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For: Matsumoto S, Häberle J, Kido J, Mitsubuchi H, Endo F, Nakamura K. Urea cycle disorders-update. J Hum Genet 2019;64:833-47. [PMID: 31110235 DOI: 10.1038/s10038-019-0614-4] [Cited by in Crossref: 31] [Cited by in F6Publishing: 25] [Article Influence: 10.3] [Reference Citation Analysis]
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9 Enosawa S, Hsu HC, Yanagi Y, Matsunari H, Uchikura A, Nagashima H. Characterization and Treatment Responsiveness of Genetically Engineered Ornithine Transcarbamylase-Deficient Pig. J Clin Med 2021;10:3226. [PMID: 34362010 DOI: 10.3390/jcm10153226] [Reference Citation Analysis]
10 Liu F, Bao LS, Liang RJ, Zhao XY, Li Z, Du ZF, Lv SG. Identification of rare variants causing urea cycle disorders: A clinical, genetic, and biophysical study. J Cell Mol Med 2021;25:4099-109. [PMID: 33611823 DOI: 10.1111/jcmm.16379] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
11 Zhou Q, Huang H, Ma L, Zhu T. The Application of Next-Generation Sequencing (NGS) in Neonatal-Onset Urea Cycle Disorders (UCDs): Clinical Course, Metabolomic Profiling, and Genetic Findings in Nine Chinese Hyperammonemia Patients. Biomed Res Int 2020;2020:5690915. [PMID: 32934962 DOI: 10.1155/2020/5690915] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
12 Zabaleta N, Hommel M, Salas D, Gonzalez-aseguinolaza G. Genetic-Based Approaches to Inherited Metabolic Liver Diseases. Human Gene Therapy 2019;30:1190-203. [DOI: 10.1089/hum.2019.140] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 3.7] [Reference Citation Analysis]
13 Ravindranath A, Sarma MS. Mitochondrial hepatopathy: Anticipated difficulties in management of fatty acid oxidation defects and urea cycle defects. World J Hepatol 2022; 14(1): 180-194 [DOI: 10.4254/wjh.v14.i1.180] [Reference Citation Analysis]
14 Amodio P, Montagnese S. Lights and Shadows in Hepatic Encephalopathy Diagnosis. J Clin Med 2021;10:341. [PMID: 33477554 DOI: 10.3390/jcm10020341] [Reference Citation Analysis]
15 Imagawa E, Diaz GA, Oishi K. A novel Romani microdeletion variant in the promoter sequence of ASS1 causes citrullinemia type I. Mol Genet Metab Rep 2020;24:100619. [PMID: 32637322 DOI: 10.1016/j.ymgmr.2020.100619] [Reference Citation Analysis]
16 Žigman T, Petković Ramadža D, Šimić G, Barić I. Inborn Errors of Metabolism Associated With Autism Spectrum Disorders: Approaches to Intervention. Front Neurosci 2021;15:673600. [PMID: 34121999 DOI: 10.3389/fnins.2021.673600] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
17 Leger RF, Silverman MS, Hauck ES, Guvakova KD. Hyperammonemia Post Lung Transplantation: A Review. Clin Med Insights Circ Respir Pulm Med 2020;14:1179548420966234. [PMID: 33192115 DOI: 10.1177/1179548420966234] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
18 Zhang M, Wang S, Sun L, Gan L, Lin Y, Shao J, Jiang H, Li M. Ammonia induces changes in carbamoyl phosphate synthetase I and its regulation of glutamine synthesis and urea cycle in yellow catfish Pelteobagrus fulvidraco. Fish Shellfish Immunol 2021;120:242-51. [PMID: 34856372 DOI: 10.1016/j.fsi.2021.11.023] [Reference Citation Analysis]
19 Muthaffar OY. Treating epilepsy with options other than antiepileptic medications. Neurosciences (Riyadh) 2020;25:253-61. [PMID: 33130805 DOI: 10.17712/nsj.2020.4.20200010] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
20 Vernon HJ, Manoli I. Milestones in treatments for inborn errors of metabolism: Reflections on Where chemistry and medicine meet. Am J Med Genet A 2021. [PMID: 34165242 DOI: 10.1002/ajmg.a.62385] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Geller S, Lieberman H, Belanger AJ, Yew NS, Kloss A, Ivanov AR. Comparison of Microflow and Analytical Flow Liquid Chromatography Coupled to Mass Spectrometry Global Metabolomics Methods Using a Urea Cycle Disorder Mouse Model. J Proteome Res 2021. [PMID: 34843255 DOI: 10.1021/acs.jproteome.1c00628] [Reference Citation Analysis]
22 Lee JJ, Cho S, Kim BK, Kwon O, Park JM, Lee WW, Kang K. Recurrent Altered Mental State Associated with Nonhepatic Hyperammonemia Presented in an Elderly Female Patient: Probable Late-Onset Urea Cycle Disorder. J Epilepsy Res 2021;11:96-9. [PMID: 34395229 DOI: 10.14581/jer.21013] [Reference Citation Analysis]
23 Li J, Li R, Gao Y, Jin X, Zhang J, Ren J, Hou Y, Wang X, Wang G. Increasing serum ammonia level is a risk factor for the prognosis of critically ill patients: A multicenter retrospective cohort study. J Crit Care 2021;62:218-22. [PMID: 33429115 DOI: 10.1016/j.jcrc.2020.12.028] [Reference Citation Analysis]
24 Li M, Zhang M, Qian Y, Shi G, Wang R. Ammonia toxicity in the yellow catfish (Pelteobagrus fulvidraco): The mechanistic insight from physiological detoxification to poisoning. Fish & Shellfish Immunology 2020;102:195-202. [DOI: 10.1016/j.fsi.2020.04.042] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 7.0] [Reference Citation Analysis]
25 Song P, Li M, Zhang M, Jiang H, Shao J, Wang R, Qian Y, Feng D. Inhibition of argininosuccinate synthase (ASS) affected ammonia excretion in yellow catfish Pelteobagrus fulvidraco during acute ammonia poisoning. Aquaculture Reports 2022;22:100931. [DOI: 10.1016/j.aqrep.2021.100931] [Reference Citation Analysis]
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27 Magalhães T, Campos T, Rodrigues E, Vasconcelos C, Fontoura M, Vilarinho L, Leão-Teles E. Hyperammonaemic encephalopathy in a teenage girl. J Paediatr Child Health 2021. [PMID: 34725893 DOI: 10.1111/jpc.15824] [Reference Citation Analysis]
28 Vimalesvaran S, Dhawan A. Liver transplantation for pediatric inherited metabolic liver diseases. World J Hepatol 2021; 13(10): 1351-1366 [PMID: 34786171 DOI: 10.4254/wjh.v13.i10.1351] [Reference Citation Analysis]
29 Saito Y, Ikemoto T, Tokuda K, Miyazaki K, Yamada S, Imura S, Miyake M, Morine Y, Oyadomari S, Shimada M. Effective three-dimensional culture of hepatocyte-like cells generated from human adipose-derived mesenchymal stem cells. J Hepatobiliary Pancreat Sci 2021. [PMID: 34318615 DOI: 10.1002/jhbp.1024] [Reference Citation Analysis]
30 Ingoglia F, Chong JL, Pasquali M, Longo N. Creatine metabolism in patients with urea cycle disorders. Mol Genet Metab Rep 2021;29:100791. [PMID: 34471603 DOI: 10.1016/j.ymgmr.2021.100791] [Reference Citation Analysis]
31 Tinkov AA, Skalnaya MG, Skalny AV. Serum trace element and amino acid profile in children with cerebral palsy. J Trace Elem Med Biol 2021;64:126685. [PMID: 33249374 DOI: 10.1016/j.jtemb.2020.126685] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
32 Wang L, Zheng R, Xu Y, Zhou Z, Guan P, Wu Y, Zhou J, Cheng Z, Zhang L. Altered Metabolic Characteristics in Plasma of Young Boys with Autism Spectrum Disorder. J Autism Dev Disord 2021. [PMID: 34800227 DOI: 10.1007/s10803-021-05364-3] [Reference Citation Analysis]
33 Zheng Z, Lin Y, Lin W, Zhu L, Jiang M, Wang W, Fu Q. Clinical and genetic analysis of five Chinese patients with urea cycle disorders. Mol Genet Genomic Med 2020;8:e1301. [PMID: 32410394 DOI: 10.1002/mgg3.1301] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
34 Zabulica M, Jakobsson T, Ravaioli F, Vosough M, Gramignoli R, Ellis E, Rooyackers O, Strom SC. Gene Editing Correction of a Urea Cycle Defect in Organoid Stem Cell Derived Hepatocyte-like Cells. Int J Mol Sci 2021;22:1217. [PMID: 33530582 DOI: 10.3390/ijms22031217] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
35 Sen K, Whitehead M, Castillo Pinto C, Caldovic L, Gropman A. Fifteen years of urea cycle disorders brain research: Looking back, looking forward. Anal Biochem 2021;:114343. [PMID: 34637785 DOI: 10.1016/j.ab.2021.114343] [Reference Citation Analysis]