Corrigenda.
- Published in:
- Clinical Pediatric Endocrinology, 2019, v. 28, n. 1, p. 23, doi. 10.1297/cpe.28.23
- Publication type:
- Article
Works matching IS 09185739 AND DT 2019 AND VI 28 AND IP 1
Results: 5
1
2
Mutation-in-Brief: A Japanese case of familial hypercholesterolemia with a novel mutation in the LDLR gene.
- Published in:
- Clinical Pediatric Endocrinology, 2019, v. 28, n. 1, p. 19, doi. 10.1297/cpe.28.19
- By:
- Publication type:
- Article
3
A case of pseudohypoparathyroidism type la with a novel frameshift mutation in the GNAS gene: early diagnosis of osteoma cutis by skin biopsy.
- Published in:
- Clinical Pediatric Endocrinology, 2019, v. 28, n. 1, p. 15, doi. 10.1297/cpe.28.15
- By:
- Publication type:
- Article
4
Combination therapy of propranolol, levothyroxine, and liothyronine was effective in a case of severe consumptive hypothyroidism associated with infantile hepatic hemangioma.
- Published in:
- Clinical Pediatric Endocrinology, 2019, v. 28, n. 1, p. 9, doi. 10.1297/cpe.28.9
- By:
- Publication type:
- Article
5
Case Report Metreleptin treatment for congenital generalized lipodystrophy type 4 (CGL4): a case report.
- Published in:
- Clinical Pediatric Endocrinology, 2019, v. 28, n. 1, p. 1, doi. 10.1297/cpe.28.1
- By:
- Publication type:
- Article