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May 27, 2019 (publication date) through Apr 30, 2024
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Publication Name
World Journal of Hepatology
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1948-5182
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Henkel SA, Squires JH, Ayers M, Ganoza A, Mckiernan P, Squires JE. Expanding etiology of progressive familial intrahepatic cholestasis. World J Hepatol 2019; 11(5): 450-463 [PMID: 31183005 DOI: 10.4254/wjh.v11.i5.450] |
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| URL: | https://www.wjgnet.com/1948-5182/full/v11/i5/450.htm |
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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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| 15 |
Burcu GÜVEN. ÇOCUKLARDA KRONİK KARACİĞER HASTALIKLARINA YAKLAŞIM. Kırıkkale Üniversitesi Tıp Fakültesi Dergisi 2020; 22(1): 121 doi: 10.24938/kutfd.692278
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Huayu Chen, Dongbo Wu, Wei Jiang, Ting Lei, Changli Lu, Taoyou Zhou. Case Report: A Novel Homozygous Variant Identified in a Chinese Patient With Benign Recurrent Intrahepatic Cholestasis-Type 1. Frontiers in Medicine 2021; 8 doi: 10.3389/fmed.2021.705489
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Beatriz Mínguez Rodríguez, Cristina Molera Busoms, Loreto Martorell Sampol, Ruth García Romero, Gemma Colomé Rivero, Javier Martín de Carpi. Heterozygous mutations of ATP8B1, ABCB11 and ABCB4 cause mild forms of Progressive Familial Intrahepatic Cholestasis in a pediatric cohort. Gastroenterología y Hepatología (English Edition) 2022; 45(8): 585 doi: 10.1016/j.gastre.2021.12.004
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| 18 |
Patrick J. McKiernan, James E. Squires, Robert H. Squires, Jerry Vockley, George V. Mazariegos, Kyle Soltys, Armando Ganoza, Kevin Strauss, Ajai Khanna, Rakesh Sindhi. Liver transplant for inherited metabolic disease among siblings. Clinical Transplantation 2020; 34(11) doi: 10.1111/ctr.14090
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| 19 |
Johanna M. Ascher Bartlett, Jay Shah. Benign Hematologic Disorders in Children. 2021; : 353 doi: 10.1007/978-3-030-49980-8_24
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Adriana C. Norris, Alexander J. Mansueto, Mariana Jimenez, Eugenia M. Yazlovitskaya, Bhawik K. Jain, Todd R. Graham. Flipping the script: Advances in understanding how and why P4-ATPases flip lipid across membranes. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research 2024; 1871(4): 119700 doi: 10.1016/j.bbamcr.2024.119700
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| 21 |
Mazen Noureddin, Suntje Sander-Struckmeier, José M Mato. Early treatment efficacy of S-adenosylmethionine in patients with intrahepatic cholestasis: A systematic review. World Journal of Hepatology 2020; 12(2): 46-63 doi: 10.4254/wjh.v12.i2.46
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Gaël A. Kornitzer, Fernando Alvarez. Case Report: A Novel Single Variant TJP2 Mutation in a Case of Benign Recurrent Intrahepatic Cholestasis. JPGN Reports 2021; 2(3): e087 doi: 10.1097/PG9.0000000000000087
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| 23 |
Seema Alam, Bikrant Bihari Lal. Recent updates on progressive familial intrahepatic cholestasis types 1, 2 and 3: Outcome and therapeutic strategies. World Journal of Hepatology 2022; 14(1): 98-118 doi: 10.4254/wjh.v14.i1.98
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Beatriz Mínguez Rodríguez, Cristina Molera Busoms, Loreto Martorell Sampol, Ruth García Romero, Gemma Colomé Rivero, Javier Martín de Carpi. Heterozygous mutations of ATP8B1, ABCB11 and ABCB4 cause mild forms of Progressive Familial Intrahepatic Cholestasis in a pediatric cohort. Gastroenterología y Hepatología 2022; 45(8): 585 doi: 10.1016/j.gastrohep.2021.12.005
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Stanisław M. Jurk, Andreas E. Kremer, Ekkehard Schleussner. Intrahepatic Cholestasis of Pregnancy. Geburtshilfe und Frauenheilkunde 2021; 81(08): 940 doi: 10.1055/a-1522-5178
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Fatma İlknur Varol, Mukadder Ayşe Selimoğlu, Şükrü Güngör, Sezai Yılmaz, İbrahim Tekedereli. Single-center experience in management of progressive familial intrahepatic cholestasis. Arab Journal of Gastroenterology 2021; 22(4): 310 doi: 10.1016/j.ajg.2021.05.021
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Mariano Piazzolla, Nicola Castellaneta, Antonio Novelli, Emanuele Agolini, Dario Cocciadiferro, Leonardo Resta, Loren Duda, Michele Barone, Enzo Ierardi, Alfredo Di Leo. Nonsense variant of <i>ATP8B1</i> gene in heterozygosis and benign recurrent intrahepatic cholestasis: A case report and review of literature. World Journal of Hepatology 2020; 12(2): 64-71 doi: 10.4254/wjh.v12.i2.64
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Nihal Uyar Aksu, Orhan Görükmez, Özlem Görükmez, Ayşen Uncuoğlu. A Novel Homozygous Mutation in the MYO5B Gene Associated With Normal-Gamma-Glutamyl Transferase Progressive Familial Intrahepatic Cholestasis. Cureus 2021; doi: 10.7759/cureus.19326
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Sophia Giang, Ruth Lillian Gordon, Kelly B. Haas. A Diagnostic Quagmire: PFIC5 Presenting as a Rare Cause of Neonatal Cholestasis. ACG Case Reports Journal 2021; 8(4): e00558 doi: 10.14309/crj.0000000000000558
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