Results 141 to 150 of about 48,998 (266)

Managing Pregnancy in Inherited Metabolic Disorders: Experience From a Single Tertiary Metabolic Center. [PDF]

open access: yesJ Obstet Gynaecol Res
İşler-Soylu E   +7 more
europepmc   +1 more source

The genetic landscape of congenital diarrheas and very early onset inflammatory bowel disease in the Middle East

open access: yesJPGN Reports, EarlyView.
Abstract Objectives Monogenic causes of congenital diarrheas and enteropathies (CoDE) and very early onset inflammatory bowel disease (VEOIBD) are mostly recessive and therefore more prevalent in populations with increased consanguinity rates. To assess the genetic basis of these disorders in a likely high‐prevalence population, we established a multi ...
Lily Gillette   +21 more
wiley   +1 more source

Congenital short bowel syndrome: Clinical aspects by systematic review

open access: yesJPGN Reports, EarlyView.
Abstract Objectives Congenital short bowel syndrome (CSBS) is a rare intestinal disorder characterized by inborn shortening of the bowel with mainly mutations in Coxsackie and Adenovirus receptor‐like membrane protein (CLMP) and Filamin A (FLNA) genes.
Barblin Remund   +2 more
wiley   +1 more source

New Perspectives in Nutritional Management for Neonatal Health. [PDF]

open access: yesNutrients
Salvatore S   +3 more
europepmc   +1 more source

Shaping the research agenda of pediatric gastroenterology, hepatology, and nutrition: The proposal from an Italian Society of Pediatric Gastroenterology, Hepatology and Nutrition (SIGENP) expert group

open access: yesJPGN Reports, EarlyView.
Abstract The Italian Society of Pediatric Gastroenterology, Hepatology and Nutrition (SIGENP) recognized the need to define research priorities and identify knowledge gaps to guide future investigations in pediatric digestive health. Following international examples, SIGENP aimed to provide a structured framework that aligns scientific innovation with ...
Carlo Agostoni   +46 more
wiley   +1 more source

Reversal of surgical biliary diversion with ileal bile acid transport inhibitors: A new chapter in progressive familiar intrahepatic cholestasis type 1 management?

open access: yesJPGN Reports, EarlyView.
Abstract Progressive Familial Intrahepatic Cholestasis type 1 (PFIC1) is a multisystem disorder. Although liver transplant (LT) resolves the hepatic disease, post‐LT complications may occur, including severe enteropathy and graft steatosis caused by impaired bile acids handling by the native intestine.
Teresa Botelho   +6 more
wiley   +1 more source

Microbial shifts in early life: the pediatric gut microbiome and its role in health and disease. [PDF]

open access: yesGut Microbes
Waghmode S   +4 more
europepmc   +1 more source

Chronic nutritional disorders in the infant.

open access: yesArchivos de pediatria del Uruguay, 2007
A, ARIZTIA, T, ZENTENO
openaire   +1 more source

Home - About - Disclaimer - Privacy