Works matching IS 09185739 AND DT 2017 AND VI 26 AND IP 4
Results: 8
A Japanese boy with fructose-1,6-bisphosphatase deficiency who had a novel FBP1 mutation (p.Phe90Val).
- Published in:
- Clinical Pediatric Endocrinology, 2017, v. 26, n. 4, p. 275, doi. 10.1297/cpe.26.275
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- Article
Five cases of childhood-onset Graves' disease treated with either surgery or radio-iodine therapy.
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- Clinical Pediatric Endocrinology, 2017, v. 26, n. 4, p. 265, doi. 10.1297/cpe.26.265
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- Article
A case of an infant with congenital combined pituitary hormone deficiency and normalized liver histology of infantile cholestasis after hormone replacement therapy.
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- Clinical Pediatric Endocrinology, 2017, v. 26, n. 4, p. 251, doi. 10.1297/cpe.26.251
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- Article
Detection of early stage medullary thyroid carcinoma by measuring serum calcitonin using an electro chemiluminescence immuno-assay: A case report of a young Japanese woman with a high-risk RET mutation.
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- Clinical Pediatric Endocrinology, 2017, v. 26, n. 4, p. 243, doi. 10.1297/cpe.26.243
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- Article
Incidence of diabetes mellitus and neoplasia in Japanese short-statured children treated with growth hormone in the Genetics and Neuroendocrinology of Short Stature International Study (GeNeSIS).
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- Clinical Pediatric Endocrinology, 2017, v. 26, n. 4, p. 229, doi. 10.1297/cpe.26.229
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- Article
Longitudinal study on the effectiveness of vitamin D supplements in exclusively breast-fed infants.
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- Clinical Pediatric Endocrinology, 2017, v. 26, n. 4, p. 215, doi. 10.1297/cpe.26.215
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- Article
Clinical characteristics of septo-optic dysplasia accompanied by congenital central hypothyroidism in Japan.
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- Clinical Pediatric Endocrinology, 2017, v. 26, n. 4, p. 207, doi. 10.1297/cpe.26.207
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- Publication type:
- Article
Characteristic clinical features of adipsic hypernatremia patients with subfornical organ-targeting antibody.
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- Clinical Pediatric Endocrinology, 2017, v. 26, n. 4, p. 197, doi. 10.1297/cpe.26.197
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- Article