Responses to the Letter to the Editor "Does growth-hormone treatment affect patients with and without a mitochondrial disorder differentially ?" (Vol. 27, No. 2, p. 107-108, 2018).
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Works matching IS 09185739 AND DT 2018 AND VI 27 AND IP 3
Results: 14
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A pediatric case of insulinoma and a novel MEN1 mutation: the efficacy of the combination therapy of diazoxide and cornstarch.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 3, p. 197, doi. 10.1297/cpe.27.197
- By:
- Publication type:
- Article
3
A familial case of spondyloepiphyseal dysplasia tarda caused by a novel splice site mutation in TRAPPC2.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 3, p. 193, doi. 10.1297/cpe.27.193
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- Publication type:
- Article
4
Vitamin D deficiency associated with dilated cardiomyopathy in early infancy caused by maternal cholestasis.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 3, p. 187, doi. 10.1297/cpe.27.187
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- Publication type:
- Article
5
A case of perinatal hypophosphatasia with a novel mutation in the ALPL gene: clinical course and review of the literature.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 3, p. 179, doi. 10.1297/cpe.27.179
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- Publication type:
- Article
6
Therapy with propylthiouracil for T3-predominant neonatal Graves' disease: a case report.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 3, p. 171, doi. 10.1297/cpe.27.171
- By:
- Publication type:
- Article
7
Sexual precocity in a girl with early-onset Graves' disease.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 3, p. 165, doi. 10.1297/cpe.27.165
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- Publication type:
- Article
8
Novel heterozygous mutation in TBX1 in an infant with hypocalcemic seizures.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
9
Long-term safety and efficacy of daily recombinant human growth hormone treatment in Japanese short children born small for gestational age: final report from an open and multi-center study.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 3, p. 145, doi. 10.1297/cpe.27.145
- By:
- Publication type:
- Article
10
Safety and effectiveness, including intelligence prognosis, of diazoxide in pediatric patients with hyperinsulinemic hypoglycemia: special survey in Japan (long-term, all-case survey).
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 3, p. 131, doi. 10.1297/cpe.27.131
- By:
- Publication type:
- Article
11
Identification of compound heterozygous TSHR mutations (R109Q and R450H) in a patient with nonclassic TSH resistance and functional characterization of the mutant receptors.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 3, p. 123, doi. 10.1297/cpe.27.123
- By:
- Publication type:
- Article
12
Uniparental disomy as a cause of pediatric endocrine disorders.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 3, p. 113, doi. 10.1297/cpe.27.113
- By:
- Publication type:
- Article
13
Three practical principles in planning and developing health care transition: our personal perspectives.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 3, p. 109, doi. 10.1297/cpe.27.109
- By:
- Publication type:
- Article
14
Memoriam: Teruo Kitagawa, MD, PhD (1926-2017).
- Published in:
- 2018
- By:
- Publication type:
- Obituary