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Natural history and outcome of nonketotic hyperglycinemia in China.
- Published in:
- Frontiers in Neurology, 2024, p. 01, doi. 10.3389/fneur.2024.1440883
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- Publication type:
- Article
Features of liver injury in 138 Chinese patients with NICCD.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2023, v. 36, n. 12, p. 1154, doi. 10.1515/jpem-2023-0026
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- Publication type:
- Article
First case report of medium-chain acyl-coenzyme A dehydrogenase deficiency in China.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 5/6, p. 681, doi. 10.1515/jpem-2014-0058
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- Publication type:
- Article
First case report of short-chain acyl-CoA dehydrogenase deficiency in China.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2012, v. 25, n. 7/8, p. 795, doi. 10.1515/jpem-2012-0185
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- Publication type:
- Article
First case report of short-chain acyl-CoA dehydrogenase deficiency in China.
- Published in:
- 2013
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- Publication type:
- Abstract
Clinical and genetic analysis of methylmalonic aciduria in 60 patients from Southern China: a single center retrospective study.
- Published in:
- Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03210-0
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- Publication type:
- Article
Human iPSC-derived neural stem cells with ALDH5A1 mutation as a model of succinic semialdehyde dehydrogenase deficiency.
- Published in:
- BMC Neuroscience, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s12868-022-00755-3
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- Publication type:
- Article