Results 61 to 70 of about 691,015 (282)
As a novel adipose‐derived neurotrophic factor, Follistatin‐like 1 is endocytosed by sympathetic neurons primarily via tropomyosin‐related kinase B. This process promotes sympathetic innervation in adipose tissue and norepinephrine release, leading to white adipose tissue browning, enhanced thermogenesis, and anti‐obesity effects in mice.
Xiao‐Wei Jia +13 more
wiley +1 more source
Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects
ABSTRACT LRP1 encodes the low‐density lipoprotein (LDL) receptor‐related protein 1 (LRP1), a transmembrane protein involved in endocytosis and activation of multiple signaling pathways. LRP1 variants have been implicated in the pathogenesis of congenital heart defects (CHD), Alzheimer's disease, and neurodevelopmental disorders (NDD).
Alyssa L. Rippert +31 more
wiley +1 more source
Treatment of a Gastric Lactobezoar with N-Acetylcysteine
Lactobezoars are a rare finding with potentially serious sequelae in pediatric patients with feeding intolerance. Aggressive treatment may be preferred to traditional treatments to avoid complications in medically complex patients.
Brandon Sparks, Anil Kesavan
doaj +1 more source
Feeding difficulty has been reported at a higher incidence in infants with cyanotic heart disease and single ventricle physiology necessitating specialized feeding strategies.
Nayan T Srivastava +2 more
doaj +1 more source
ABSTRACT Microdeletions impacting 15q11.2 breakpoint (BP) 1 to BP2, adjacent to the Prader–Willi critical region, have previously described neuropsychiatric associations, with potential low penetrance presentations of congenital heart disease (CHD) also identified.
Morgan B. Wright +10 more
wiley +1 more source
Patient and Family Reported Clinical Picture of IRF2BPL‐Related Disorders
ABSTRACT IRF2BPL‐related disorder is a neurodevelopmental disorder caused by heterozygous variants in the IRF2BPL (Interferon Regulatory Factor 2 Binding Protein‐Like) gene. The few reports available in the literature suggest that common symptoms include developmental delay, intellectual disability, and developmental regression.
Zoe Goldstone‐Joubert +4 more
wiley +1 more source
Understanding of Pathophysiological Basis of Feeding Intolerance in Critically ill Children
Children with critical illnesses are at increased risk for intestinal injury, gastrointestinal dysfunction, and feeding intolerance, which are associated with delayed recovery and increased morbidity and mortality during their course in the pediatric ...
Soyhan Bağcı +2 more
doaj +1 more source
Rethinking brachycephaly: Anatomical implications and health considerations in lagomorphs
Abstract Brachycephaly in domestic rabbits is increasingly perceived by welfare organizations as associated with significant health complications, particularly oral pathologies. Despite this perception, comparative anatomical research into rabbit brachycephaly is limited compared to that of dogs and cats, compelling an in‐depth examination of its ...
Helaina Cressy +3 more
wiley +1 more source
Construction and validation of a predictive model for the risk of feeding intolerance to enteral nutrition therapy in HIV/AIDS patients [PDF]
Objective To investigate the influencing factors of enteral nutrition therapy intolerance in HIV/AIDS patients, establish and validate a Nomogram model.Methods A retrospective analysis was conducted on the clinical data of hospitalized HIV/AIDS patients ...
GONG Beibei +4 more
doaj +1 more source
Nasogastric feeding intolerance in the critically ill [PDF]
The aims of this study were to determine when patients develop feed intolerance, the prevalence of feed intolerance in subgroups, and other factors that influence feed intolerance. Nasogastric delivery of nutrition commonly fails in critically ill patients.
OConnor, S +8 more
openaire +1 more source

