Results 31 to 40 of about 58,515 (333)

Single umbilical artery

open access: hybrid, 2010
Yuranga Weerakkody   +2 more
openaire   +2 more sources

The Association between Fetal Renal Artery Doppler Flow with Hourly Urine Output and Amniotic Fluid Volume of Fetuses with a Gestational Age of 30 to 34 Weeks [PDF]

open access: yesIranian Journal of Neonatology
Background: The present study investigated the association between fetal renal artery Doppler flow, hourly urine output, and amniotic fluid volume in fetuses with a gestational age of 30 to 34 weeks in normal pregnancies.
Neda Nikpour   +4 more
doaj   +1 more source

Fetal cerebral-umbilical Doppler ratio in prediction of fetal distress in patients with preeclampsia [PDF]

open access: yesVojnosanitetski Pregled, 2010
Bacground/Aim. The use of color Doppler ultrasonography provides noninvasive observation, confirmation and quantification of pathophysiological processes in fetoplacental circulation in pregnant patients.
Jurišić Aleksandar   +5 more
doaj   +1 more source

Blood flow-induced Notch activation and endothelial migration enable vascular remodeling in zebrafish embryos. [PDF]

open access: yes, 2018
Arteries and veins are formed independently by different types of endothelial cells (ECs). In vascular remodeling, arteries and veins become connected and some arteries become veins. It is unclear how ECs in transforming vessels change their type and how
Ablooglu, Ararat J   +6 more
core   +3 more sources

Trophoblast lineage-specific differentiation and associated alterations in preeclampsia and fetal growth restriction. [PDF]

open access: yes, 2020
The human placenta is a poorly-understood organ, but one that is critical for proper development and growth of the fetus in-utero. The epithelial cell type that contributes to primary placental functions is called "trophoblast," including two main ...
Farah, Omar   +3 more
core   +2 more sources

Development of clinical sign-based scoring system for assessment of omphalitis in neonatal calves [PDF]

open access: yes, 2018
Omphalitis contributes significantly to morbidity and mortality in neonatal calves. Diagnosis of omphalitis is based on the local signs of inflammation—pain, swelling, local heat and purulent discharge. An abattoir trial identified an optimal, sign-based,
Steerforth, D, Van Winden, S C L
core   +2 more sources

ALK1 controls hepatic vessel formation, angiodiversity, and angiocrine functions in hereditary hemorrhagic telangiectasia of the liver

open access: yesHepatology, EarlyView., 2022
Hepatic endothelial Alk1 signaling protects from development of vascular malformations while maintaining organ‐specific endothelial differentiation and angiocrine portmanteau of the names Wingless and Int‐1 signaling. Abstract Background and Aims In hereditary hemorrhagic telangiectasia (HHT), severe liver vascular malformations are associated with ...
Christian David Schmid   +20 more
wiley   +1 more source

Umbilical artery thrombosis

open access: yesMedicine, 2019
Abstract Rationale: The umbilical cord is the way to exchange gas, supply nutrients, excrete metabolized. Thrombosis of the umbilical cord leads to fetal hypoxia, which jeopardizes fetal health and can cause fetal death. Umbilical vessel thrombosis, which is rarely reported, is difficult to detect prenatally.
Li Huanxi   +4 more
openaire   +3 more sources

Isolation of equine endothelial cells and life cell angiogenesis assay [PDF]

open access: yes, 2014
Arterial or venous thromboses are frequent clinical complications with the risk of fatal progression. Recent studies suggest the disruption of angiogenesis in the course of thrombus resolution as the underlying pathomechanism.
Dietze, Kathrin   +5 more
core   +1 more source

Genetic predisposition to porto‐sinusoidal vascular disorder: A functional genomic‐based, multigenerational family study

open access: yesHepatology, EarlyView., 2022
A deleterious variant of FCHSD1 results in mTOR pathway overactivation and may cause porto‐sinusoidal vascular disorder (PSVD). The pedigree of the family demonstrated an autosomal dominant disease with variable expressivity. Whole‐genome sequencing and Sanger sequencing both validated the existence of the FCHSD1 variant and the heterozygosity of c ...
Jingxuan Shan   +19 more
wiley   +1 more source

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