For: | Wang XC, Wang T, Liu RH, Jiang Y, Chen DD, Wang XY, Kong QX. Child with adenylosuccinate lyase deficiency caused by a novel complex heterozygous mutation in the ADSL gene: A case report. World J Clin Cases 2022; 10(30): 11082-11089 [PMID: 36338215 DOI: 10.12998/wjcc.v10.i30.11082] |
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URL: | https://www.wjgnet.com/2307-8960/full/v10/i30/11082.htm |
Number | Citing Articles |
1 |
Athanasia Sesse, Paris Ladias, Charilaos Kostoulas, Dimitrios Chatzistefanidis, Ioannis Georgiou, Sofia Markoula. Metabolic pathways and genes involved in treatable and non-treatable metabolic epilepsies. A comprehensive review and metabolic pathway analysis. Metabolic Brain Disease 2025; 40(3) doi: 10.1007/s11011-025-01562-5
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2 |
Albert Frank Magnusen, Robert James Hopkin, Charles Vorhees, Elizabeth Wilson, Molly Moehlman, Barbara Hallinan, Craig Erickson, Melissa P. DelBello, Luca Marsili, Nicole G. Coufal, Manoj Kumar Pandey. Emerging role of complement system in the induction of neuroinflammation in adenylosuccinate lyase deficiency disorder. Brain, Behavior, & Immunity - Health 2025; 48: 101091 doi: 10.1016/j.bbih.2025.101091
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3 |
Marcella Camici, Mercedes Garcia-Gil, Simone Allegrini, Rossana Pesi, Giulia Bernardini, Vanna Micheli, Maria Grazia Tozzi. Inborn Errors of Purine Salvage and Catabolism. Metabolites 2023; 13(7): 787 doi: 10.3390/metabo13070787
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