Results 91 to 100 of about 111,118 (342)
ABSTRACT Background Brain development is altered in neonates with congenital heart disease (CHD), with well‐characterised reductions in regional brain volumes and enlargement of CSF spaces. However, perioperative morphological changes remain incompletely understood. Purpose To identify brain regions showing spatial patterns of coordinated expansion and
Mirthe E. M. van der Meijden +14 more
wiley +1 more source
Review of redo-Kasai portoenterostomy for biliary atresia in the transition to the liver transplantation era [PDF]
2017-08Portoenterostomy (PE) is the standard therapy for biliary atresia (BA). PE offers the chance of survival to children with BA. PE was the ultimate therapeutic modality for BA before liver transplantation (LT) was available.
Shirotsuki, Ryo +8 more
core +1 more source
Early discharge after paediatric liver biopsy: A prospective observational study
Abstract Objective To evaluate the safety of early discharge after percutaneous liver biopsy (PLB) in children using prospective bleeding risk stratification. Methods In this prospective observational cohort study, paediatric patients scheduled for PLB were stratified into low‐ and high‐risk groups based on bleeding history and laboratory values.
Fie Brantbjerg Tinning +4 more
wiley +1 more source
Growth and Fibrosis in Children With Biliary Atresia: A Retrospective Cohort Study [PDF]
ABSTRACT Aim To determine growth patterns and catch up potential in children with biliary atresia, in relation to liver disease severity and liver transplantation. Methods This retrospective cohort study was conducted at Copenhagen University Hospital between 1 January 2006 and 31 December 2024 and included 63 children.
Cecilie Lindebjerg +4 more
openalex +2 more sources
Isolated ileocecal valve atresia [PDF]
Ileocecal valve atresia is a rare variety of gastrointestinal atresia. There have been only 10 cases reported in the literature. In this paper, we report the case of a 4-day-old male preterm, who presented with signs of neonatal intestinal obstruction ...
Almaghrebi, Abdulrahman +3 more
core +1 more source
Abstract Objective Pediatric aerodigestive and upper gastrointestinal (UGI) motility disorders are common and may be associated with compromised nutritional status and decreased quality of life. Traditional dietary recommendations for aerodigestive and UGI motility disorders have been rudimentary and largely based upon experience and common sense ...
Khalil El‐Chammas +8 more
wiley +1 more source
AbstrakAtresia bilier merupakan penyakit yang jarang terjadi dan penyababnya belum diketahui secara pasti. Karakteristik dari penyakit ini adalah terjadinya inflamasi progresif pada duktus bilier sehingga terjadi obstruksi ekstrahepatal yang akhirnya ...
Sayoeti, Yorva +2 more
core +1 more source
Abstract Objectives Malnutrition in patients with critical congenital heart disease (CCHD) is associated with worse outcomes, however, feeding challenges, and changes in metabolic demands obscure the relationship between nutrient intake and growth in this patient population.
Colin R. Tang‐Whitmore +8 more
wiley +1 more source
Abstract Objectives Hypertransaminasemia is a frequent finding in hospitalized children with common pediatric illnesses, often considered a transitory phenomenon associated with systemic inflammation/injury. This study aims to assess the prevalence and causes of incidentally detected hypertransaminasemia in children admitted to general pediatric units ...
Angelo Di Giorgio +21 more
wiley +1 more source
An antenatal diagnosis: Congenital high airway obstruction
Congenital high airway obstruction (CHAOS) is a rare lethal fetal malformation characterised by obstruction to the fetal upper airway, which can be partial or complete. Antenatal diagnosis of CHAOS is important due to recent management options. Diagnosis
S Miital +4 more
doaj +1 more source

