For: | Vinayagamoorthy V, Srivastava A, Sarma MS. Newer variants of progressive familial intrahepatic cholestasis. World J Hepatol 2021; 13(12): 2024-2038 [PMID: 35070006 DOI: 10.4254/wjh.v13.i12.2024] |
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URL: | https://www.wjgnet.com/1007-9327/full/v13/i12/2024.htm |
Number | Citing Articles |
1 |
Angela Pepe, Angelo Colucci, Martina Carucci, Lucia Nazzaro, Cristina Bucci, Giusy Ranucci, Angelo Di Giorgio, Pietro Vajro, Claudia Mandato. Case Report: Add-on treatment with odevixibat in a new subtype of progressive familial intrahepatic cholestasis broadens the therapeutic horizon of genetic cholestasis. Frontiers in Pediatrics 2023; 11 doi: 10.3389/fped.2023.1061535
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2 |
Hana Halabi, Khawla Kalantan, Warif Abdulhaq, Habeib Alshaibi, Mohammed A Almatrafi. A Rare Case of Progressive Familial Intrahepatic Cholestasis Type 4: A Case Report and Literature Review. Cureus 2023; doi: 10.7759/cureus.47276
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3 |
Bikrant Bihari Lal, Seema Alam, Anupam Sibal, Karunesh Kumar, Somashekara Hosaagrahara Ramakrishna, Vaibhav Shah, Nirmala Dheivamani, Ashish Bavdekar, Aabha Nagral, Nishant Wadhwa, Arjun Maria, Aashay Shah, Ira Shah, Zahabiya Nalwalla, Pandey Snehavardhan, K.P. Srikanth, Subhash Gupta, Viswanathan M. Sivaramakrishnan, Yogesh Waikar, Arya Suchismita, A. Ashritha, Vikrant Sood, Rajeev Khanna. Genotype correlates with clinical course and outcome of children with tight junction protein 2 (TJP2) deficiency–related cholestasis. Hepatology 2024; 80(3): 511 doi: 10.1097/HEP.0000000000000828
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4 |
Mahintaj Dara, Negar Azarpira, Nasrin Motazedian, Mahdokht Hossein-Aghdaie, Seyed-Mohsen Dehghani, Bita Geramizadeh, Elaheh Esfandiari. Expression of miR-let7b and miR-19b in progressive familial intrahepatic cholestasis (PFIC) children. Gastroenterología y Hepatología (English Edition) 2024; 47(1): 24 doi: 10.1016/j.gastre.2023.03.003
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5 |
Angelo Di Giorgio, Marco Sciveres, Maurizio Fuoti, Aurelio Sonzogni, Claudia Mandato, Lorenzo D'Antiga. Treatment with an ileal bile acid transporter inhibitor in patients with TJP2 deficiency. Clinics and Research in Hepatology and Gastroenterology 2023; 47(8): 102185 doi: 10.1016/j.clinre.2023.102185
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6 |
Vipul Gautam, Kalpana Panda, Vikram Kumar, Shaleen Agarwal, Subhash Gupta. Youngest Living Donor Liver Transplant for End‐Stage Liver Disease in a 6‐Month‐Old With a Novel Aggressive Mutation in KIF12 Gene. Pediatric Transplantation 2024; 28(5) doi: 10.1111/petr.14804
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7 |
K. S. Nezhdanov, E. N. Shirokova, Yu. O. Shulpekova, A. S. Ostrovskaya, M. S. Zharkova, V. T. Ivashkin. A 19-year-old Patient with Recurrent Pruritus and Jaundice. Russian Journal of Gastroenterology, Hepatology, Coloproctology 2023; 33(3): 66 doi: 10.22416/1382-4376-2023-33-3-66-75
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8 |
Dalal Ben Sabbahia, Meriem Atrasssi, Nissrine Bennani, Abdelhakim Benmoussa, Abdelhak Abkari. ZFYVE19 gene mutation: A novel variant of progressive familial intrahepatic cholestasis. JPGN Reports 2024; doi: 10.1002/jpr3.12111
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9 |
Leilei Yu, Yaru Liu, Shunhe Wang, Qingsong Zhang, Jianxin Zhao, Hao Zhang, Arjan Narbad, Fengwei Tian, Qixiao Zhai, Wei Chen. Cholestasis: exploring the triangular relationship of gut microbiota-bile acid-cholestasis and the potential probiotic strategies. Gut Microbes 2023; 15(1) doi: 10.1080/19490976.2023.2181930
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10 |
Yue Zu, Yanan Liu, Lulu Lan, Chen Zhu, Chengliang Zhang, Dong Liu. Consecutive baicalin treatment relieves its accumulation in rats with intrahepatic cholestasis by increasing MRP2 expression. Heliyon 2023; 9(1): e12689 doi: 10.1016/j.heliyon.2022.e12689
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11 |
Maria Noelle Hüpper, Judith Pichler, Wolf-Dietrich Huber, Andreas Heilos, Rebecca Schaup, Martin Metzelder, Sophie Langer. Surgical versus Medical Management of Progressive Familial Intrahepatic Cholestasis—Case Compilation and Review of the Literature. Children 2023; 10(6): 949 doi: 10.3390/children10060949
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12 |
Mahintaj Dara, Negar Azarpira, Nasrin Motazedian, Mahdokht Hossein-Aghdaie, Seyed-Mohsen Dehghani, Bita Geramizadeh, Elaheh Esfandiari. Expression of miR-let7b and miR-19b in progressive familial intrahepatic cholestasis (PFIC) children. Gastroenterología y Hepatología 2024; 47(1): 24 doi: 10.1016/j.gastrohep.2023.03.001
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13 |
Rachel M. Golonka, Beng San Yeoh, Piu Saha, Amira Gohara, Ramakumar Tummala, Stanislaw Stepkowski, Amit K. Tiwari, Bina Joe, Frank J. Gonzalez, Andrew T. Gewirtz, Matam Vijay-Kumar. Loss of toll-like receptor 5 potentiates spontaneous hepatocarcinogenesis in farnesoid X receptor–deficient mice. Hepatology Communications 2023; 7(6) doi: 10.1097/HC9.0000000000000166
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14 |
Ikuo Tomioka, Chihiro Ota, Yuka Tanahashi, Kayoko Ikegami, Ayaka Ishihara, Nanami Kohri, Hiroshi Fujii, Kanako Morohaku. Loss of the DNA-binding domain of the farnesoid X receptor gene causes severe liver and kidney injuries. Biochemical and Biophysical Research Communications 2024; 721: 150125 doi: 10.1016/j.bbrc.2024.150125
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15 |
Harry Sutton, Saul J. Karpen, Binita M. Kamath. Pediatric Cholestatic Diseases: Common and Unique Pathogenic Mechanisms. Annual Review of Pathology: Mechanisms of Disease 2024; 19(1): 319 doi: 10.1146/annurev-pathmechdis-031521-025623
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16 |
Deanna M. Bowman, Izumi Kaji, James R. Goldenring. Altered MYO5B Function Underlies Microvillus Inclusion Disease: Opportunities for Intervention at a Cellular Level. Cellular and Molecular Gastroenterology and Hepatology 2022; 14(3): 553 doi: 10.1016/j.jcmgh.2022.04.015
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17 |
Tingting Lv, Jidong Jia. Rare liver diseases are not rare in China. Liver International 2022; 42(9): 2023 doi: 10.1111/liv.15267
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18 |
Nicole Heinz, Jennifer Vittorio. Treatment of Cholestasis in Infants and Young Children. Current Gastroenterology Reports 2023; 25(11): 344 doi: 10.1007/s11894-023-00891-8
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19 |
Binbin Liu, Jie Zhang, Lu Shao, Jiaming Yao, Shuli Yang. San-Huang-Chai-Zhu Formula Ameliorates Liver Injury in Intrahepatic Cholestasis through Suppressing SIRT1/PGC-1α-Regulated Mitochondrial Oxidative Stress. Evidence-Based Complementary and Alternative Medicine 2022; 2022: 1 doi: 10.1155/2022/7832540
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20 |
Chiao‐Yu Yang, Hung‐Wen Tsai, Yen‐Yin Chou, Yao‐Jong Yang. NR1H4 mutation and rapid progressive intrahepatic cholestasis in infancy: A case report and literature review. Clinical Case Reports 2024; 12(2) doi: 10.1002/ccr3.8531
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21 |
Arghya Samanta, Neha Parveen, Moinak Sen Sarma, Ujjal Poddar, Anshu Srivastava. Cholestatic Liver Disease due to Novel USP53 Mutations: A Case Series of Three Indian Children. Journal of Clinical and Experimental Hepatology 2024; 14(2): 101290 doi: 10.1016/j.jceh.2023.10.001
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22 |
Joanna Głowska-Ciemny, Marcin Szymanski, Agata Kuszerska, Rafał Rzepka, Constantin S. von Kaisenberg, Rafał Kocyłowski. Role of Alpha-Fetoprotein (AFP) in Diagnosing Childhood Cancers and Genetic-Related Chronic Diseases. Cancers 2023; 15(17): 4302 doi: 10.3390/cancers15174302
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23 |
T. N. Belkova, E. B. Pavlinova, K. B. Kurieva, Yu. E. Golovanova, A. Yu. Konstantinova, A. Kh. Begjanova. A case report of progressive familial intrahepatic cholestasis in neonatal practice. Meditsinskiy sovet = Medical Council 2024; (11): 306 doi: 10.21518/ms2024-216
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24 |
Guillaume Morcrette, Monique Fabre. Biopsie hépatique dans la prise en charge des cholestases de l’enfant. Revue Francophone des Laboratoires 2023; 2022(548): 60 doi: 10.1016/S1773-035X(22)00405-1
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25 |
Dr Moinak Sen Sarma, Chiranjit Gope. Approach to a Sick Neonate with Cholestasis in India. Annals of Pediatric Gastroenterology & Hepatology 2022; 4(2): 6 doi: 10.5005/jp-journals-11009-0094
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