Results 251 to 260 of about 1,216,067 (294)

A prediction model for genetic cholestatic disease in infancy using the machine learning approach

open access: yesJournal of Pediatric Gastroenterology and Nutrition, EarlyView.
Diagnostic algorithm for cholestatic infants. Abstract Objectives Cholestasis in infancy poses a complex clinical conundrum for pediatric hepatologists, warranting timely diagnosis, especially for genetic diseases. This study aims to create machine learning (ML)‐based prediction models, referred to as Jaundice Diagnosis Easy for Baby (JADE‐B), to ...
Chi‐San Tai   +9 more
wiley   +1 more source

Protein intake and insulin‐like growth factor‐1 at 12 months and associations with growth, body composition, and metabolic syndrome at 8 years

open access: yesJournal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives Metabolic programming may occur during early life and have long‐lasting effects on metabolic health. This study examined what impact early protein intake and levels of insulin‐like growth factor (IGF‐1) at 1 year of age had on growth, body composition and risk factors for metabolic syndrome at 8 years of age.
Gabriella O. Seidal   +4 more
wiley   +1 more source

Effect of prebiotics on gastrointestinal symptoms and quality of life in children with intestinal failure: A pilot study

open access: yesJournal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives Children with intestinal failure (IF) have a substantial disease burden, with significant gastrointestinal (GI) symptoms, abnormal stool patterns and reduced health‐related quality of life (HRQOL). This study examined the effects of prebiotic supplementation on GI symptoms and HRQOL.
Rut Anne Thomassen   +14 more
wiley   +1 more source

Hereditary hypofibrinogenemia: A rare cause of chronic liver disease

open access: yesJPGN Reports, EarlyView.
Abstract Hypofibrinogenemia is characterized by low levels of fibrinogen with patients commonly presenting asymptomatically. This report discusses a case of hereditary hypofibrinogenemia manifesting as chronic liver disease in a 2‐year‐old male who was evaluated for elevated liver enzymes and skin/soft tissue bleeding.
Hannah Caringal   +4 more
wiley   +1 more source

Transferring an extremely premature infant to an extra-uterine life support system: a prospective view on the obstetric procedure. [PDF]

open access: yesFront Pediatr
van Haren JS   +6 more
europepmc   +1 more source

A case of lactobezoar: Outpatient management in a neonate

open access: yesJPGN Reports, EarlyView.
Abstract A lactobezoar is a conglomerate of undigested and partially digested milk components and is the most common form of bezoar in infants. Described treatments include hospitalization for intravenous fluids and cessation of feeds, endoscopy with administration of N‐acetyl cysteine, and surgical or endoscopic removal.
Shivani Kamal   +3 more
wiley   +1 more source

PEG‐Free Nanoemulsions With Alkyl Polyglucoside and Baccharis dracunculifolia Essential Oil: Physicochemical Behavior, pH Dependence and Skin Repair Properties

open access: yesJournal of Surfactants and Detergents, EarlyView.
ABSTRACT Alkyl polyglucosides (APG) are biodegradable, non‐ionic surfactants from renewable sources with low ecotoxicity. This study developed a novel PEG‐free nanoemulsion (NE) using APG to encapsulate Baccharis dracunculifolia essential oil (BDO) for skin repair.
Carolina Sousa Ponciano   +7 more
wiley   +1 more source

Appendiceal torsion in a premature infant

open access: yesAsian Journal of Surgery
Chao Zheng, Yu Lin, Yifan Fang
doaj   +1 more source

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