Results 171 to 180 of about 754,434 (404)

Nurses Lived Experiences in Neonatal Intensive Care Units [PDF]

open access: yes, 2013
Advanced technology is saving infants at earlier stages often only to see them die agonizing deaths or face lifetime infirmities. In this phenomenological study, 16 NICU nurses provided their experiences dealing with these patients, their families and ...
Passmore, Denise
core  

The prevalence of hearing loss in infants hospitalized in the neonatal intensive care units

open access: diamond, 2020
Nasrin Gohari   +5 more
openalex   +1 more source

THE “PANEL PARENT” AS AN ADJUNCT TO THE SPECTRUM OF NEONATAL INTENSIVE CARE [PDF]

open access: bronze, 1977
Gilbert I. Martin   +6 more
openalex   +1 more source

Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat   +4 more
wiley   +1 more source

Effect of in-line filtration in newborns: study protocol of the Intravenous Neonatal Central Access Safety (INCAS) randomized controlled trial

open access: yesTrials
Background Particulate contamination due to infusion therapy (administration of parenteral nutrition and medications) carries a potential health risk for infants in neonatal intensive care units (NICUs). This particulate consists of metals, drug crystals,
Francesco Cresi   +10 more
doaj   +1 more source

Long‐Read Genome Sequencing Establishes Biallelic Pathogenic Variants in DNM1 With Distinct Functional Effects as the Cause of Early Infantile Developmental and Epileptic Encephalopathy

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous de novo and inherited biallelic pathogenic variants in DNM1 have been reported in association with autosomal dominant (AD) and autosomal recessive (AR) developmental and epileptic encephalopathy, respectively, due to aberrant dynamin function or expression, with each inheritance pattern associated with a different mechanism of ...
Andy Drackley   +7 more
wiley   +1 more source

Stressors of Parents of Hospitalized Preterm Infants: a study in Neonatal Intensive Care Unit of Afzalipour Hospital, Kerman, Iran [PDF]

open access: yes, 2015
Background: Birth is a pleasant event, but premature birth and subsequently neonate hospitalization in the neonatal intensive care unit, is stressful for parents.
Baniasadi, Hamideh   +2 more
core  

KDM2B‐Related Neurodevelopmental Disorder A Case‐Series Supporting the CxxC Domain Phenotype With Emphasis on Ocular and Dermatologic Features

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The KDM2B‐related neurodevelopmental disorder is a recently identified Mendelian disorder of the epigenetic machinery associated with pathogenic variants in KDM2B. Global developmental delay, intellectual disability, congenital anomalies, and systemic manifestations characterize the disorder.
Adriana Gomes   +3 more
wiley   +1 more source

The effects of maternal voice on pain during placement of peripherally inserted central catheter in neonates

open access: yesFrontiers in Pain Research
BackgroundPeripherally inserted central catheter (PICC) are a necessary procedure for preterm newborns care. Despite the use of analgesic treatments, its insertion can be painful.
Audrey Flours   +10 more
doaj   +1 more source

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