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...
Sabrina Merenzon,Paula C Luna,María E Abad et al.
Sabrina Merenzon et al.
Pediatric psoriasis accounts for approximately 2% of dermatological conditions in children under 16 years of age. The objective of this study is to describe the clinical characteristics, treatment regimens, and observed efficacy and safety ...
María S Ciruzzi
María S Ciruzzi
Andrea Exeni
Andrea Exeni
Primary ciliary dyskinesia: Clinical and tomographic characterization using a combined diagnostic approach [0.03%]
纤毛不动综合征的临床及影像学特征研究：综合诊断方法的应用
Juan E Balinotti,Martín Medin,Ángela Lacera Rincón et al.
Juan E Balinotti et al.
Introduction. Primary ciliary dyskinesia (PCD) is a clinically heterogeneous condition that is difficult to diagnose. This study aimed to describe the clinical and imaging characteristics and the results of diagnostic tests in patients with...