Works matching IS 09185739 AND DT 2013 AND VI 22 AND IP 4
Results: 5
A Novel Deletion Mutation of SLC16A2 Encoding Monocarboxylate Transporter (MCT) 8 in a 26-year-old Japanese Patient with Allan-Herndon-Dudley Syndrome.
- Published in:
- Clinical Pediatric Endocrinology, 2013, v. 22, n. 4, p. 83, doi. 10.1297/cpe.22.83
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- Publication type:
- Article
Brain White Matter Abnormality in a Newborn Infant with Congenital Adrenal Hyperplasia.
- Published in:
- Clinical Pediatric Endocrinology, 2013, v. 22, n. 4, p. 77, doi. 10.1297/cpe.22.77
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- Publication type:
- Article
A Case of Vitamin D Deficiency without Elevation of Serum Alkaline Phosphatase in a Carrier of Hypophosphatasia.
- Published in:
- Clinical Pediatric Endocrinology, 2013, v. 22, n. 4, p. 73, doi. 10.1297/cpe.22.73
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- Publication type:
- Article
Therapeutic Efficacy and Safety of GH in Japanese Children with Down Syndrome Short Stature Accompanied by GH Deficiency.
- Published in:
- Clinical Pediatric Endocrinology, 2013, v. 22, n. 4, p. 65, doi. 10.1297/cpe.22.65
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- Publication type:
- Article
Abnormal Adipose Tissue Distribution with Unfavorable Metabolic Profile in Five Children Following Hematopoietic Stem Cell Transplantation: A New Etiology for Acquired Partial Lipodystrophy.
- Published in:
- Clinical Pediatric Endocrinology, 2013, v. 22, n. 4, p. 53, doi. 10.1297/cpe.22.53
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- Publication type:
- Article