Longitudinal changes in nonfunctioning pituitary neuroendocrine tumors in children receiving growth hormone therapy: A comparison with untreated patients [0.03%]
生长激素治疗儿童非功能性垂体神经内分泌肿瘤的纵向变化与未治疗患者的比较研究
Yasemin F Bahar,Kürşat Çetin,Zeynep Donbaloğlu et al.
Yasemin F Bahar et al.
Background: Growth hormone deficiency (GHD) may result from structural abnormalities or space-occupying lesions of the pituitary gland; therefore, pituitary magnetic resonance imaging (MRI) is routinely performed as part of the etiological ...
Anemia and iron deficiency in healthy, exclusively breastfed infants: Prevalence and association with sex and birth weight [0.03%]
健康、纯母乳喂养婴儿的贫血和缺铁现状及其与性别和出生体重的关系
Ana Varea,Liliana Disalvo,Marisa Sala et al.
Ana Varea et al.
Introduction. Anemia and iron deficiency (ID) negatively affect health and neurocognitive development. There is controversy over whether breast milk meets iron requirements between four and six months of age, especially in populations with ...
Incidence and epidemiology of pediatric acute respiratory distress syndrome in Argentina: Secondary analysis of data from the International PARDIE Study [0.03%]
阿根廷儿童急性呼吸窘迫综合征的发病及流行病学特征：国际PARDIE研究的二次分析数据
Matías G Herrera,Luis H Llano López,Analía Fernández et al.
Matías G Herrera et al.
Introduction. Pediatric acute respiratory distress syndrome (PARDS) poses a clinical challenge due to its highmorbidityandmortality.Specific diagnostic criteriaexistforthepediatricpopulation;however,evidence in our setting is limited. The o...
Correlation of MTHFR (methylenetetrahydrofolate reductase) gen polymorphism, folate and neonatal hyperbilirubinemia [0.03%]
亚甲基四氢叶酸还原酶基因多态性、叶酸与新生儿高胆红素血症的关系研究
Zhen Zhang,Weifeng Bai,Youhong Duan et al.
Zhen Zhang et al.
Objective. Investigate the distribution of methylenetetrahydrofolate reductase (MTHFR) genotypes in newborns with hyperbilirubinemia and explore their correlation with folate concentration and bilirubin elevation. Methods. Neonates with hyp...
[Neurofibromatosis Type 1 in Pediatrics: Recommendations for Diagnosis and Management] [0.03%]
儿童神经纤维瘤病1型的诊断和治疗建议
Rosana M Flores,Paola A Clerico Mosina,Cecilia I Crowe et al.
Rosana M Flores et al.
Neurofibromatosis type 1 (NF1) is the most prevalent neurocutaneous syndrome, affecting approximately 1 in 3000 individuals. This genetic disorder involves multiple organ systems and exhibits marked variability in clinical presentation, wit...
Diagnostic accuracy of presepsin and C-reactive protein in the early stages of neonatal sepsis: A prospective study [0.03%]
降钙素原和C-反应蛋白在新生儿早期感染性肺炎诊断中的准确性：一项前瞻性研究
Carolina Giudice,María F Galletti,Graciela B Jiménez et al.
Carolina Giudice et al.
Introduction. Neonatal sepsis is a common complication in the neonatal intensive care unit (NICU). Biomarkers have certain limitations, and recent studies suggest that presepsin (PSEP) could be used for early diagnosis. Objective. To determ...
Vesicoureteral reflux in children with urinary tract infections caused by atypical pathogens: Diagnostic accuracy of renal ultrasound [0.03%]
由非典型病原体引起的儿童泌尿系感染的肾超声诊断价值及反流发生率研究
Milena Rivero Segura,Andrés E Cabal Álvarez,Lucía D&#x;Ambrosio et al.
Milena Rivero Segura et al.
Introduction. The need to perform voiding cystourethrography (VCUG) in patients with a first episode of urinary tract infection (UTI) caused by atypical pathogens is controversial. The primary objective of this study was to evaluate the dia...
Malnutrition and hypernatremic dehydration as the initial presentation of nephrogenic diabetes insipidus in an infant [0.03%]
小儿尿崩症合并营养不良和高钠血症的临床表现病例报告
Micaela Valdez,María A Quiroga Viola,Rosario Flores et al.
Micaela Valdez et al.
Congenital nephrogenic diabetes insipidus (CNDI), also known as arginine vasopressin resistance, is a rare inherited disorder of water homeostasis in which the kidneys lose their ability to concentrate urine, leading to polyuria, polydipsia...