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Items: 1 to 20 of 44

1.
Perioperative Management of Patient with Esophageal Carcinoma and Crigler-Najjar Syndrome Type 2: A Case Report
Dehua Ma, Fang Chen, Xiaoyun Chen, Yu Chen
Front Surg. 2022; 9: 889753. Published online 2022 Apr 27. doi: 10.3389/fsurg.2022.889753
PMCID:
PMC9093071
ArticlePubReaderPDF–905KCite
2.
Crigler Najjar Syndrome Type 2 (CNS Type 2): An Unwonted Cause of Jaundice in Adults
Prabhat Kumar, Gargi Sasmal, Shreya Gupta, Renu Saxena, Sudha Kohli
J Clin Diagn Res. 2017 Jul; 11(7): OD05–OD06. Published online 2017 Jul 1. doi: 10.7860/JCDR/2017/28195.10221
PMCID:
PMC5583863
ArticlePubReaderPDF–163KCite
3.
Management of pregnancy in Crigler Najjar syndrome type 2
Alisha Nitin Chaubal, Ruchir Patel, Dhaval Choksi, Kaivan Shah, Meghraj Ingle, Prabha Sawant
World J Hepatol. 2016 Apr 18; 8(11): 530–532. Published online 2016 Apr 18. doi: 10.4254/wjh.v8.i11.530
PMCID:
PMC4832095
ArticlePubReaderPDF–786KCite
4.
Crigler-Najjar syndrome type 2: Novel UGT1A1 mutation
Karippoth Mohandas Nair, Peter Lohse, Sheela Nampoothiri
Indian J Hum Genet. 2012 May-Aug; 18(2): 233–234. doi: 10.4103/0971-6866.100776
PMCID:
PMC3491300
ArticlePubReaderPDF–137KCite
5.
Case report: A rare case of pyruvate kinase deficiency and Crigler-Najjar syndrome type II with a novel pathogenic variant of PKLR and UGT1A1 mutation
Huan Wu, Long Wu, Quan Zhang, Bao-fang Zhang
Front Genet. 2023; 14: 1229271. Published online 2023 Aug 21. doi: 10.3389/fgene.2023.1229271
PMCID:
PMC10475990
ArticlePubReaderPDF–1.1MCite
6.
Novel UGT1A1 Gene Mutations in a Boy with Crigler–Najjar Syndrome Type II
David Pérez-Solís, Bárbara Montes-Zapico, Ana-Cristina Rodríguez-Dehli, María García-Hoyos, Mireia Arroyo-Hernández
J Pediatr Genet. 2021 Dec; 10(4): 323–325. Published online 2020 Jul 29. doi: 10.1055/s-0040-1714361
PMCID:
PMC8608478
ArticlePubReaderPDF–147KCite
7.
A Rare Case Report of Crigler Najjar Syndrome Type II
Eusha Abdul Raffay, Ayesha Liaqat, Maria Khan, Ali I Awan, Bakhat Mand
Cureus. 2021 Jan; 13(1): e12669. Published online 2021 Jan 12. doi: 10.7759/cureus.12669
PMCID:
PMC7880822
ArticlePubReaderPDF–79KCite
8.
p.Cys223Tyr mutation causing Crigler–Najjar syndrome type II
Qing‐Fang Xiong, Hui Zhou, Yong‐Feng Yang
JGH Open. 2020 Oct; 4(5): 1009–1011. Published online 2020 May 16. doi: 10.1002/jgh3.12355
PMCID:
PMC7578310
ArticlePubReaderPDF–850KCite
9.
Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II
Lei Sun, Man Li, Liang Zhang, Xiaoying Teng, Xiangmei Chen, Xingang Zhou, Zhiyuan Ma, Liming Qi, Peng Wang
Medicine (Baltimore) 2017 Nov; 96(45): e8620. Published online 2017 Nov 10. doi: 10.1097/MD.0000000000008620
PMCID:
PMC5690788
ArticlePubReaderPDF–297KCite
10.
Reduction of hyperbilirubinemia with hypericum extract (St. John's Wort) in a patient with Crigler‐Najjar syndrome type II
Oliver Kummer, Felix Hammann, Manuel Haschke, Stephan Krähenbühl
Br J Clin Pharmacol. 2016 May; 81(5): 1002–1004. Published online 2016 Mar 7. doi: 10.1111/bcp.12869
PMCID:
PMC4834607
ArticlePubReaderPDF–180KCite
11.
Acute cholangitis in an old patient with Crigler-Najjar syndrome type II - a case report
Samuel Raimundo Fernandes, Carlos Miguel Moura, Beatriz Rodrigues, Luís Araújo Correia, Helena Cortez-Pinto, José Velosa
BMC Gastroenterol. 2016; 16: 33. Published online 2016 Mar 11. doi: 10.1186/s12876-016-0449-9
PMCID:
PMC4788912
ArticlePubReaderPDF–1.0MCite
12.
Spectrum of UGT1A1 Variations in Chinese Patients with Crigler-Najjar Syndrome Type II
Lufeng Li, Guohong Deng, Yi Tang, Qing Mao
PLoS One. 2015; 10(5): e0126263. Published online 2015 May 20. doi: 10.1371/journal.pone.0126263
PMCID:
PMC4439166
ArticlePubReaderPDF–556KCite
13.
Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5′-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis
Bixia Zheng, Guorui Hu, Jin Yu, Zhifeng Liu
BMC Pediatr. 2014; 14: 267. Published online 2014 Oct 15. doi: 10.1186/1471-2431-14-267
PMCID:
PMC4287334
ArticlePubReaderPDF–248KCite
14.
Molecular Analysis of the UGT1A1 Gene in Korean Patients with Crigler-Najjar Syndrome Type II
Jae Sung Ko, Ju Young Chang, Jin Soo Moon, Hye Ran Yang, Jeong Kee Seo
Pediatr Gastroenterol Hepatol Nutr. 2014 Mar; 17(1): 37–40. Published online 2014 Mar 31. doi: 10.5223/pghn.2014.17.1.37
PMCID:
PMC3990781
ArticlePubReaderPDF–308KCite
15.
Truncated UDP-glucuronosyltransferase (UGT) from a Crigler–Najjar syndrome type II patient colocalizes with intact UGT in the endoplasmic reticulum
Masahiro Suzuki, Marie Hirata, Miho Takagi, Taiichi Watanabe, Tomohiro Iguchi, Kotaro Koiwai, So Maezawa, Osamu Koiwai
J Hum Genet. 2014 Mar; 59(3): 158–162. Published online 2014 Jan 9. doi: 10.1038/jhg.2013.138
PMCID:
PMC3973126
ArticlePubReaderPDF–775KCite
16.
Mutation Analysis in Crigler-Najjar Syndrome Type II—Case Report and Literature Review
Piyush Ranjan, Sudha Kohli, Renu Saxena, Seema Thakur
J Clin Exp Hepatol. 2011 Dec; 1(3): 204–206. Published online 2012 Jan 2. doi: 10.1016/S0973-6883(11)60239-9
PMCID:
PMC3940311
SummaryPDF–98KCite
17.
Hereditary Spherocytosis Coexisting with UDP-Glucuronosyltransferase Deficiency Highly Suggestive of Crigler-Najjar Syndrome Type II
Shigeo Iijima, Takehiko Ohzeki, Yoshihiro Maruo
Yonsei Med J. 2011 Mar 1; 52(2): 369–372. Published online 2011 Jan 29. doi: 10.3349/ymj.2011.52.2.369
PMCID:
PMC3051216
ArticlePubReaderPDF–280KCite
18.
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
ArticlePubReaderPDF–1.0MCite
19.
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
ArticlePubReaderPDF–650KCite
20.
Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome
Linda Gailite, Dmitrijs Rots, Ieva Pukite, Gunta Cernevska, Madara Kreile
BMC Pediatr. 2018; 18: 317. Published online 2018 Oct 3. doi: 10.1186/s12887-018-1285-6
PMCID:
PMC6169020
ArticlePubReaderPDF–719KCite

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