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Jun 21, 2015 (publication date) through Apr 13, 2025
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Publication Name
World Journal of Gastroenterology
ISSN
1007-9327
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Zhang MH, Gong JY, Wang JS. Citrin deficiency presenting as acute liver failure in an eight-month-old infant. World J Gastroenterol 2015; 21(23): 7331-7334 [PMID: 26109823 DOI: 10.3748/wjg.v21.i23.7331] |
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| URL: | https://www.wjgnet.com/1007-9327/full/v21/i23/7331.htm |
| Number | Citing Articles |
| 1 |
Ting Zhang, Shasha Zhu, Haixia Miao, Jianbin Yang, Yezhen Shi, Yuwei Yue, Yu Zhang, Rulai Yang, Benqing Wu, Xinwen Huang. Dynamic changes of metabolic characteristics in neonatal intrahepatic cholestasis caused by citrin deficiency. Frontiers in Molecular Biosciences 2022; 9 doi: 10.3389/fmolb.2022.939837
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| 2 |
Chun-ting Lu, Ze-jian Li, Lie Feng, Jiong Li. Hepatic cirrhosis in a citrin-deficient infant. 2016 Sixth International Conference on Information Science and Technology (ICIST) 2016; : 14 doi: 10.1109/ICIST.2016.7483377
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| 3 |
Chun-Ting Lu, Qi-Ping Shi, Ze-Jian Li, Jiong Li, Lie Feng. Blood glucose and insulin and correlation of SLC25A13 mutations with biochemical changes in NICCD patients. Experimental Biology and Medicine 2017; 242(12): 1271 doi: 10.1177/1535370217710918
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| 4 |
Jiayi He, Jianling Zhang, Xuesong Li, Hong Wang, Cui Feng, Feng Fang, Sainan Shu. A Case Report: Can Citrin Deficiency Lead to Hepatocellular Carcinoma in Children?. Frontiers in Pediatrics 2019; 7 doi: 10.3389/fped.2019.00371
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| 5 |
Jun Kido, Georgios Makris, Saikat Santra, Johannes Häberle. Clinical landscape of citrin deficiency: A global perspective on a multifaceted condition. Journal of Inherited Metabolic Disease 2024; 47(6): 1144 doi: 10.1002/jimd.12722
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| 6 |
Robert Hegarty, Richard J. Thompson. Genetic aetiologies of acute liver failure. Journal of Inherited Metabolic Disease 2024; 47(4): 582 doi: 10.1002/jimd.12733
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| 7 |
Akella Radha Rama Devi, Shaik Mohammad Naushad. SLC25A13 c.1610_1612delinsAT mutation in an Indian patient and literature review of 79 cases of citrin deficiency for genotype-phenotype associations. Gene 2018; 668: 190 doi: 10.1016/j.gene.2018.05.076
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| 8 |
Toby Chun Hei Chan, Chloe Miu Mak, Matthew Chun Wing Yeung, Eric Chun-Yiu Law, Jana Cheung, Tsz Ki Wong, Vincent Wing-Sang Cheng, Jacky Kwan Ho Lee, Jimmy Chi Lap Wong, Cheuk Wing Fung, Kiran Moti Belaramani, Anne Mei Kwun Kwok, Kwok Yeung Tsang. Harnessing Next-Generation Sequencing as a Timely and Accurate Second-Tier Screening Test for Newborn Screening of Inborn Errors of Metabolism. International Journal of Neonatal Screening 2024; 10(1): 19 doi: 10.3390/ijns10010019
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| 9 |
S.C. Chong, P. Lo, C.W. Chow, L. Yuen, W.C.W. Chu, T.Y. Leung, J. Hui, F. Scaglia. Molecular and clinical characterization of citrin deficiency in a cohort of Chinese patients in Hong Kong. Molecular Genetics and Metabolism Reports 2018; 17: 3 doi: 10.1016/j.ymgmr.2018.08.002
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| 10 |
Kena Wang, Biao Zou, Fan Chen, Jianling Zhang, Zhihua Huang, Sainan Shu. Case report: Three novel variants on SLC25A13 in four infants with neonatal intrahepatic cholestasis caused by citrin deficiency. Frontiers in Pediatrics 2023; 11 doi: 10.3389/fped.2023.1103877
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| 11 |
Neng-Li Wang, Yi Lu, Jing-Yu Gong, Xin-Bao Xie, Jing Lin, Kuerbanjiang Abuduxikuer, Mei-Hong Zhang, Jian-She Wang. Molecular findings in children with inherited intrahepatic cholestasis. Pediatric Research 2020; 87(1): 112 doi: 10.1038/s41390-019-0548-8
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| 12 |
Yoshiyuki Okano, Toshihiro Ohura, Osamu Sakamoto, Ayano Inui. Current treatment for citrin deficiency during NICCD and adaptation/compensation stages: Strategy to prevent CTLN2. Molecular Genetics and Metabolism 2019; 127(3): 175 doi: 10.1016/j.ymgme.2019.06.004
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| 13 |
Xiao-Qi Sheng, Yi-Chao Wang. Novel two-step derivation method for the synchronous analysis of inherited metabolic disorders using urine. Experimental and Therapeutic Medicine 2017; 13(5): 1961 doi: 10.3892/etm.2017.4167
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| 14 |
Kuerbanjiang Abuduxikuer, Rui Chen, Zhong-Lin Wang, Jian-She Wang. Risk factors associated with mortality in neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) and clinical implications. BMC Pediatrics 2019; 19(1) doi: 10.1186/s12887-018-1383-5
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| 15 |
Michiharu Komatsu, Naoki Tanaka, Takefumi Kimura, Masahide Yazaki. Citrin Deficiency: Clinical and Nutritional Features. Nutrients 2023; 15(10): 2284 doi: 10.3390/nu15102284
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| 16 |
Lorena Fernández Tomé, Luiz Guilherme Stark Aroeira, Gema Muñoz Bartolo, Angela de la Vega Bueno, Carmen Camarena Grande, Esteban Frauca Remacha, Dolores Lledín Barbancho, María Alós Díez, María José Quiles Blanco, Laura Guerra, Manuel López Santamaría, Loreto Hierro Llanillo. Citrin deficiency: Early severe cases in a European country. Clinics and Research in Hepatology and Gastroenterology 2021; 45(4): 101595 doi: 10.1016/j.clinre.2020.101595
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| 17 |
Kiran Moti Belaramani, Toby Chun Hei Chan, Edgar Wai Lok Hau, Matthew Chun Wing Yeung, Anne Mei Kwun Kwok, Ivan Fai Man Lo, Terry Hiu Fung Law, Helen Wu, Sheila Suet Na Wong, Shirley Wai Lam, Gladys Ha Yin Ha, Toby Pui Yee Lau, Tsz Ki Wong, Venus Wai Ching Or, Rosanna Ming Sum Wong, Wong Lap Ming, Jasmine Chi Kwan Chow, Eric Kin Cheong Yau, Antony Fu, Josephine Shuk Ching Chong, Ho Chung Yau, Grace Wing Kit Poon, Kwok Leung Ng, Kwong Tat Chan, Yuen Yu Lam, Joannie Hui, Chloe Miu Mak, Cheuk Wing Fung. Expanded Newborn Screening for Inborn Errors of Metabolism in Hong Kong: Results and Outcome of a 7 Year Journey. International Journal of Neonatal Screening 2024; 10(1): 23 doi: 10.3390/ijns10010023
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| 18 |
Toni Vuković, Li Eon Kuek, Barbara Yu, Georgios Makris, Johannes Häberle. The therapeutic landscape of citrin deficiency. Journal of Inherited Metabolic Disease 2024; 47(6): 1157 doi: 10.1002/jimd.12768
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