| For: | Guo J, Ren D, Guo ZJ, Yu J, Liu F, Zhao RX, Wang Y. Emergence of lesions outside of the basal ganglia and irreversible damage to the basal ganglia with severe β-ketothiolase deficiency: A case report . World J Clin Cases 2021; 9(30): 9276-9284 [PMID: 34786414 DOI: 10.12998/wjcc.v9.i30.9276] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v9/i30/9276.htm |
| Number | Citing Articles |
| 1 |
Berihu Gebre, Yirgalem Gereziher, Dejen Gebrewahd, Catherine Alcober. Beta-ketothiolase deficiency with progressive basal ganglia and extra basal ganglia involvement: CT–MRI correlation in a pediatric metabolic encephalopathy: A case report. Radiology Case Reports 2026; 21(10) doi: 10.1016/j.radcr.2026.06.125
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| 3 |
Sohit Kashyap, Anil Kumar, Anita Choudhary, Ajay Kumar, Arvinder Wander, Anjana Munshi. Beta-Ketothiolase Deficiency: A Comprehensive Review of Genetic Variants and Pathophysiology. Annals of Child Neurology 2025; 33(4) doi: 10.26815/acn.2025.00941
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| 4 |
Nurcan Üçüncü Ergun, Nihal Coşkun, Merve Aslantaş, Meyrem Aybike Kurtbeyoğlu Köse. Longitudinal biochemical profiles in beta-ketothiolase deficiency: Phase-dependent diagnostic challenges and metabolic variability. Molecular Genetics and Metabolism 2026; 149(1-2) doi: 10.1016/j.ymgme.2026.110244
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| 5 |
Xi Deng, Xinting Li, Haoran Liu, Tao Wang, Fang Tang, Qingti Tan, Yu Feng, Xiaoli Luo. Beta-ketothiolase deficiency: two novel ACAT1 variants and a retrospective study of 76 cases in China. Molecular Genetics and Metabolism 2026; 149(1-2) doi: 10.1016/j.ymgme.2026.110242
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