A case of transient neonatal diabetes due to a novel mutation in ABCC8.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
Works matching IS 09185739 AND DT 2016 AND VI 25 AND IP 4
Results: 4
1
2
A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
3
A patient with pseudohypoaldosteronism type II complicated by congenital hypopituitarism carrying a KLHL3 mutation.
- Published in:
- Clinical Pediatric Endocrinology, 2016, v. 25, n. 4, p. 127, doi. 10.1297/cpe.25.127
- By:
- Publication type:
- Article
4
Longitudinal observation of serum anti-Müllerian hormone in three girls after cancer treatment.
- Published in:
- Clinical Pediatric Endocrinology, 2016, v. 25, n. 4, p. 119, doi. 10.1297/cpe.25.119
- By:
- Publication type:
- Article