Hsiang Kao, Xin-Yu Lin, Rong-Nan Chien, Chau-Ting Yeh, Chi-Chun Lai, Yu-Chiau Shyu, Chih-Lang Lin

Int J Mol Sci. 2022 Oct; 23(20): 12709. Published online 2022 Oct 21. doi: 10.3390/ijms232012709

PMCID:: PMC9603874

Article PDF–1.3M

Select item 93107288.

Sexual dimorphism: increased sterol excretion leads to hypocholesterolaemia in female hyperbilirubinaemic Gunn rats

Josif Vidimce, Johara Pillay, Onne Ronda, Ai‐Ching Boon, Evan Pennell, Kevin J. Ashton, Theo H. van Dijk, Karl‐Heinz Wagner, Henkjan J. Verkade, Andrew C. Bulmer

J Physiol. 2022 Apr 15; 600(8): 1889–1911. Published online 2022 Mar 1. doi: 10.1113/JP282395

PMCID:: PMC9310728

Article PDF–1.9M

Select item 92669499.

Beneficial and Detrimental Roles of Heme Oxygenase-1 in the Neurovascular System

Yoon Kyung Choi, Young-Myeong Kim

Int J Mol Sci. 2022 Jul; 23(13): 7041. Published online 2022 Jun 24. doi: 10.3390/ijms23137041

PMCID:: PMC9266949

Article PDF–1.0M

Select item 926660110.

Genetic testing of UGT1A1 in the diagnosis of Gilbert syndrome: The discovery of seven novel variants in the Chinese population

Leilei Gu, Yue Han, Donghua Zhang, Qiming Gong, Xinxin Zhang

Mol Genet Genomic Med. 2022 Jul; 10(7): e1958. Published online 2022 Apr 14. doi: 10.1002/mgg3.1958

PMCID:: PMC9266601

Article PDF–453K

Select item 901463311.

Gilbert or Crigler–Najjar syndrome? Neonatal severe unconjugated hyperbilirubinemia with P364L UGT1A1 homozygosity

Laura Cozzi, Federica Nuti, Irene Degrassi, Daniela Civeriati, Giulia Paolella, Gabriella Nebbia

Ital J Pediatr. 2022; 48: 59. Published online 2022 Apr 18. doi: 10.1186/s13052-022-01251-4

PMCID:: PMC9014633

Article PDF–1.0M

Select item 880080912.

UGT1A1基因复合杂合突变致吉尔伯特综合征一例

Weijie OU, Su LIN, Yilong WU, Yueyong ZHU

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2020 Jun 25; 49(3): 406–409. Chinese. doi: 10.3785/j.issn.1008-9292.2020.04.13

PMCID:: PMC8800809

Article PDF–1.8M

Select item 848189313.

Gilbert’s Syndrome and the Gut Microbiota – Insights From the Case-Control BILIHEALTH Study

Patrick A. Zöhrer, Claudia A. Hana, Nazlisadat Seyed Khoei, Christine Mölzer, Marlies Hörmann-Wallner, Anela Tosevska, Daniel Doberer, Rodrig Marculescu, Andrew C. Bulmer, Craig W. Herbold, David Berry, Karl-Heinz Wagner

Front Cell Infect Microbiol. 2021; 11: 701109. Published online 2021 Sep 16. doi: 10.3389/fcimb.2021.701109

PMCID:: PMC8481893

Article PDF–2.7M

Select item 791332714.

Genetic spectrum and clinical early natural history of glucose-6-phosphate dehydrogenase deficiency in Mexican children detected through newborn screening

Marcela Vela-Amieva, Miguel Angel Alcántara-Ortigoza, Ariadna González-del Angel, Leticia Belmont-Martínez, Carlos López-Candiani, Isabel Ibarra-González

Orphanet J Rare Dis. 2021; 16: 103. Published online 2021 Feb 26. doi: 10.1186/s13023-021-01693-9

PMCID:: PMC7913327

Article PDF–1.0M

Select item 744346515.

The coffee ingredients caffeic acid and caffeic acid phenylethyl ester protect against irinotecan‐induced leukopenia and oxidative stress response

Sandra Kalthoff, Stefan Paulusch, Alexander Rupp, Stefan Holdenrieder, Gunther Hartmann, Christian P. Strassburg

Br J Pharmacol. 2020 Sep; 177(18): 4193–4208. Published online 2020 Jul 16. doi: 10.1111/bph.15162

PMCID:: PMC7443465

Article PDF–3.1M

Select item 739012216.

反复皮肤、巩膜黄染2年

袁小叶, 贺湘玲, 邹惠, 邹润英

Zhongguo Dang Dai Er Ke Za Zhi. 2017 Jan 25; 19(1): 77–80. Chinese. doi: 10.7499/j.issn.1008-8830.2017.01.013

PMCID:: PMC7390122

Article PDF–1.1M

Select item 725092817.

A Gilbert syndrome-associated haplotype protects against fatty liver disease in humanized transgenic mice

Steffen Landerer, Sandra Kalthoff, Stefan Paulusch, Christian P. Strassburg

Sci Rep. 2020; 10: 8689. Published online 2020 May 26. doi: 10.1038/s41598-020-65481-4

PMCID:: PMC7250928

Article PDF–3.1M

Select item 669934518.

Analysis of the UGT1A1 Genotype in Hyperbilirubinemia Patients: Differences in Allele Frequency and Distribution

Xiao-xiao Mi, Jian Yan, Xiao-jie Ma, Ge-li Zhu, Yi-dan Gao, Wen-jun Yang, Xiao-wen Kong, Gong-ying Chen, Jun-ping Shi, Ling Gong

Biomed Res Int. 2019; 2019: 6272174. Published online 2019 Jul 29. doi: 10.1155/2019/6272174

PMCID:: PMC6699345

Article PDF–1.2M

Select item 636070419.

The frequency, clinical course, and health related quality of life in adults with Gilbert’s syndrome: a longitudinal study

Sanaa Kamal, Sara Abdelhakam, Dalia Ghoraba, Yasmin Massoud, Kareem Abdel Aziz, Huda Hassan, Tamer Hafez, Ahmed Abdel Sallam

BMC Gastroenterol. 2019; 19: 22. Published online 2019 Feb 4. doi: 10.1186/s12876-019-0931-2

PMCID:: PMC6360704

Article PDF–1.4M

Select item 631057520.

UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children: A retrospective analysis and quantitative correlation

Kuerbanjiang Abuduxikuer, Ling-Juan Fang, Li-Ting Li, Jing-Yu Gong, Jian-She Wang

Medicine (Baltimore) 2018 Dec; 97(49): e13576. Published online 2018 Dec 10. doi: 10.1097/MD.0000000000013576

PMCID:: PMC6310575

Article PDF–650K

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