Results 271 to 280 of about 115,582 (346)
Early Kasai portoenterostomy in a 9-day-old newborn with extrahepatic biliary atresia: a case report highlighting improved prognosis with prompt intervention. [PDF]
El-Shabrawi MHF+8 more
europepmc +1 more source
ABSTRACT Background Female infertility is a global health issue however, its link with genital infections is often overlooked due to asymptomatic nature of infections. Delayed diagnosis and treatment due to absence of reliable point‐of‐care (POC) tools result in long‐term pathological consequences and infertility.
Naresh Patnaik+4 more
wiley +1 more source
Circulating Growth Differentiation Factor 15 (GDF15) in Paediatric Disease: A Systematic Review
ABSTRACT Background Growth Differentiation Factor 15 (GDF15), a nonspecific inflammatory marker and member of the TGF‐β superfamily, has a well‐established role in both inflammation and metabolic modulation, but lacks a comprehensive paediatric literature review.
David W. Kronenberger+3 more
wiley +1 more source
Who's afraid of Dura Mater? [PDF]
Zernotti ME, Gavilán J.
europepmc +1 more source
ABSTRACT Preemptive therapy (PET) is safe and effective in controlling Cytomegalovirus (CMV) infection after pediatric liver transplantation (LT) and allows to observe the kinetics of quantitative CMV‐DNA viral load till it reaches the treatment thresholds.
Emanuele Nicastro+15 more
wiley +1 more source
Laparoscopic vs. open portoenterostomy for biliary atresia: a meta-analysis of pediatric surgical outcomes. [PDF]
Zhu J, Wu B, Cai P, Pan J, Zhu Z.
europepmc +1 more source
Review: Hormone Pregnancy Tests Were Teratogenic by the Same Failed Abortion and Hypoxia-Related Mechanism as Misoprostol. [PDF]
Danielsson BR, Ritchie HE.
europepmc +1 more source
Experience in the treatment of type C congenital esophageal atresia using a staged approach. [PDF]
Zhao Y+9 more
europepmc +1 more source
COG6‐related prenatal phenotype (CDG2L): Clinico‐pathological report and review of the literature
Abstract Background CDG2L (MIM#614576) is an autosomal recessive multisystemic disorder due to variants in COG6 gene. Postnatal phenotypes are now well described, while prenatal presentations remain poorly investigated. Only 8 of the 28 published patients have had prenatal ultrasound anomalies reported and no one post‐mortem investigation.
Sarah Guterman+17 more
wiley +1 more source