Metreleptin treatment for congenital generalized lipodystrophy type 4 (CGL4): a case report
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.1
Immune checkpoint inhibitor therapy for pediatric cancers: A mini review of endocrine adverse events
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.59
Long-term care, from neonatal period to adulthood, of children born small for gestational age
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.97
Autosomal dominant Hashimoto’s thyroiditis with a mutation in TNFAIP3
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.91
Prediction and prevention of type 1 diabetes in children
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.43
Recent advances in research on isolated congenital central hypothyroidism
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.69
Combination therapy of propranolol, levothyroxine, and liothyronine was effective in a case of severe consumptive hypothyroidism associated with infantile hepatic hemangioma
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.9
Comprehensive medical treatment of women with Turner syndrome may improve pregnancy outcomes: A case report
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.37
Levothyroxine dosages less than 2.4 μg/kg/day at 1 year and 1.3 μg/kg/day at 3 years of age may predict transient congenital hypothyroidism
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.127
The long-term management of congenital generalized lipodystrophy (Berardinelli-Seip syndrome): the clinical manifestations of Japanese siblings for approximately 20 years
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.139
MIRAGE syndrome with recurrent pneumonia probably associated with gastroesophageal reflux and achalasia: A case report
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.147
A case of pseudohypoparathyroidism type Ia with a novel frameshift mutation in the GNAS gene: early diagnosis of osteoma cutis by skin biopsy
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.15
Treatment of adrenal crisis in patients with primary hypoadrenalism can lead to hypertension
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.25
Gonadal failure among female patients after hematopoietic stem cell transplantation for non-malignant diseases
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.105
Frequent and prolonged administration of glucocorticoid for acute adrenal insufficiency treatment can cause diabetes mellitus: A case of holoprosencephaly
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.31
Novel AVPR2 variant in a male infant with nephrogenic diabetes insipidus who showed delayed head control
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.155
Uterus in mixed gonadal dysgenesis was detected by continuous irregular vaginal bleeding
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.135
Rapid increase in the incidence of end-stage renal disease in patients with type 1 diabetes having HbA1c 10% or higher for 15 years
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.113
A Japanese case of familial hypercholesterolemia with a novel mutation in the LDLR gene
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.19
Identifying a risk score for childhood obesity based on predictors identified in pregnant women and 1-year-old infants: An analysis of the data of the Hokkaido Study on Environment and Children’s Health
来源期刊:Clinical Pediatric EndocrinologyDOI:10.1297/cpe.28.81