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For: Foschi FG, Morelli MC, Savini S, Dall’Aglio AC, Lanzi A, Cescon M, Ercolani G, Cucchetti A, Pinna AD, Stefanini GF. Urea cycle disorders: A case report of a successful treatment with liver transplant and a literature review. World J Gastroenterol 2015; 21(13): 4063-4068 [PMID: 25852294 DOI: 10.3748/wjg.v21.i13.4063]
URL: https://www.wjgnet.com/1007-9327/full/v21/i13/4063.htm
Number Citing Articles
1
Jessica L. Schneller, Ciaran M. Lee, Gang Bao, Charles P. Venditti. Genome editing for inborn errors of metabolism: advancing towards the clinicBMC Medicine 2017; 15(1) doi: 10.1186/s12916-017-0798-4
2
Zandra Overgaard Pedersen, Sonja Holm-Yildiz, Tina Dysgaard. Nutritional Interventions for Patients with Mitochondrial POLG-Related Diseases: A Systematic Review on Efficacy and SafetyInternational Journal of Molecular Sciences 2022; 23(18): 10658 doi: 10.3390/ijms231810658
3
Jędrzej Kukułowicz, Krzysztof Pietrzak-Lichwa, Klaudia Klimończyk, Nathalie Idlin, Marek Bajda, Habibeh Khoshbouei. The SLC6A15–SLC6A20 Neutral Amino Acid Transporter Subfamily: Functions, Diseases, and Their Therapeutic RelevancePharmacological Reviews 2024; 76(1): 142 doi: 10.1124/pharmrev.123.000886
4
Jun Xu, Aimin Zhang, Furong Huang. Biallelic mutations in carbamoyl phosphate synthetase 1 induced hyperammonemia in a neonate: A case reportExperimental and Therapeutic Medicine 2020; 20(1): 623 doi: 10.3892/etm.2020.8717
5
Alireza Shamsaeefar, Saman Nikeghbalian, Seyed Mohsen Dehghani, Kourosh Kazemi, Nasrin Motazedian, Bita Geramizadeh, Seyed Ali Malekhosseini. Curative Treatment of Ornithine Transcarbamylase Deficiency With a Liver Transplant: A Case ReportExperimental and Clinical Transplantation 2019; 17(1): 119 doi: 10.6002/ect.2016.0052
6
Marta García Vega, José D. Andrade, Ana Morais, Esteban Frauca, Gema Muñoz Bartolo, María D. Lledín, Ana Bergua, Loreto Hierro. Urea cycle disorders and indications for liver transplantationFrontiers in Pediatrics 2023; 11 doi: 10.3389/fped.2023.1103757
7
Omid Vakili, Alireza Mafi, Morteza Pourfarzam. Liver Disorders Caused by Inborn Errors of MetabolismEndocrine, Metabolic & Immune Disorders - Drug Targets 2024; 24(2): 194 doi: 10.2174/1871530323666230623120935
8
L.D. Smith, U. Garg. Biomarkers in Inborn Errors of Metabolism2017; : 103 doi: 10.1016/B978-0-12-802896-4.00004-3
9
Matthew Nitzahn, Gabriella Allegri, Suhail Khoja, Brian Truong, Georgios Makris, Johannes Häberle, Gerald S. Lipshutz. Split AAV-Mediated Gene Therapy Restores Ureagenesis in a Murine Model of Carbamoyl Phosphate Synthetase 1 DeficiencyMolecular Therapy 2020; 28(7): 1717 doi: 10.1016/j.ymthe.2020.04.011
10
Berna Seker Yilmaz, Paul Gissen. Genetic Therapy Approaches for Ornithine Transcarbamylase DeficiencyBiomedicines 2023; 11(8): 2227 doi: 10.3390/biomedicines11082227
11
Yuko Sumida, Makoto Tsunoda. Development of a Two-Dimensional Liquid Chromatographic Method for Analysis of Urea Cycle Amino AcidsMolecules 2024; 29(3): 700 doi: 10.3390/molecules29030700
12
Avash Kalra, J. P. Norvell. Cause for Confusion: Noncirrhotic Hyperammonemic EncephalopathyClinical Liver Disease 2020; 15(6): 223 doi: 10.1002/cld.929
13
Xiao-Hui Fu, Yu-Hui Hu, Jian-Xiang Liao, Li Chen, Zhan-Qi Hu, Jia-Lun Wen, Shu-Li Chen. Liver transplantation for late-onset ornithine transcarbamylase deficiency: A case reportWorld Journal of Clinical Cases 2022; 10(18): 6156-6162 doi: 10.12998/wjcc.v10.i18.6156
14
Gargi Bhattacharjee, Indra Mani, Nisarg Gohil, Khushal Khambhati, Darren Braddick, Happy Panchasara, Vijai Singh. Precision Medicine for Investigators, Practitioners and Providers2020; : 59 doi: 10.1016/B978-0-12-819178-1.00007-1
15
Chaya N. Murali, John R. Barber, Robert McCarter, Anqing Zhang, Natalie Gallant, Kara Simpson, Naghmeh Dorrani, Greta N. Wilkening, Ron D. Hays, Uta Lichter-Konecki, Lindsay C. Burrage, Sandesh C.S. Nagamani. Health-related quality of life in a systematically assessed cohort of children and adults with urea cycle disordersMolecular Genetics and Metabolism 2023; 140(3): 107696 doi: 10.1016/j.ymgme.2023.107696
16
Patrick C Lee, Brian Truong, Agustin Vega-Crespo, W Blake Gilmore, Kip Hermann, Stephanie AK Angarita, Jonathan K Tang, Katherine M Chang, Austin E Wininger, Alex K Lam, Benjamen E Schoenberg, Stephen D Cederbaum, April D Pyle, James A Byrne, Gerald S Lipshutz. Restoring Ureagenesis in Hepatocytes by CRISPR/Cas9-mediated Genomic Addition to Arginase-deficient Induced Pluripotent Stem CellsMolecular Therapy - Nucleic Acids 2016; 5: e394 doi: 10.1038/mtna.2016.98
17
Susan E. Waisbren, Arianna K. Stefanatos, Teresa M. Y. Kok, Burcu Ozturk‐Hismi. Neuropsychological attributes of urea cycle disorders: A systematic review of the literatureJournal of Inherited Metabolic Disease 2019; 42(6): 1176 doi: 10.1002/jimd.12146
18
Akshay Kumar, Shailesh Advani, Kichloo Asim, Mohamed A. Mohamed, Farah Wani, Jagmeet Singh, Michael Albosta, Nimisha Shiwalkar, Suresh Keshavamurthy. Hyperammonemia in lung transplant patients and its management: a reviewIndian Journal of Thoracic and Cardiovascular Surgery 2022; 38(S2): 335 doi: 10.1007/s12055-021-01319-6
19
Ernie Zuraida Ali, Yuslina Zakaria, Mohd Amran Mohd Radzi, Lock Hock Ngu, Siti Azma Jusoh. Mutation Study of Malaysian Patients with Ornithine Transcarbamylase Deficiency: Clinical, Molecular, and Bioinformatics Analyses of Two Novel Missense Mutations of the OTC GeneBioMed Research International 2018; 2018: 1 doi: 10.1155/2018/4320831
20
Hussein Algahtani, Seham Alameer, Yousef Marzouk, Bader Shirah. Urea cycle disorder misdiagnosed as multiple sclerosis: a case report and review of the literatureThe Neuroradiology Journal 2018; 31(2): 213 doi: 10.1177/1971400917715880
21
O. V. Bugun, N. N. Martynovich, G. P. Bogonosova, T. A. Astahova, L. V. Rychkova. Inherited metabolic diseases: aminoacidopathies, organic acidemia, defects of mitochondrial β-oxidation. A brief overviewActa Biomedica Scientifica 2021; 6(5): 112 doi: 10.29413/ABS.2021-6.5.11
22
W Craig Kemper, Anthony Sertich, Dimitrios A Vrachatis, Damiano Regazzoli-Lancini, Daniel Messiha, Abdelsalam Bensaaud, Gonçalo Costa. Hepatic encephalopathy due to aorto-right ventricular fistula responsive to percutaneous repair: a case reportEuropean Heart Journal - Case Reports 2023; 7(5) doi: 10.1093/ehjcr/ytad169