A case of a Japanese patient with neonatal diabetes mellitus caused by a novel mutation in the ABCC8 gene and successfully controlled with oral glibenclamide.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Works matching IS 09185739 AND DT 2015 AND VI 24 AND IP 4
Results: 6
1
2
An adolescent case of familial hyperparathyroidism with a germline frameshift mutation of the CDC73 gene.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
3
Age at menarche and near final height after treatment with gonadotropin-releasing hormone agonist alone or combined with growth hormone in Korean girls with central precocious puberty.
- Published in:
- Clinical Pediatric Endocrinology, 2015, v. 24, n. 4, p. 175, doi. 10.1297/cpe.24.175
- By:
- Publication type:
- Article
4
Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan.
- Published in:
- Clinical Pediatric Endocrinology, 2015, v. 24, n. 4, p. 167, doi. 10.1297/cpe.24.167
- By:
- Publication type:
- Article
5
The factors affecting on estimation of carbohydrate content of meals in carbohydrate counting.
- Published in:
- Clinical Pediatric Endocrinology, 2015, v. 24, n. 4, p. 153, doi. 10.1297/cpe.24.153
- By:
- Publication type:
- Article
6
Bone age: assessment methods and clinical applications.
- Published in:
- Clinical Pediatric Endocrinology, 2015, v. 24, n. 4, p. 143, doi. 10.1297/cpe.24.143
- By:
- Publication type:
- Article