For: | Shah R, Taborda C, Chawla S. Acute and chronic hepatobiliary manifestations of sickle cell disease: A review. World J Gastrointest Pathophysiol 2017; 8(3): 108-116 [PMID: 28868180 DOI: 10.4291/wjgp.v8.i3.108] |
---|---|
URL: | https://www.wjgnet.com/2150-5330/full/v8/i3/108.htm |
Number | Citing Articles |
1 |
Valéria de Freitas Dutra, Thais Priscila Biassi, Maria Stella Figueiredo. Sickle cell anemia: hierarchical cluster analysis and clinical profile in a cohort in Brazil. Hematology, Transfusion and Cell Therapy 2023; 45(1): 45 doi: 10.1016/j.htct.2021.08.015
|
2 |
Eirini Kyrana, David Rees, Florence Lacaille, Emer Fitzpatrick, Mark Davenport, Nigel Heaton, Sue Height, Marianne Samyn, Fulvio Mavilio, Valentine Brousse, Abid Suddle, Subarna Chakravorty, Anita Verma, Girish Gupte, Marki Velangi, Baba Inusa, Emma Drasar, Nedim Hadzic, Tassos Grammatikopoulos, Jonathan Hind, Maesha Deheragoda, Maria Sellars, Anil Dhawan. Clinical management of sickle cell liver disease in children and young adults. Archives of Disease in Childhood 2021; 106(4): 315 doi: 10.1136/archdischild-2020-319778
|
3 |
Bahareh Moghimian Boroujeni, Mehran Varnaseri Ghandali, Najmadin Saki, Alireza Ekrami, Aram Asareh Zadegan Dezfuli, Arshid Yousefi-Avarvand. Mini review Salmonella: A problem in patients with sickle cell anemia. Gene Reports 2021; 23: 101118 doi: 10.1016/j.genrep.2021.101118
|
4 |
Prabir Maji, Rohan Malik. Acute Liver Failure in a Sickle Cell Patient. Journal of Pediatric Gastroenterology and Nutrition 2021; 73(1) doi: 10.1097/MPG.0000000000003141
|
5 |
Nicholas B Burley, Kenneth D Miller. Acute Liver Failure in Sickle Cell Disease: A Perfect Storm. Cureus 2021; doi: 10.7759/cureus.15680
|
6 |
Aditi Kumar, Rashmi Ranjan Behera, Samarendra Mahapatro, Ranjan Patel, Hemanta Nayak, Amit Kumar Satapathy. Paediatric sickle cell disease presenting with hepatobiliary symptoms—a case presentation and brief literature review. Egyptian Pediatric Association Gazette 2024; 72(1) doi: 10.1186/s43054-024-00288-w
|
7 |
Denis Soulières, Jules Mercier-Ross, Caroline Fradette, Anna Rozova, Yu Chung Tsang, Fernando Tricta. The pharmacokinetic and safety profile of single-dose deferiprone in subjects with sickle cell disease. Annals of Hematology 2022; 101(3): 533 doi: 10.1007/s00277-021-04728-0
|
8 |
Harsha Lad, Shoma Naskar, S. K. D. B. Punyasri Pasupuleti, Rakesh Nahrel, Pradeep Sihare, Giriraj R. Chandak, Pradeep K. Patra. Evaluation of pharmacological efficacy and safety of hydroxyurea in sickle cell disease: Study of a pediatric cohort from Chhattisgarh, India. Pediatric Hematology and Oncology 2023; 40(4): 395 doi: 10.1080/08880018.2022.2126042
|
9 |
Thiago Trovati Maciel, Rachel Rignault, Slimane Allali, Olivier Hermine. Current Practices in Sickle Cell Disease. 2024; doi: 10.5772/intechopen.1005751
|
10 |
Yamini Sundara Priya Dasiah, Martina Saeid, Fatmaelzahraa Ahmed . Intrahepatic Cholestasis in a Pregnant Patient With Sickle Cell Disease: A Case Report. Cureus 2024; doi: 10.7759/cureus.60611
|
11 |
Ugochi O Ogu, Nnenna U Badamosi, Pamela E Camacho, Amado X Freire, Patricia Adams-Graves. Management of Sickle Cell Disease Complications Beyond Acute Chest Syndrome. Journal of Blood Medicine 2021; : 101 doi: 10.2147/JBM.S291394
|
12 |
Orith Waisbourd-Zinman, Rachel Frenklak, Odelia Hakakian, Didja Hilmara, Henry Lin. Autoimmune Liver Disease in Patients With Sickle Cell Disease. Journal of Pediatric Hematology/Oncology 2021; 43(7): 254 doi: 10.1097/MPH.0000000000001985
|
13 |
L.V.K.S. Bhaskar, Smaranika Pattnaik. Association of Clinical and Hematological variables with the disease severity in Indian Sickle cell anemia patients. Research Journal of Pharmacy and Technology 2021; : 5254 doi: 10.52711/0974-360X.2021.00915
|
14 |
Slimane Allali, Mariane de Montalembert, Valentine Brousse, Claire Heilbronner, Melissa Taylor, Josephine Brice, Elisabetta Manzali, Nicolas Garcelon, Florence Lacaille. Hepatobiliary Complications in Children with Sickle Cell Disease: A Retrospective Review of Medical Records from 616 Patients. Journal of Clinical Medicine 2019; 8(9): 1481 doi: 10.3390/jcm8091481
|
15 |
Syed Ahsan Rizvi, Akash Pandey. Response to. Journal of Pediatric Gastroenterology and Nutrition 2021; 73(1) doi: 10.1097/MPG.0000000000003142
|
16 |
Ilknur Kozanoglu, Hakan Ozdogu. Use of red blood cell exchange for treating acute complications of sickle cell disease. Transfusion and Apheresis Science 2018; 57(1): 23 doi: 10.1016/j.transci.2018.02.011
|
17 |
Neha Wadhavkar, John Paul Nsubuga, Nouran Ibrahim, Prasanna Kumar, Andrew Hsu, Shannon Simmons. Acute Liver Failure With Liver Enzymes >5,000 in Sickle Cell Disease. ACG Case Reports Journal 2024; 11(3): e01303 doi: 10.14309/crj.0000000000001303
|
18 |
Melina J. Saavedra, Chellapriya Vythinathan, Ratna B. Basak, Siddharth Dubey, Stephan Kohlhoff, Ninad Desai. Prolonged Fever in a 3-Year-Old With Sickle Cell Disease. Pediatrics 2024; 153(5) doi: 10.1542/peds.2023-064274
|
19 |
Gifty Mawuli, Bartholomew Dzudzor, Kenneth Tachi, Amma Anima Benneh-Akwasi Kuma, James Odame-Aboagye, Billal Musah Obeng, Anthony Twumasi Boateng, Elijah Paa Edu-Quansah, Keren Okyerebea Attiku, Esinam Agbosu, Augustina Arjarquah, Joseph Humphrey Kofi Bonney. Hepatitis C virus (HCV) infection among patients with sickle cell disease at the Korle-Bu teaching hospital. Virology Journal 2022; 19(1) doi: 10.1186/s12985-022-01797-z
|
20 |
Leonardo Rodrigues de Oliveira, Ana Laura Castro Costa, Paula Veloso Almeida, Luzia Beatriz Ribeiro Zago, Vanessa Afonso da Silva, Sheila Soares-Silva. Dengue fever as a potential cause of sickle cell intrahepatic cholestasis: A report of two cases. Revista da Sociedade Brasileira de Medicina Tropical 2021; 54 doi: 10.1590/0037-8682-0010-2021
|
21 |
Rashmi Parikh, Nalini Bansal, Rajeev Sen. Liver histopathology in scope of hematological disorders. Indian Journal of Pathology and Microbiology 2023; 66(4): 683 doi: 10.4103/ijpm.ijpm_856_22
|
22 |
Masoumeh Jabarpour, Vahid Siavashi, Simin Asadian, Homa Babaei, Seyedeh Maedeh Jafari, Seyed Mahdi Nassiri. Hyperbilirubinemia-induced pro-angiogenic activity of infantile endothelial progenitor cells. Microvascular Research 2018; 118: 49 doi: 10.1016/j.mvr.2018.02.005
|
23 |
Morteza Hassanzadeh, Zahra Momayez Sanat, Somayeh Khayatian, Mohammadjavad Sotoudeheian, Amirmasoud Shahbazian, SeyedAhmad Hoseini. Acute sickle cell hepatopathy: A case report and literature review. Journal of the National Medical Association 2024; 116(2): 119 doi: 10.1016/j.jnma.2023.09.013
|
24 |
Abrar J. Alwaheed, Safi G. Alqatari, Dania M. AlKhafaji, Reem J. Al Argan, Osama A. Al Sultan, Reem S. AlSulaiman, Faisal S. AlShahrani, Faisal A. Alghamdi, Abdullah M. Alkhudair, Abdulrahman A. Alghamdi. Clinical outcome of pre-operative blood transfusion for sickle cell disease patients in post-operative complications. Hospital Practice 2022; 50(5): 361 doi: 10.1080/21548331.2022.2121574
|
25 |
Zafraan Zathar, Sunil James, Nickki Pressler, Emily Ho, Christian F Camm, Carlos Minguito Carazo, Peysh Patel. Constrictive pericarditis masquerading as hepatic sequestration crisis in a patient with sickle cell disease: a case report. European Heart Journal - Case Reports 2020; 4(1): 1 doi: 10.1093/ehjcr/ytaa006
|
26 |
Matthew D. Gosse, Dustin E. Bosch. Congestive Hepatopathy: A Case of Fontan-Associated Liver Disease and Review of Literature. AJSP: Reviews and Reports 2022; 27(6): 241 doi: 10.1097/PCR.0000000000000534
|
27 |
Dibya L. Praharaj, Anil C. Anand. Sickle Hepatopathy. Journal of Clinical and Experimental Hepatology 2021; 11(1): 82 doi: 10.1016/j.jceh.2020.08.003
|
28 |
Philipp Kasper, Frank Tacke, Hans-Michael Steffen, Guido Michels. Hepatische Dysfunktion bei Patienten mit kardiogenem Schock. Der Kardiologe 2020; 14(3): 229 doi: 10.1007/s12181-020-00404-1
|
29 |
Sayuri Kamimura, Meghann Smith, Sebastian Vogel, Luis E.F. Almeida, Swee Lay Thein, Zenaide M.N. Quezado. Mouse models of sickle cell disease: Imperfect and yet very informative. Blood Cells, Molecules, and Diseases 2024; 104: 102776 doi: 10.1016/j.bcmd.2023.102776
|
30 |
Carolina Mariano Pompeo, Andreia Insabralde de Queiroz Cardoso, Mercy da Costa Souza, Mayara Bontempo Ferraz, Marcos Antonio Ferreira Júnior, Maria Lúcia Ivo. Fatores de risco para mortalidade em pacientes com doença falciforme: uma revisão integrativa. Escola Anna Nery 2020; 24(2) doi: 10.1590/2177-9465-ean-2019-0194
|
31 |
Raghad Al-Abdwani, Ahmed Al Farsi, Matthew Zachariah, Badriya Al Adawi, Azza Al-Rashdi, Naga Ram Dhande, Nagi Elsidig, Zaid Alhinai. Septic shock and fulminant hepatic failure secondary to Q fever in a child with sickle cell disease: First case report. International Journal of Infectious Diseases 2024; 148: 107243 doi: 10.1016/j.ijid.2024.107243
|
32 |
Nicolas S. Merle, Romain Paule, Juliette Leon, Marie Daugan, Tania Robe-Rybkine, Victoria Poillerat, Carine Torset, Véronique Frémeaux-Bacchi, Jordan D. Dimitrov, Lubka T. Roumenina. P-selectin drives complement attack on endothelium during intravascular hemolysis in TLR-4/heme-dependent manner. Proceedings of the National Academy of Sciences 2019; 116(13): 6280 doi: 10.1073/pnas.1814797116
|
33 |
Ashwini Nagaraghatta Shashidhara, Anupama Patil, Chhagan Bihari. Co‐existing nontransfusion‐dependent haemoglobinopathies cause greater clinical and pathological severity of chronic liver disease. GastroHep 2021; 3(2): 100 doi: 10.1002/ygh2.445
|
34 |
Mengna Zhang, William B. Hillegass, Xue Yu, Suvankar Majumdar, J. Daryl Pollard, Erin Jackson, Jarrod Knudson, Douglas Wolfe, Gregory J. Kato, Joseph F. Maher, Hao Mei. Genetic variants and effect modifiers of QT interval prolongation in patients with sickle cell disease. Gene 2024; 890: 147824 doi: 10.1016/j.gene.2023.147824
|
35 |
Shu Kwun Lui, Alyssa Krasinskas, Rushikesh Shah, Jessica M. Tracht. Orthotropic Liver Transplantation for Acute Intrahepatic Cholestasis in Sickle Cell Disease: Clinical and Histopathologic Features of a Rare Case. International Journal of Surgical Pathology 2019; 27(4): 411 doi: 10.1177/1066896918798467
|
36 |
Asa Ramdath, Ahmad Zeineddin, Wasay Nizam, LaDonna Kearse, Olubode A. Olufajo, Mallory Williams. Outcomes after Cholecystectomy in Patients with Sickle Cell Disease: Does Acuity of Presentation Play a Role?. Journal of the American College of Surgeons 2020; 230(6): 1020 doi: 10.1016/j.jamcollsurg.2020.02.046
|
37 |
Shenise N. Gilyard, Scott L. Hamlin, Jamlik-Omari Johnson, Keith D. Herr. Imaging review of sickle cell disease for the emergency radiologist. Emergency Radiology 2021; 28(1): 153 doi: 10.1007/s10140-020-01828-8
|
38 |
Tirthadipa Pradhan-Sundd, Gregory J. Kato, Enrico M. Novelli. Molecular mechanisms of hepatic dysfunction in sickle cell disease: lessons from Townes mouse model. American Journal of Physiology-Cell Physiology 2022; 323(2): C494 doi: 10.1152/ajpcell.00175.2022
|
39 |
M.E. Houwing, P.J. de Pagter, E.J. van Beers, B.J. Biemond, E. Rettenbacher, A.W. Rijneveld, E.M. Schols, J.N.J. Philipsen, R.Y.J. Tamminga, K. Fijn van Draat, E. Nur, M.H. Cnossen. Sickle cell disease: Clinical presentation and management of a global health challenge. Blood Reviews 2019; 37: 100580 doi: 10.1016/j.blre.2019.05.004
|
40 |
Kawthar A. Mohamed, Lauren D. Nephew, Harleen Kaur. Sickle cell hepatopathy: An underrecognized and undertreated cause of chronic liver disease. Clinical Liver Disease 2023; 22(6): 229 doi: 10.1097/CLD.0000000000000092
|
41 |
Claire M. de la Calle, Eric D. Young, Nirmish Singla. Hyperbilirubinemia Following Retroperitoneal Mass Resection in a Patient with Sickle Cell Anemia. Urology 2022; 169: e4 doi: 10.1016/j.urology.2022.08.016
|
42 |
Govind Choudhary, Nida Mirza, Swati Patel. Secondary hemophagocytic lymphohistiocytosis in a child with Sickle Cell Anemia and Hepatitis A and Hepatitis E co-infection: A case report. Pediatric Hematology Oncology Journal 2024; 9(1): 28 doi: 10.1016/j.phoj.2024.01.001
|
43 |
Lydia H. Pecker, Nidhi Patel, Susan Creary, Anil Darbari, Emily Riehm Meier, Deepika S. Darbari, Ross M. Fasano. Diverse manifestations of acute sickle cell hepatopathy in pediatric patients with sickle cell disease: A case series. Pediatric Blood & Cancer 2018; 65(8) doi: 10.1002/pbc.27060
|
44 |
Srinivas Srinidhi Vadlapudi, Anshu Srivastava, Praveer Rai, Rajneesh K. Singh, Moinak Sen Sarma, Ujjal Poddar, Rajanikant R. Yadav. Jaundice in a Child with Sickle Cell Anemia: A Case Based Approach. Indian Journal of Pediatrics 2024; 91(1): 73 doi: 10.1007/s12098-023-04747-x
|
45 |
Pierre O. Ankomah, Ogaga Urhie, Kirtan Patolia, Michael Alebich. A 52-Year-Old Man with Abdominal Pain and Jaundice. NEJM Evidence 2024; 3(12) doi: 10.1056/EVIDmr2400285
|
46 |
Rachel N Fields, Suzanne Minor. Chronic Disease Management in Sickle Cell Trait Patients in the Primary Care Setting: A Case Report. Cureus 2020; doi: 10.7759/cureus.11255
|
47 |
Antonio Morabito, Sylvain Le Jeune. Complications chroniques au cours de la drépanocytose chez l’adulte. La Presse Médicale Formation 2021; 2(4): 380 doi: 10.1016/j.lpmfor.2021.09.019
|
48 |
Neethu Menon, Melissa Frei-Jones. Benign Hematologic Disorders in Children. 2021; : 65 doi: 10.1007/978-3-030-49980-8_5
|
49 |
Dimitrios Schizas, Ioannis Katsaros, Elli Karatza, Stylianos Kykalos, Eleftherios Spartalis, Gerasimos Tsourouflis, Dimitrios Dimitroulis, Nikolaos Nikiteas. Concomitant Laparoscopic Splenectomy and Cholecystectomy: A Systematic Review of the Literature. Journal of Laparoendoscopic & Advanced Surgical Techniques 2020; 30(7): 730 doi: 10.1089/lap.2020.0004
|
50 |
Arshan Khan, Bola Nashed, Mohamed Issa, Muhammad Zatmar Khan. Sickle Cell Intrahepatic Cholestasis: Extremely Rare but Fatal Complication of Sickle Cell Disease. Cureus 2022; doi: 10.7759/cureus.22050
|
51 |
Christophe Duvoux, Lorraine Blaise, Jean-Jacques Matimbo, Francky Mubenga, Norbert Ngongang, Monika Hurtova, Alexis Laurent, Jérémy Augustin, Julien Calderaro, Edouard Reizine, Alain Luciani, Anoosha Habibi, Dora Bachir, Geoffroy Vole, Justine Gellen-Dautremer, Vincent Leroy, Eric Levesque, Pablo Bartolucci. The liver in sickle cell disease. La Presse Médicale 2023; 52(4): 104212 doi: 10.1016/j.lpm.2023.104212
|
52 |
Taiba Jibril Afaa, Kokou Hefoume Amegan-Aho, Matilda Tierenye Dono, Eric Odei, Yaw Asante Awuku, Nikhil Pai. Clinical characteristics of paediatric autoimmune hepatitis at a referral hospital in Sub Saharan Africa. PLOS ONE 2020; 15(12): e0239964 doi: 10.1371/journal.pone.0239964
|
53 |
Ganiwu Abdul, William Osei-Wusu, Gordon Akuffo Asare, Samira Daud, Stephen Opoku, Valentine Christian Kodzo Tsatsu Tamakloe, Joseph Frimpong, Benedict Sackey, Wina Ivy Ofori Boadu, Vivian Paintsil, Max Efui Annani-Akollor, Yaw Amo Wiafe, Enoch Odame Anto, Otchere Addai-Mensah, Nnabuike Chibuoke Ngene. Biomarkers of oxidative stress and its nexus with haemoglobin variants and adverse foeto-maternal outcome among women with preeclampsia in a Ghanaian population: A multi-centre prospective study. PLOS ONE 2023; 18(3): e0283638 doi: 10.1371/journal.pone.0283638
|
54 |
Matthew B Anderson, Ryan Layton, Ryan Woods. Acute-on-Chronic Liver Failure From Acquired Hemochromatosis in a Patient With Sickle Cell Disease. Cureus 2023; doi: 10.7759/cureus.46959
|
55 |
Philipp Kasper, Frank Tacke, Hans-Michael Steffen, Guido Michels. Hepatische Dysfunktion bei Patienten mit kardiogenem Schock. Medizinische Klinik - Intensivmedizin und Notfallmedizin 2019; 114(7): 665 doi: 10.1007/s00063-019-00618-6
|
56 |
Abdourahim Chamouine, Thoueiba Saandi, Mathias Muszlak, Juliette Larmaraud, Laurent Lambrecht, Jean Poisson, Julien Balicchi, Serge Pissard, Narcisse Elenga. High fetal hemoglobin level is associated with increased risk of cerebral vasculopathy in children with sickle cell disease in Mayotte. BMC Pediatrics 2020; 20(1) doi: 10.1186/s12887-020-02187-6
|
57 |
Ariel L. Reinish, Suzie A. Noronha. Anemia in the Young and Old. 2019; : 95 doi: 10.1007/978-3-319-96487-4_6
|
58 |
Sandra Rayego‐Mateos, José Luis Morgado‐Pascual, Cristina García‐Caballero, Iolanda Lazaro, Aleix Sala‐Vila, Lucas Opazo‐Rios, Sebastian Mas‐Fontao, Jesús Egido, Marta Ruiz‐Ortega, Juan Antonio Moreno. Intravascular hemolysis triggers NAFLD characterized by a deregulation of lipid metabolism and lipophagy blockade. The Journal of Pathology 2023; 261(2): 169 doi: 10.1002/path.6161
|
59 |
Sagad O O Mohamed, Omer A O Ibrahim, Dahlia A A Mohammad, Almigdad H M Ali. Correlates of gallbladder stones among patients with sickle cell disease: A meta‐analysis. JGH Open 2021; 5(9): 997 doi: 10.1002/jgh3.12622
|
60 |
Mira E. Nicchitta, Douglas J. Grider, David P. LeBel. A Child With Jaundice. Gastroenterology 2022; 163(3): 591 doi: 10.1053/j.gastro.2022.04.040
|
61 |
Sebastian Vogel, Sayuri Kamimura, Taruna Arora, Meghann L. Smith, Luis E.F. Almeida, Christian A. Combs, Swee Lay Thein, Zenaide M.N. Quezado. NLRP3 inflammasome and bruton tyrosine kinase inhibition interferes with upregulated platelet aggregation and in vitro thrombus formation in sickle cell mice. Biochemical and Biophysical Research Communications 2021; 555: 196 doi: 10.1016/j.bbrc.2021.03.115
|
62 |
Florence Lacaille, Slimane Allali, Mariane de Montalembert. The Liver in Sickle Cell Disease. Journal of Pediatric Gastroenterology and Nutrition 2021; 72(1): 5 doi: 10.1097/MPG.0000000000002886
|
63 |
Divit Shah, Dhruv Talwar, Sunil Kumar, Sourya Acharya, Vidyashree Hulkoti. Fulminant dengue hepatitis in sickle cell disease. Journal of Family Medicine and Primary Care 2022; 11(5): 2241 doi: 10.4103/jfmpc.jfmpc_2058_21
|
64 |
Christopher L. Edwards, Sharena Scott, Michaela Boggan, Jordan Meek, Kiera Alston, Aiden Pearson, Alexandria McDougald, McKenzie Broadnax, Mary Wood, Camela S. Barker, Jessica Miller, Elaine Whitworth, Osaffo James, John J. Sollers III, W. Jeff Bryson, Roland Thorpe, Goldie Byrd, Keith E. Whitfield, Shiv Sudhakar, Debra O. Parker, Jonathan Livingston, Nirmish Shah, Kenyon Railey. Intrahepatic cholestasis in sickle cell disease: A review of diagnostic criteria, treatments, and case reports. Journal of the National Medical Association 2023; 115(1): 26 doi: 10.1016/j.jnma.2022.12.004
|
65 |
Abhishek Gour, Dilpreet Kour, Ramajayan Pandian, Mahir Bhardwaj, Sanghapal D. Sawant, Ajay Kumar, Utpal Nandi. Ellagic Acid Exerts Dual Action to Curb the Pathophysiological Manifestations of Sickle Cell Disease and Attenuate the Hydroxyurea-Induced Myelosuppression in Berkeley Mice. ACS Pharmacology & Translational Science 2023; 6(6): 868 doi: 10.1021/acsptsci.3c00026
|
66 |
Parisa L. Moori, Alexios Dosis, Zoheb Ahmad, Ambareen Kausar, Diana Triantafyllopoulou. Acute Pancreatitis as a Complication of Sickle Cell Anaemia. Reports 2018; 1(3): 19 doi: 10.3390/reports1030019
|
67 |
|
68 |
Motasem Alkhayyat, Mohannad Abou Saleh, Mohammad Zmaili, Vedha Sanghi, Tavankit Singh, Carol Rouphael, C Roberto Simons-Linares, Carlos Romero-Marrero, William D Carey, Christina C Lindenmeyer. Successful liver transplantation for acute sickle cell intrahepatic cholestasis: A case report and review of the literature. World Journal of Hepatology 2020; 12(3): 108-115 doi: 10.4254/wjh.v12.i3.108
|
69 |
Toshimitsu Iwasaki, Satoshi Nara, Yuuki Nishimura, Hiroki Ueda, Yoji Kishi, Minoru Esaki, Kazuaki Shimada, Nobuyoshi Hiraoka. Postoperative acute multiple organ failure after hepatectomy in a Nigerian male with sickle cell trait: a case report. Surgical Case Reports 2021; 7(1) doi: 10.1186/s40792-020-01102-6
|
70 |
Giulia M. Martone, Priyanka M. Nanjireddy, Robin A. Craig, Andrew J. Prout, Meghan A. Higman, Kara M. Kelly, Steven J. Ambrusko. Acute hepatic encephalopathy and multiorgan failure in sickle cell disease and COVID‐19. Pediatric Blood & Cancer 2021; 68(5) doi: 10.1002/pbc.28874
|
71 |
Alison S. Towerman, David B. Wilson, Monica L. Hulbert. Epstein–Barr virus‐induced sickle hepatopathy. Pediatric Blood & Cancer 2021; 68(9) doi: 10.1002/pbc.29196
|
72 |
Syed Ahsan Rizvi, Li Ge, Shuan Li, Akash Pandey. Acute Liver Failure in a Sickle Cell Patient. Journal of Pediatric Gastroenterology and Nutrition 2021; 72(2) doi: 10.1097/MPG.0000000000002827
|
73 |
Ahmad N Kassem, Changsu Park, Aarthi Rajkumar. Acute Liver Failure From Sickle Cell Hepatopathy Treated With Exchange Transfusion. Cureus 2021; doi: 10.7759/cureus.15334
|
74 |
Carlos Delgado-Miguel, Juan I. Camps. Simultaneous Robotic-Assisted Splenectomy and Cholecystectomy in Children: Is It Safe and Effective?. Journal of Laparoendoscopic & Advanced Surgical Techniques 2023; doi: 10.1089/lap.2023.0255
|
75 |
Gil Ben Yakov, Disha Sharma, Hawwa Alao, Pallavi Surana, Devika Kapuria, Ohad Etzion, Matthew M. Hsieh, John F. Tisdale, Courtney D. Fitzhugh, David E. Kleiner, Elliot B. Levy, Richard Chang, Elenita Rivera, Amy Huang, Christopher Koh, Theo Heller. Vibration Controlled Transient Elastography (Fibroscan®) in sickle cell liver disease ‐ could we strike while the liver is hard?. British Journal of Haematology 2019; 187(1): 117 doi: 10.1111/bjh.16047
|
76 |
Luís Rodrigues, Sofia Almeida, Catarina Salgado, Cristina Gonçalves. Pediatric Acute Liver Failure in Sickle Cell Disease. GE - Portuguese Journal of Gastroenterology 2022; 29(3): 192 doi: 10.1159/000515469
|
77 |
Ali Wakil, Gopala Koneru, Nyan L. Latt. Hepatology. 2025; : 371 doi: 10.1016/B978-0-443-26710-9.00013-4
|
78 |
Nidhi Popat, Sunil Kumar, Bhavik S Unadkat. Acute Cholelithiasis With Acute Pancreatic Calcifications: A Unique Presentation of Sickle Cell Crisis. Cureus 2022; doi: 10.7759/cureus.30272
|
79 |
Weiping Cao, Tingmei Chen, Wen Jiang, Yinping Geng, Bing Xie, Qin Wang, Xinzhi Wang. Timely identification and successful treatment of acute fatty liver of pregnancy without obvious clinical symptoms. Medicine 2022; 101(5): e28723 doi: 10.1097/MD.0000000000028723
|
80 |
Sree Karthik Pratapa, Sourya Acharya, Yash Gupte, Samarth Shukla. Acute B Virus Hepatitis with Fulminant Hepatic Failure Precipitating Crisis in Sickle Cell Disease. Journal of Evolution of Medical and Dental Sciences 2020; 9(03): 173 doi: 10.14260/jemds/2020/40
|
81 |
Nikhar P. Kinger, Courtney C. Moreno, Frank H. Miller, Pardeep K. Mittal. Abdominal Manifestations of Sickle Cell Disease. Current Problems in Diagnostic Radiology 2021; 50(2): 241 doi: 10.1067/j.cpradiol.2020.05.012
|
82 |
Nadia Solomon, Nicole Segaran, Mohamed Badawy, Khaled M. Elsayes, John S. Pellerito, Douglas S. Katz, Mariam Moshiri, Margarita V. Revzin. Manifestations of Sickle Cell Disorder at Abdominal and Pelvic Imaging. RadioGraphics 2022; 42(4): 1103 doi: 10.1148/rg.210154
|
83 |
Gustavo de Sousa Arantes Ferreira, Clara Antunes Ferreira, André Luis Conde Watanabe, Natália Carvalho Trevizoli, Maria Clara Borges Murta, Ana Virgínia Ferreira Figueira, Carolina de Fatima Couto. Liver Transplantation After Hematopoietic Stem Cell Transplant for the Treatment of Sickle Cell Disease: A Case Report. Transplantation Proceedings 2022; 54(5): 1394 doi: 10.1016/j.transproceed.2022.03.047
|
84 |
Philipp Kasper, Frank Tacke, Hans-Michael Steffen, Guido Michels. Hepatische Dysfunktion bei Patienten mit kardiogenem Schock. Der Gastroenterologe 2019; 14(6): 475 doi: 10.1007/s11377-019-00401-1
|
85 |
Mehdi Nouraie, Allison E. Ashley-Koch, Melanie E. Garrett, Nithya Sritharan, Yingze Zhang, Jane Little, Victor R. Gordeuk, Mark T. Gladwin, Marilyn J. Telen, Gregory J. Kato, Mary Hamer Hodges. Serum albumin is independently associated with higher mortality in adult sickle cell patients: Results of three independent cohorts. PLOS ONE 2020; 15(8): e0237543 doi: 10.1371/journal.pone.0237543
|
86 |
Firmine Olivia Galiba Atipo Tsiba, Clément Pacha Mikia, Jennifer Armandine Elira Samba, Jade Vanessa Nziengui Mboumba, Félix Malanda, Clausina Mikolele Ahoui, Alexis Elira Dokekias, Duran Canatan. Associated Factors of Cholelithiasis among Younger Children with Sickle Cell Disease at the National Reference Center for Sickle Cell Disease in Brazzaville, Congo. Anemia 2023; 2023: 1 doi: 10.1155/2023/8887981
|
87 |
Insia Rizvi, Divya Solipuram, Navneet Kaur, Aqsa Komel, Saba Batool, Jennifer Wang. The enigma of sickle cell hepatopathy: Pathophysiology, clinical manifestations and therapy. British Journal of Haematology 2024; doi: 10.1111/bjh.19620
|
88 |
John Paul Haydek, Cesar Taborda, Rushikesh Shah, Preeti A Reshamwala, Morgan L McLemore, Fuad El Rassi, Saurabh Chawla. Extreme hyperbilirubinemia: An indicator of morbidity and mortality in sickle cell disease. World Journal of Hepatology 2019; 11(3): 287-293 doi: 10.4254/wjh.v11.i3.287
|
89 |
Mirta T. Ito, Sueli M. da Silva Costa, Letícia C. Baptista, Gabriela Q. Carvalho‐Siqueira, Dulcinéia M. Albuquerque, Vinicius M. Rios, Stephanie Ospina‐Prieto, Roberta C. Saez, Karla P. Vieira, Fernando Cendes, Margareth C. Ozelo, Sara Teresinha O. Saad, Fernando F. Costa, Mônica B. Melo. Angiogenesis‐Related Genes in Endothelial Progenitor Cells May Be Involved in Sickle Cell Stroke. Journal of the American Heart Association 2020; 9(3) doi: 10.1161/JAHA.119.014143
|