Results 91 to 100 of about 24,385 (266)
Tissues obtained from preterm infants with non-inflammatory surgical small intestinal diseases were stained for presence of goblet and Paneth cells. Infants with a diagnosis of IUGR (n = 9) were compared to age-matched non-IUGR infants (n = 4).
Jörn-Hendrik Weitkamp (218989) +6 more
core +1 more source
ABSTRACT Aims and Methods Advances in neonatal care have extended borderline survival to 22–24 post‐conceptional weeks. Present review discusses approaches for prolonging short pregnancies and prevention of serious morbidities in extremely premature infants born before 28 weeks of pregnancy.
Mikko Hallman
wiley +1 more source
Catch-up growth occurs in the IUGR offsprings.
A. Body weights of the controls (CTL) and the IUGR offsprings were recorded at birth (day 0), 2, 7, 14 and 21 days, as well as 2 and 4 months of age. Data are shown as mean ± SD. n = 45; *p .05 vs. CTL. B.
Xinli Wang (300814) +6 more
core +1 more source
ABSTRACT Background Health care financing is thought to be a driver of health care quality. The purpose of this research was to analyze reimbursement for midwifery‐led US birth centers and to evaluate the association between reimbursement ratios and clinical outcomes.
Sarah Bradbury +6 more
wiley +1 more source
Lo IUGR nella nostra popolazione : dati epidemiologici.
Lo IUGR nella nostra popolazione: dati ...
Balestreri D +7 more
core
INTRODUCTION The ATP-binding cassette (ABC) transporter A1 (ABCA1) and ABCG1 are highly expressed in the placenta in various compartments, including the villous syncytiotrophoblast (V-STB) and foetal endothelial cells.
Wenger, F +5 more
core +1 more source
Summary Germline gain‐of‐function variants in sterile alpha motif domain–containing 9‐like (SAMD9L), located on chromosome 7q, cause a multisystem disorder characterized by bone marrow failure, immunodeficiency and variable neurological involvement. Disease evolution is frequently shaped by somatic genetic rescue (SGR), most commonly through monosomy 7,
Hadjer Dellal +10 more
wiley +1 more source
Inhibition of placental mechanistic target of rapamycin (mTOR) signalling, which activates NEDD4-2 (neural precursor cell expressed developmentally down-regulated protein 4-2) ubiquitin ligase leading to increased sodium-coupled neutral amino acid ...
Yi-Yung Chen +5 more
semanticscholar +1 more source
Clinical characteristics of IUGR cases.
Clinical characteristics of IUGR cases.
Gina Capodanno (5029049) +11 more
core +1 more source
USP34 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes
Heterozygous loss‐of‐function variants in USP34 cause a novel neurodevelopmental disorder characterized by global developmental delay, speech impairment, autism, hypotonia, craniofacial dysmorphism, and distal limb anomalies. Disrupted Wnt/β‐catenin signaling via reduced Axin stabilization refines gene‐specific contributions within 2p15p16.1 ...
Helena Wigoda +10 more
wiley +1 more source

