Results 21 to 30 of about 238,616 (363)

Comparative study on optic disc features of premature infants and full‐term newborns

open access: yesBMC Ophthalmology, 2021
Background To study optic disc features of premature infants and compare to that of term infants to explore the pattern and features of newborn optic disc development and provide the basis for the diagnosis of newborn optic disc disease. Methods This was
Xiaofen Feng   +5 more
doaj   +1 more source

Romiplostim use in pregnant women with immune thrombocytopenia

open access: yesAmerican Journal of Hematology, Volume 98, Issue 1, Page 31-40, January 2023., 2023
Abstract Treatment for immune thrombocytopenia (ITP) in pregnancy is hampered by the lack of fetal safety evidence of maternally‐administered medications. The Pregnancy Surveillance Program (PSP) collected patient information from 2017–2020 for pregnancy, birth outcomes, and adverse events (AEs) for 186 women exposed to romiplostim from 20 days before ...
James B. Bussel   +7 more
wiley   +1 more source

Familial Bainbridge‐Ropers syndrome: Report of familial ASXL3 inheritance and a milder phenotype

open access: yesAmerican Journal of Medical Genetics Part A, Volume 191, Issue 1, Page 29-36, January 2023., 2023
Abstract De novo truncating and splicing pathogenic variants in the Additional Sex Combs‐Like 3 (ASXL3) gene are known to cause neurodevelopmental delay, intellectual disability, behavioral difficulties, hypotonia, feeding problems and characteristic facial features.
Schaida Schirwani   +10 more
wiley   +1 more source

Premature Infants Have Normal Maturation of the T Cell Receptor Repertoire at Term

open access: yesFrontiers in Immunology, 2022
Premature infants are known to have immature immune systems compared to term infants; however, the impacts of ex utero immune development are not well characterized.
Sarah U. Morton   +7 more
doaj   +1 more source

Attenuation of the Ganglion Cell Layer in a Premature Infant Revealed with Handheld Spectral Domain Optical Coherence Tomography [PDF]

open access: yes, 2016
Purpose: To report on subclinical retinal abnormalities shown through handheld spectral domain optical coherence tomography on a premature infant. Methods: Case report.
Carroll, Joseph   +3 more
core   +2 more sources

Biallelic GTF2IRD1 variants in brothers with profound neurodevelopmental disorder: A possible novel disorder involving a critical gene for Williams syndrome

open access: yesAmerican Journal of Medical Genetics Part A, Volume 191, Issue 2, Page 332-337, February 2023., 2023
Abstract GTF2IRD1, a gene on chromosome 7 which encodes a transcription factor, is of significant clinical interest due to its heterozygous loss as part of the classical deletion associated with Williams–Beuren syndrome (WBS). However, biallelic variants in GTF2IRD1 alone as part of an autosomal recessive disease have not been previously reported. Here,
Christopher Thomas Cummings   +1 more
wiley   +1 more source

Pengalaman Ibu dalam Merawat Bayi dengan Prematur dan Berat Badan Lahir Rendah

open access: yesNERS Jurnal Keperawatan, 2013
Taking care of the infants becomes a separate stressor especially if the infants is born with premature and infants who have low birth weight. Many problems arise, if the infants is not treated as it should lead to disability and even death.
Deswita
doaj   +1 more source

Inborn Errors of Immunity in the Premature Infant: Challenges in Recognition and Diagnosis

open access: yesFrontiers in Immunology, 2021
Due to heightened awareness and advanced genetic tools, inborn errors of immunity (IEI) are increasingly recognized in children. However, diagnosing of IEI in premature infants is challenging and, subsequently, reports of IEI in premature infants remain ...
Scott M. Gordon, Amy E. O’Connell
doaj   +1 more source

Experiential Learning Care to Increase Maternal Ability in Caring Premature Infants [PDF]

open access: yes, 2016
BACKGROUND: Premature born infants are at high risk for asphyxia, jaundice, and infection. Health care providers and mothers, therefore, should pay more attention to the care of their premature infants.
Binarti, B. (Binarti), Saudah, N. (Noer)
core   +1 more source

The developmental trajectories of the behavioral phenotype and neuropsychiatric functioning in Cornelia de Lange and Rubinstein Taybi syndromes: A longitudinal study

open access: yesAmerican Journal of Medical Genetics Part A, Volume 191, Issue 2, Page 424-436, February 2023., 2023
Abstract Several changes in the behavioral phenotype arise with the growth of children affected by Cornelia de Lange Syndrome (CdLS) and Rubinstein‐Taybi Syndrome (RSTS). However, previous research relied on a cross‐sectional study design turning into age‐related comparisons of different syndromic cohorts to explore age‐dependent changes.
Paola Francesca Ajmone   +11 more
wiley   +1 more source

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