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 clinic. BMC 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 Safety. International 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 Relevance. Pharmacological 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 report. Experimental and Therapeutic Medicine 2020; 20(1): 623 doi: 10.3892/etm.2020.8717
|
5 |
Samantha A. Schrier Vergano. Intellectual and Developmental Disabilities. Contemporary Clinical Neuroscience 2024; : 119 doi: 10.1007/978-3-031-66932-3_7
|
6 |
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 Report. Experimental and Clinical Transplantation 2019; 17(1): 119 doi: 10.6002/ect.2016.0052
|
7 |
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 transplantation. Frontiers in Pediatrics 2023; 11 doi: 10.3389/fped.2023.1103757
|
8 |
Omid Vakili, Alireza Mafi, Morteza Pourfarzam. Liver Disorders Caused by Inborn Errors of Metabolism. Endocrine, Metabolic & Immune Disorders - Drug Targets 2024; 24(2): 194 doi: 10.2174/1871530323666230623120935
|
9 |
L.D. Smith, U. Garg. Biomarkers in Inborn Errors of Metabolism. 2017; : 103 doi: 10.1016/B978-0-12-802896-4.00004-3
|
10 |
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 Deficiency. Molecular Therapy 2020; 28(7): 1717 doi: 10.1016/j.ymthe.2020.04.011
|
11 |
Berna Seker Yilmaz, Paul Gissen. Genetic Therapy Approaches for Ornithine Transcarbamylase Deficiency. Biomedicines 2023; 11(8): 2227 doi: 10.3390/biomedicines11082227
|
12 |
Yuko Sumida, Makoto Tsunoda. Development of a Two-Dimensional Liquid Chromatographic Method for Analysis of Urea Cycle Amino Acids. Molecules 2024; 29(3): 700 doi: 10.3390/molecules29030700
|
13 |
Avash Kalra, J. P. Norvell. Cause for Confusion: Noncirrhotic Hyperammonemic Encephalopathy. Clinical Liver Disease 2020; 15(6): 223 doi: 10.1002/cld.929
|
14 |
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 report. World Journal of Clinical Cases 2022; 10(18): 6156-6162 doi: 10.12998/wjcc.v10.i18.6156
|
15 |
Gargi Bhattacharjee, Indra Mani, Nisarg Gohil, Khushal Khambhati, Darren Braddick, Happy Panchasara, Vijai Singh. Precision Medicine for Investigators, Practitioners and Providers. 2020; : 59 doi: 10.1016/B978-0-12-819178-1.00007-1
|
16 |
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 disorders. Molecular Genetics and Metabolism 2023; 140(3): 107696 doi: 10.1016/j.ymgme.2023.107696
|
17 |
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 Cells. Molecular Therapy - Nucleic Acids 2016; 5: e394 doi: 10.1038/mtna.2016.98
|
18 |
Susan E. Waisbren, Arianna K. Stefanatos, Teresa M. Y. Kok, Burcu Ozturk‐Hismi. Neuropsychological attributes of urea cycle disorders: A systematic review of the literature. Journal of Inherited Metabolic Disease 2019; 42(6): 1176 doi: 10.1002/jimd.12146
|
19 |
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 review. Indian Journal of Thoracic and Cardiovascular Surgery 2022; 38(S2): 335 doi: 10.1007/s12055-021-01319-6
|
20 |
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 Gene. BioMed Research International 2018; 2018: 1 doi: 10.1155/2018/4320831
|
21 |
Hussein Algahtani, Seham Alameer, Yousef Marzouk, Bader Shirah. Urea cycle disorder misdiagnosed as multiple sclerosis: a case report and review of the literature. The Neuroradiology Journal 2018; 31(2): 213 doi: 10.1177/1971400917715880
|
22 |
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 overview. Acta Biomedica Scientifica 2021; 6(5): 112 doi: 10.29413/ABS.2021-6.5.11
|
23 |
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 report. European Heart Journal - Case Reports 2023; 7(5) doi: 10.1093/ehjcr/ytad169
|
24 |
Dunia Abbas Khudhair, Hadeel Luay Kareem, Mohmmed Ali Yaseen, Hussam A. Mohammed. Assessment of Arginase II with Biochemical Changes in Patients with Chronic Kidney Disease. Medical Journal of Babylon 2024; 21(3): 748 doi: 10.4103/MJBL.MJBL_1682_23
|