Found: 8
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Dp71 and intellectual disability in Indonesian patients with Duchenne muscular dystrophy.
- Published in:
- PLoS ONE, 2022, v. 17, n. 10, p. 1, doi. 10.1371/journal.pone.0276640
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- Publication type:
- Article
The PPARGC1A Is the Gene Responsible for Thrifty Metabolism Related Metabolic Diseases: A Scoping Review.
- Published in:
- Genes, 2022, v. 13, n. 10, p. N.PAG, doi. 10.3390/genes13101894
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- Publication type:
- Article
Linear growth and systemic glucocorticoid therapy in children with systemic lupus erythematosus.
- Published in:
- Paediatrica Indonesiana, 2022, v. 62, n. 1, p. 37, doi. 10.14238/pi62.1.2022.37-43
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- Publication type:
- Article
Predictive factors of ketoacidosis in type 1 diabetes mellitus.
- Published in:
- Paediatrica Indonesiana, 2019, v. 59, n. 4, p. 169, doi. 10.14238/pi59.4.2019.169-74
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- Publication type:
- Article
Effect of <italic>FTO</italic> rs9939609 variant on insulin resistance in obese female adolescents.
- Published in:
- BMC Research Notes, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13104-018-3392-8
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- Publication type:
- Article
Phaeochromocytoma in a teenage girl with Cushing's Syndrome.
- Published in:
- 2013
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- Publication type:
- Abstract
Novel SCN1A mutations in Indonesian patients with severe myoclonic epilepsy in infancy.
- Published in:
- Pediatrics International, 2010, v. 52, n. 2, p. 234, doi. 10.1111/j.1442-200X.2009.02916.x
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- Publication type:
- Article
Early cardiac failure in a child with Becker muscular dystrophy is due to an abnormally low amount of dystrophin transcript lacking exon 13.
- Published in:
- Pediatrics International, 1997, v. 39, n. 6, p. 685, doi. 10.1111/j.1442-200X.1997.tb03668.x
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- Publication type:
- Article