International Journal of Pediatric Endocrinology
Overview
International Journal of Pediatric Endocrinology is a scientific journal, published by Biomed Central since 2009 in English. The journal's country of origin is United Kingdom and its primary focus area is pediatrics.
Details
Details
Abbr.
Int J Pediatr Endocrinol
Publisher
Biomed Central
Start
2009
End
2020
Frequency
Quarterly
p-ISSN
1687-9848
e-ISSN
1687-9856
Country
United Kingdom
Language
English
Specialty
Pediatrics
Recent Articles
1.
Angulo M, Abuzzahab M, Pietropoli A, Ostrow V, Kelepouris N, Tauber M
Int J Pediatr Endocrinol
. 2020 Dec;
2020(1):20.
PMID: 33292530
Background: Growth hormone (GH) deficiency is common in patients with Prader-Willi syndrome (PWS) and leads to short adult stature. The current study assessed clinical outcomes based on real-world observational data...
2.
Omar A, Nyaga G, Mungai L
Int J Pediatr Endocrinol
. 2020 Dec;
2020(1):22.
PMID: 33292495
Background: Gonadotropin releasing hormone agonists (GnRHa) are well established as a standard of care for the treatment of central precocious puberty (CPP) worldwide. While numerous delivery systems and routes of...
3.
Musa S, Ibrahim A, Hassan S, Johnson M, Basheer A, Arabi A, et al.
Int J Pediatr Endocrinol
. 2020 Dec;
2020(1):21.
PMID: 33292488
Background: Fanconi-Bickel syndrome (FBS) is a rare condition of carbohydrate metabolism, caused by a recessive defect in the facilitative glucose transporter GLUT2 encoded by the SLC2A2 gene and characterized by...
4.
Miller B, Ross J, Ostrow V
Int J Pediatr Endocrinol
. 2020 Oct;
2020:19.
PMID: 33042202
Background: Treatment of children with growth hormone deficiency (GHD) or idiopathic short stature (ISS) using GH is only effective for bone growth prior to epiphyseal fusion. Aromatase inhibitor therapy (AIT)...
5.
Bonouvrie K, Van Der Werff Ten Bosch J, van den Akker M
Int J Pediatr Endocrinol
. 2020 Oct;
2020:18.
PMID: 33005196
Objective: The most common presentation of Klinefelter syndrome (KS) is infertility and features of hypogonadism. Currently no consensus exists on the risk of malignancy in this syndrome. Several case reports...
6.
Gujral J, Costin G, Khurana D, Yau M, Wallach E, Romero C, et al.
Int J Pediatr Endocrinol
. 2020 Sep;
2020:16.
PMID: 32944019
Background: Antifungals act on fungal sterols structurally similar to human cholesterol. Ketoconazole reversibly suppresses steroidogenesis by inhibiting cytochrome P450 enzymes and interferes with dihydrotestosterone (DHT) activity by binding to the...
7.
Yau D, Marwaha R, Mohnike K, Sajjan R, Empting S, Craigie R, et al.
Int J Pediatr Endocrinol
. 2020 Sep;
2020:17.
PMID: 32874187
Background: Congenital Hyperinsulinism (CHI) is an important cause of severe hypoglycaemia in infancy due to excessive, dysregulated insulin secretion. In focal CHI, a localised lesion within the pancreas hypersecretes insulin...
8.
Lim W, Germain-Lee E, Dunbar N
Int J Pediatr Endocrinol
. 2020 Aug;
2020:15.
PMID: 32782451
Background: Acrodyostosis type 1 (ACRDYS1) is a rare skeletal dysplasia, and sometimes it can be misdiagnosed as pseudohypoparathyroidism type 1A (PHP1A), a subtype of Albright hereditary osteodystrophy (AHO), due to...
9.
Van Vlaenderen J, Logghe K, Schiettecatte E, Vermeersch H, Huvenne W, De Waele K, et al.
Int J Pediatr Endocrinol
. 2020 Jul;
2020:14.
PMID: 32699545
Case Presentation: We report for the first time a synchronous papillary and follicular thyroid carcinoma in a 12-year-old girl presenting with a large (5 cm diameter) left thyroid nodule, an...
10.
Tung J, Lai S, Au S, Yeung K, Kan A, Loong F, et al.
Int J Pediatr Endocrinol
. 2020 Jul;
2020:13.
PMID: 32670376
Background: Beckwith-Wiedemann syndrome (BWS) is an overgrowth syndrome with variable clinical phenotype and complex molecular aetiology. It is mainly caused by dysregulation of the chromosome 11p15 imprinted region, which results...