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Feb 21, 2019 (publication date) through Apr 25, 2024
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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, Setchell KD, Zhao J, Gong JY, Lu Y, Wang JS. Δ4-3-oxosteroid-5β-reductase deficiency: Responses to oral bile acid therapy and long-term outcomes. World J Gastroenterol 2019; 25(7): 859-869 [PMID: 30809085 DOI: 10.3748/wjg.v25.i7.859] |
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| URL: | https://www.wjgnet.com/1007-9327/full/v25/i7/859.htm |
| Number | Citing Articles |
| 1 |
Jing Zhao, Yi-Ling Qiu, Li Wang, Zhong-Die Li, Xin-Bao Xie, Yi Lu, Kenneth D.R. Setchell, Ye Cheng, Qing-He Xing, Jian-She Wang. Recurrent AKR1D1 c.580-13T>A Variant. The Journal of Molecular Diagnostics 2023; 25(4): 227 doi: 10.1016/j.jmoldx.2023.01.004
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| 2 |
Akihiko Kimura, Tatsuki Mizuochi, Hajime Takei, Akira Ohtake, Jun Mori, Kunihiro Shinoda, Takuji Hashimoto, Mureo Kasahara, Takao Togawa, Tsuyoshi Murai, Takashi Iida, Hiroshi Nittono. Bile Acid Synthesis Disorders in Japan: Long-Term Outcome and Chenodeoxycholic Acid Treatment. Digestive Diseases and Sciences 2021; 66(11): 3885 doi: 10.1007/s10620-020-06722-4
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| 3 |
Antoine Gardin, Mathias Ruiz, Jan Beime, Mara Cananzi, Margarete Rathert, Barbara Rohmer, Enke Grabhorn, Marion Almes, Veena Logarajah, Luis Peña-Quintana, Thomas Casswall, Amaria Darmellah-Remil, Ana Reyes-Domínguez, Emna Barkaoui, Loreto Hierro, Carolina Baquero-Montoya, Ulrich Baumann, Björn Fischler, Emmanuel Gonzales, Anne Davit-Spraul, Sophie Laplanche, Emmanuel Jacquemin. ∆4-3-oxo-5β-reductase deficiency: favorable outcome in 16 patients treated with cholic acid. Orphanet Journal of Rare Diseases 2023; 18(1) doi: 10.1186/s13023-023-02984-z
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| 4 |
Frans Stellaard, Dieter Lütjohann. Dynamics of the enterohepatic circulation of bile acids in healthy humans. American Journal of Physiology-Gastrointestinal and Liver Physiology 2021; 321(1): G55 doi: 10.1152/ajpgi.00476.2020
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| 5 |
Anh-Hoa Nguyen Pham, Kim-Oanh Bui Thi, Mai-Huong Nguyen Thi, Diem-Ngoc Ngo, Nakayuki Naritaka, Hiroshi Nittono, Hisamitsu Hayashi, Trang Thi Dao, Kim-Huong Thi Nguyen, Hoai-Nghia Nguyen, Hoa Giang, Hung-Sang Tang, Tat-Thanh Nguyen, Dinh-Kiet Truong, Minh-Dien Tran. Clinical and genetic features of congenital bile acid synthesis defect with a novel mutation in AKR1D1 gene sequencing. Medicine 2022; 101(25): e29476 doi: 10.1097/MD.0000000000029476
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| 6 |
Kenneth D.R. Setchell, James E. Heubi. Liver Disease in Children. 2021; : 593 doi: 10.1017/9781108918978.033
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Rune Rose Tronstad, Siren Berland, Erling Tjora, Khadija El Jellas, Ingvild Aukrust, Kurt Kristensen, Dag Tveitnes, Anders Molven, Hanns-Ulrich Marschall, Anuradha Rao, Paul A. Dawson. Fat Malabsorption and Ursodeoxycholic Acid Treatment in Children With Reduced Organic Solute Transporter-α (SLC51A) Expression. JPGN Reports 2022; 3(3): e229 doi: 10.1097/PG9.0000000000000229
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Akihiko Kimura, Jun Mori, Anh-Hoa Nguyen Pham, Kim-Oanh Bui Thi, Hajime Takei, Tsuyoshi Murai, Hisamitsu Hayashi, Hiroshi Nittono. Healthy Patients With AKR1D1 Mutation Not Requiring Primary Bile Acid Therapy: A Case Series. JPGN Reports 2023; 4(4): e372 doi: 10.1097/PG9.0000000000000372
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