Clinical Pediatric Endocrinology : Impact Factor & More
eISSN: 1347-7358pISSN: 0918-5739
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Key Metrics
CiteScore 
1.9
H-Index
19
SJR
Q2Endocrinology
SNIP
0.79
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Topics Covered on Clinical Pediatric Endocrinology
Clinical Pediatric Endocrinology Journal Specifications
Indexed in the following public directories
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Scopus 
SJR
| Overview | |
| Publisher | JAPANESE SOC PEDIATRIC ENDOCRINOLOGY |
| Language | English |
| Frequency | Quarterly |
| General Details |
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Recently Published Papers in Clinical Pediatric Endocrinology
Uterine artery pulsatility index as a functional biomarker of centralprecocious puberty: a scoping review
- 1 Jul 2026
- Clinical Pediatric Endocrinology
Molecular modeling and clinical characterization of a CYP17A1 variant(p.Asp298Asn) causing 17\u03b1-hydroxylase/17,20-lyase deficiency in twosiblings
- 5 May 2026
- Clinical Pediatric Endocrinology
Perinatal hypophosphatasia refractory to asfotase alfa with neutralizingantibodies that affected bone mineralization: a case report
- 20 Apr 2026
- Clinical Pediatric Endocrinology
A case of familial isolated hypoparathyroidism type 2 with novel compoundheterozygous variants in GCM2
- 19 Apr 2026
- Clinical Pediatric Endocrinology
PTHLH gene variant in an Indian boy withbrachydactyly type E: A case report and literature review
- 14 Apr 2026
- Clinical Pediatric Endocrinology
Efficacy and safety of GH treatment in Japanese pediatric patients withSHOX deficiency: an open-label extensionstudy
- 10 Apr 2026
- Clinical Pediatric Endocrinology
Uterine artery pulsatility index as a functional biomarker of centralprecocious puberty: a scoping review
- 1 Jul 2026
- Clinical Pediatric Endocrinology
Molecular modeling and clinical characterization of a CYP17A1 variant(p.Asp298Asn) causing 17\u03b1-hydroxylase/17,20-lyase deficiency in twosiblings
- 5 May 2026
- Clinical Pediatric Endocrinology
Perinatal hypophosphatasia refractory to asfotase alfa with neutralizingantibodies that affected bone mineralization: a case report
- 20 Apr 2026
- Clinical Pediatric Endocrinology
A case of familial isolated hypoparathyroidism type 2 with novel compoundheterozygous variants in GCM2
- 19 Apr 2026
- Clinical Pediatric Endocrinology
PTHLH gene variant in an Indian boy withbrachydactyly type E: A case report and literature review
- 14 Apr 2026
- Clinical Pediatric Endocrinology
Efficacy and safety of GH treatment in Japanese pediatric patients withSHOX deficiency: an open-label extensionstudy
- 10 Apr 2026
- Clinical Pediatric Endocrinology
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