Works matching IS 09185739 AND DT 2018 AND VI 27
Results: 38
Methylome analysis of thyroid ectopy shows no disease-specific DNA methylation signature.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 4, p. 235, doi. 10.1297/cpe.27.235
- By:
- Publication type:
- Article
Efficacy and safety of growth hormone treatment in Japanese children with small-for-gestational-age short stature in accordance with Japanese guidelines.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 4, p. 225, doi. 10.1297/cpe.27.225
- By:
- Publication type:
- Article
Establishment of a longitudinal growth chart corresponding to pubertal timing.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 4, p. 215, doi. 10.1297/cpe.27.215
- By:
- Publication type:
- Article
Health problems of adolescent and adult patients with 21-hydroxylase deficiency.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 4, p. 203, doi. 10.1297/cpe.27.203
- By:
- Publication type:
- Article
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
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
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
- By:
- Publication type:
- Article
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
- By:
- Publication type:
- Article
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
- By:
- Publication type:
- Article
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
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
- By:
- Publication type:
- Article
Novel heterozygous mutation in TBX1 in an infant with hypocalcemic seizures.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
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
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
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
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
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
Memoriam: Teruo Kitagawa, MD, PhD (1926-2017).
- Published in:
- 2018
- By:
- Publication type:
- Obituary
A pediatric case of pheochromocytoma without apparent hypertension associated with von Hippel-Lindau disease.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Thyroid nodules and long-term follow-up among childhood cancer survivors who underwent hematopoietic stem cell transplantation.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Two siblings with congenital central hypothyroidism caused by a novel mutation in the IGSF1 gene.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Decrement in bone mineral density after parathyroidectomy in a pediatric patient with primary hyperparathyroidism.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Does growth-hormone treatment affect patients with and without a mitochondrial disorder differentially?
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Chromosome 6q24-related diabetes mellitus.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 2, p. 59, doi. 10.1297/cpe.27.59
- By:
- Publication type:
- Article
Recombinant human growth hormone in neonatalonset multisystem inflammatory disease.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Thyroid hormone status in patients with severe selenium deficiency.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 2, p. 67, doi. 10.1297/cpe.27.67
- By:
- Publication type:
- Article
広報委員会办右願1、匕朽知6甘.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, p. 11
- Publication type:
- Article
卒後教育入門7専門七芝于一刃二案内.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, p. 10
- Publication type:
- Article
2016年度第6回理事会議事録.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, p. 5
- Publication type:
- Article
I.第52回日本小児内分泌学会学術集会0 二案内.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, p. 3
- Publication type:
- Article
A follow-up during puberty in a Japanese girl with type A insulin resistance due to a novel mutation in INSR.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 1, p. 53, doi. 10.1297/cpe.27.53
- By:
- Publication type:
- Article
Chiari type 1 malformation associated with central sleep apnea after high dose growth hormone (GH) therapy in a 12-year-old boy: A case report.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 1, p. 45, doi. 10.1297/cpe.27.45
- By:
- Publication type:
- Article
Fluctuation of blood glucose levels in an infant with an ileostomy on continuous glucose monitoring: A case report.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 1, p. 39, doi. 10.1297/cpe.27.39
- By:
- Publication type:
- Article
Perinatal factors affecting growth and development at age 3 years in extremely low birth weight infants born small for gestational age.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 1, p. 31, doi. 10.1297/cpe.27.31
- By:
- Publication type:
- Article
Postnatal BMI changes in children with different birthweights: A trial study for detecting early predictive factors for pediatric obesity.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 1, p. 19, doi. 10.1297/cpe.27.19
- By:
- Publication type:
- Article
Adrenocortical carcinoma characterized by gynecomastia: A case report.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 1, p. 9, doi. 10.1297/cpe.27.9
- By:
- Publication type:
- Article
New insights into the pharmacological treatment of pediatric patients with type 2 diabetes.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 1, p. 1, doi. 10.1297/cpe.27.1
- By:
- Publication type:
- Article
Greetings from the JSPE President.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 1, p. 1
- By:
- Publication type:
- Article