Results 191 to 200 of about 114,602 (311)

Congenital ileal stenosis. [PDF]

open access: yesJ Surg Case Rep
Wang M, Lindholm EB.
europepmc   +1 more source

Most costly and prevalent reasons for hospitalization in children with medical complexity in Ontario, Canada

open access: yesJournal of Hospital Medicine, Volume 21, Issue 5, Page 495-505, May 2026.
Abstract Background and Objectives Children with medical complexity (CMC) have chronic health conditions often associated with functional limitations. CMC comprise 1%–5% of the pediatric population. In Canada, their care accounts for one‐third of pediatric health spending.
Erin Hessey   +25 more
wiley   +1 more source

Closing/Closed Gastroschisis (CGS): Antenatal Predictors and Surgical Strategies in Cases of Unique Anatomy from a Case Series. [PDF]

open access: yesChildren (Basel)
Morozov D   +8 more
europepmc   +1 more source

Breastmilk and medium‐chain triglyceride supplementation: Retrospective study on outcomes in biliary atresia infants after Kasai

open access: yesJournal of Pediatric Gastroenterology and Nutrition, Volume 82, Issue 5, Page 1269-1277, May 2026.
Does breastmilk with medium‐chain triglycerides (MCT) after Kasai support growth and improve surgical outcomes? Abstract Objective To relate post‐surgical feeding regimens to growth and surgical outcomes in children with biliary atresia (BA) after hepato‐portoenterostomy (Kasai).
Thora Wesenberg Helt   +6 more
wiley   +1 more source

Notes on reproduction of the Sierra Nevada yellow-legged frog from California

open access: yesCalifornia Fish and Wildlife Journal, 2020
Stephen R. Goldberg
doaj   +1 more source

Usefulness of Transparent Illumination Device in Esophageal Atresia for the Detection of the Distal Esophagus. [PDF]

open access: yesSurg Case Rep
Uematsu Y   +6 more
europepmc   +1 more source

Frequent achievement of a drug-free state after orthotopic liver transplantation [PDF]

open access: yes, 1993
Abu-Elmagd, K   +11 more
core  

Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea

open access: yesJPGN Reports, Volume 7, Issue 2, Page 242-246, May 2026.
Abstract Among congenital diarrhea and enteropathies (CODEs), proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency is a rare monogenic disorder, associated with severe neonatal diarrhea and polyendocrinopathies. We report an 18‐day‐old male neonate, born to consanguineous parents, presenting with persistent watery diarrhea, metabolic ...
Eleonora Saraceno   +7 more
wiley   +1 more source

Age at First RSV Hospitalisation and the Risk of Subsequent Bacterial Pneumonia

open access: yes
Acta Paediatrica, Volume 115, Issue 6, Page 1298-1300, June 2026.
Samuel Videholm   +4 more
wiley   +1 more source

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