Works matching IS 09185739 AND DT 2015 AND VI 24 AND IP 3
Results: 5
Two Japanese patients with the renal form of pseudohypoaldosteronism type 1 caused by mutations of NR3C2.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision).
- Published in:
- Clinical Pediatric Endocrinology, 2015, v. 24, n. 3, p. 107
- By:
- Publication type:
- Article
Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision).
- Published in:
- Clinical Pediatric Endocrinology, 2015, v. 24, n. 3, p. 77
- By:
- Publication type:
- Article
Single serum cortisol values at 09:00 h can be indices of adrenocortical function in children with Kawasaki disease treated with intravenous immunoglobulin plus prednisolone.
- Published in:
- Clinical Pediatric Endocrinology, 2015, v. 24, n. 3, p. 69, doi. 10.1297/cpe.24.69
- By:
- Publication type:
- Article
A case of spondyloepiphyseal dysplasia tarda caused by a novel intragenic deletion of TRAPPC2.
- Published in:
- 2015
- By:
- Publication type:
- Case Study