Results 211 to 220 of about 392,221 (346)

Unexplained gut symptoms in extremely preterm infants are associated with gastrointestinal dysfunction at 5.5 years

open access: yesActa Paediatrica, EarlyView.
Abstract Aim To evaluate whether extremely preterm infants with considerable gastrointestinal (GI) symptoms during the neonatal period, but without major abdominal surgery or necrotising enterocolitis, had an increased probability of developing GI dysfunction later in life.
Júlíus Kristjánsson   +3 more
wiley   +1 more source

Management of Neonatal Hyperglycaemia in Sweden—A Survey Study

open access: yesActa Paediatrica, EarlyView.
ABSTRACT Aim Neonatal hyperglycaemia is associated with a multitude of adverse outcomes, including mortality and impaired neurological development. The aim of this study was to characterise the current management of neonatal hyperglycaemia in Swedish neonatal units.
Ludvig Henriksson Frithiof   +2 more
wiley   +1 more source

Intestinal-Failure-Associated Liver Disease: Beyond Parenteral Nutrition. [PDF]

open access: yesBiomolecules
Mignini I   +11 more
europepmc   +1 more source

Neonatal Inflammation and Feeding Disorders at 1 Year in Infants With Congenital Gastrointestinal Malformations

open access: yesActa Paediatrica, EarlyView.
ABSTRACT Aim To investigate the associations between inflammatory markers and the risk of paediatric feeding disorders (PFD) at 1 year of age in infants with congenital gastrointestinal malformations (CGMs). Methods Neonates with CGMs admitted to our NICU and prospectively followed up in our outpatient clinic were included.
Cristina Mastropietro   +7 more
wiley   +1 more source

Approach to the Management of Gastrointestinal Manifestations in Patients With Phaeochromocytoma and Paraganglioma

open access: yesClinical Endocrinology, EarlyView.
ABSTRACT Objective Managing gastrointestinal symptoms in patients with phaeochromocytoma and paraganglioma (PPGL) is challenging due to the risk of catecholaminergic crisis with many commonly prescribed medications, especially in functional tumours.
Monica Majumder   +5 more
wiley   +1 more source

The Impact of Long-Term Parenteral Nutrition on Physical Development and Bone Mineralization in Children with Chronic Intestinal Failure. [PDF]

open access: yesNutrients
Romanowska H   +9 more
europepmc   +1 more source

Pathogenic Deep Intronic PCSK1 Variant Causes Proprotein Convertase 1/3 Deficiency in a Family

open access: yesClinical Genetics, EarlyView.
Biallelic PCSK1 loss‐of‐function mutations cause proprotein convertase 1/3 (PC1/3) deficiency, a polyendocrinopathy; a total of 36 patients were reported. The first deep intronic PCSK1 variant, (NM_000439.5):c.1196+2681T>A, was found to segregate with the disease in a consanguineous family, and is shown together with 32 reported mutations.
Leah M. Huber   +6 more
wiley   +1 more source

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