Results 141 to 150 of about 98,806 (349)

Mortality and Neurodevelopmental Outcome in an Italian Cohort of Very Low Birth Weight Infants

open access: yesActa Paediatrica, EarlyView.
ABSTRACT Aim Preterm infants face high risks of mortality and neurodevelopmental impairment. We aimed to evaluate the outcomes in an Italian cohort of very low birth weight infants. Methods This multicenter prospective study included very low birth weight infants born in Italy between 2016 and 2020. Severe functional disability was defined as cognitive
Lugli Licia   +28 more
wiley   +1 more source

Chylothorax after patent ductus arteriosus ligation in a dog with persistent left cranial vena cava

open access: yesAustralian Veterinary Journal, EarlyView.
This report is the first to document chylothorax after patent ductus arteriosus (PDA) ligation in a dog with a persistent left cranial vena cava (PLCVC), highlighting potential complications arising from concurrent cardiovascular anomalies. A nine‐month‐old female desexed Pomeranian was referred for PDA. Echocardiography confirmed a left‐to‐right shunt
TR Nash, GL Hosgood
wiley   +1 more source

Анатомы - лечащие врачи папства (обзор литературы) [PDF]

open access: yes, 2013
Стаття присвячена анатомам, які були особистими лікарями Пап Римських у різний час: М. Р. Коломбо (1515-1559), Г. Б. Канано (1515-1579), Г. C. Аранзі (1530-1589), К. Варолій (1543- 1575), А. Чезальпіно (1525-1603), М. Мальпігі (1628-1694), Дж.
Kutya, S.A., Melnik, M.V., Schvets, T.A.
core  

Six New Cases of 22q13.2 Gain Including TFC20: First Report of Triplication and Smallest Duplication Associated With Neurodevelopmental Delays

open access: yesClinical Genetics, EarlyView.
This study reports six new cases of 22q13.2 duplication and triplication, including the TCF20 gene, associated with neurodevelopmental disorders and various morphological and systemic abnormalities. The findings suggest a variable expressivity, but their complete penetrance remains uncertain compared to well‐established loss‐of‐function variants ...
Etienne Bizot   +13 more
wiley   +1 more source

The Phenotypic Spectrum of Miller Syndrome: Insight From a French Cohort

open access: yesClinical Genetics, EarlyView.
This study expands the clinical spectrum of Miller syndrome by reporting novel features including preaxial defects, facial nevus simplex, and optic atrophy. It also includes the first patients with homozygous DHODH variants, emphasizing the importance of early diagnosis and the variability of presentations, from severe prenatal to mild adult phenotypes.
Marion Aubert Mucca   +13 more
wiley   +1 more source

Predictive Performance of Device‐Neonatal Skin Risk Assessment Scale to Evaluating Pressure Injuries Risk in the Neonates. An Observational Multicenter Study

open access: yesJournal of Clinical Nursing, EarlyView.
ABSTRACT Aim To assess the validity of a modified Neonatal Skin Risk Assessment scale (Dev‐NSARS) for neonatal pressure injuries (PIs) in the neonatal intensive care unit (NICU) and neonatal sub‐intensive care unit (NICU‐Sub) environment. Background Medical devices are the leading cause of pressure injuries (PIs) in neonates, a key cause of morbidity ...
Biagio Nicolosi   +6 more
wiley   +1 more source

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