Results 221 to 230 of about 1,324,038 (335)

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

Foveal Identification and Development in Prematurity-Implications on Zone Localization and Nutritional Supplementation. [PDF]

open access: yesInvest Ophthalmol Vis Sci
Shah SV   +7 more
europepmc   +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

Social determination in the health of children born preterm: a scoping review. [PDF]

open access: yesRev Lat Am Enfermagem
Soares MFMR   +5 more
europepmc   +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

Incubators for Premature Infants

open access: yesAmerican Journal of Public Health and the Nations Health, 1940
Juanita Witters   +3 more
openaire   +4 more sources

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