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期刊名:Clinical pediatric endocrinology

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ISSN:0918-5739

e-ISSN:1347-7358

IF/分区:1.0/Q4

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Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Takeshi Yamaguchi,Naomi Tamura,Hiroyoshi Iwata et al. Takeshi Yamaguchi et al.
Growth charts are essential tools for monitoring the physical development of children. We analyzed data from a nationwide Japanese birth cohort of 98,987 participants to create eight growth charts stratified by birth weight in 500-gram incr...
Mario Daniel Caba-Flores,Cesar Huerta-Canseco,Carmen Martínez-Valenzuela et al. Mario Daniel Caba-Flores et al.
Adipocytokines are proteins with systemic metabolic effects, and additional adipocytokines have been identified. Adipocytokines are present in the serum, and obesity-mediated inflammation can alter their expression. Breast milk also contain...
Daly Pen,Kimyi Phou,Sokuntheavy Ly et al. Daly Pen et al.
Neonatal hyperthyroidism (NH) mostly commonly occurs in infants born to mothers with Graves' disease. NH in extremely low birth weight (ELBW) infants has been rarely described. Here, we report a case of NH in an infant born at 29 wk 6 d of ...
Kentaro Kishi,Shun Soneda,Takahiro Mochizuki et al. Kentaro Kishi et al.
This study compared the age at onset of puberty among boys with short stature (prepubertal height SD score (SDS) ≤ -2.0 SD) who were small-for-gestational age (SGA) and those who were appropriate-for-gestational age (AGA), as well as healt...
Arindam Ghosh,Saba Annigeri,Chakita Singh et al. Arindam Ghosh et al.
Allgrove syndrome (AS), an uncommon multisystem disorder, is characterized by the classic clinical triad of alacrimia, achalasia, and adrenal insufficiency, and is typically limited to glucocorticoid deficiency with preserved mineralocortic...
Erika Uehara,Keiichi Sugihara,Ikue Hata et al. Erika Uehara et al.
KCNJ11 is one of the major causative genes for congenital hyperinsulinism (CHI) characterized by neonatal and infantile hypoglycemia. Although one readthrough KCNJ11 variant has been identified in a patient with CHI, the pathogenicity of th...
Keiko Nagahara,Sakura Motegi,Ayako Ochi et al. Keiko Nagahara et al.
Advanced glycation end-products (AGEs) formed by non-enzymatic glycation reactions between sugars and proteins have been implicated in various age-related disorders. Skin autofluorescence (SAF) is a noninvasive method for estimating the acc...
Sayuri Koizumi,Ikuma Musha,Koichi Toda et al. Sayuri Koizumi et al.
Congenital hyperinsulinism (CHI) is characterized by hypoglycemia caused by excessive insulin secretion. CHI is classified into two types: transient CHI, which resolves within 3-4 mo of birth, and persistent CHI, which persists beyond this ...