Results 301 to 310 of about 4,096,588 (418)

Prenatal diagnosis of omphalocele with extracorporeal liver. [PDF]

open access: yesRadiol Case Rep
Lestari PM   +7 more
europepmc   +1 more source

Value of Magnetic Resonance Spectroscopy for Examining Fetal Brain Development in Mid‐ to Late Pregnancy

open access: yesiRADIOLOGY, EarlyView.
This study demonstrates that the ratio of tNAA to tCr increases during gestation, which correlates with an increase in the number of neurons and cellular energy metabolism in the fetal brain as gestational weeks progress. Additionally, tCho levels exhibit a progressive decrease with advancing gestational weeks, indicating the ongoing development of the
Dejuan Shan   +5 more
wiley   +1 more source

Illuminating Immunity: A Systematic Review of Immune Cell Autofluorescence

open access: yesJournal of Biophotonics, EarlyView.
ABSTRACT Immunophenotyping provides valuable prognostic and diagnostic information, but is technically complex and expensive. The assessment of autofluorescence is label‐free and provides complex information on cell identity. However, research on its application to immunophenotyping has been heterogenous.
Aline Knab   +4 more
wiley   +1 more source

Applying the National Genomic DNA Reference Materials to Evaluate the Performance of Nanopore Sequencing in Identifying Thalassemia Variants

open access: yesJournal of Clinical Laboratory Analysis, EarlyView.
This study mainly to evaluate the performance of nanopore technology in thalassemia detection by utilizing the national genomic reference materials in China. We proved that the reference materials can be used to evaluate the performance of nanopore sequencing in identifying thalassemia mutations, and it's necessary to incorporate triplicates when ...
Xingyu Wei   +7 more
wiley   +1 more source

Prenatal Diagnosis and Clinical Phenotypic Heterogeneity of 22q11.2 Microdeletion Syndrome Based on a Single Center Retrospective Study

open access: yesJournal of Clinical Laboratory Analysis, EarlyView.
Chromosome 22q11.2 microdeletion syndrome (22q11.2DS) is a common congenital disorder with high clinical phenotypic heterogeneity. In this study, we retrospectively investigated the incidence of prenatal diagnosis of 22q11.2DS in a single center and summarized its clinical manifestations to expand the phenotypic database ABSTRACT Objective To ...
Jia‐yan Chen   +2 more
wiley   +1 more source

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