Results 91 to 100 of about 67,540 (236)

Transplant Renal Artery Stenosis [PDF]

open access: yesKidney International Reports, 2020
David P. Baird   +3 more
openaire   +2 more sources

Impact of Partial Echo on 4D Flow MRI: The Insight From Synthetic MRI

open access: yesMagnetic Resonance in Medicine, EarlyView.
ABSTRACT Purpose The aim of this study is to investigate the impact of the partial echo on 4D flow MRI sequences thanks to in silico coupled MRI‐CFD (computational fluid dynamics) simulations. Methods Two sequences are studied: one with a full echo (FE) and another using partial echo (PE) with an echo symmetry fraction of 0.75.
Morgane Garreau   +6 more
wiley   +1 more source

Respiratory Motion‐Corrected Model‐Based 3D Water‐Fat MRA of the Thorax at 0.55 T

open access: yesMagnetic Resonance in Medicine, EarlyView.
ABSTRACT Purpose The goal of this study was to develop a 5‐min 3D MRA acquisition at 0.55 T with predictable scan time, 100% data efficiency, and robust water‐fat separation. Methods For full data efficiency, the proposed method combined self‐gating with retrospective motion correction while ensuring a predictable 5‐min scan time.
Robert Stoll   +5 more
wiley   +1 more source

Renal Artery Stenosis

open access: yesGomal Journal of Medical Sciences, 2005
Habib-ullah Khan   +3 more
doaj   +1 more source

Current Status of Kidney Xenotransplantation in Basic Research

open access: yesOrgan Medicine, EarlyView.
Kidney xenotransplantation is a potential solution to the organ shortage for end‐stage kidney disease. This review systematically elaborates on the application advances of donor pig gene editing technologies, the molecular mechanisms and regulatory strategies of xenogeneic immune rejection, and the optimization approaches of immune compatibility ...
Yu Luo, Bingzhuo Liu, Weijie Lai
wiley   +1 more source

Yield of Whole Genome Sequencing for Pathogenic Single Nucleotide Variants in Congenital Heart Disease: A Systematic Review and Meta‐Analysis

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objective This systematic review and meta‐analysis aimed to assess the diagnostic yield of pathogenic or likely pathogenic (P/LP) single nucleotide variants (SNVs) using whole genome sequencing (WGS) in congenital heart disease (CHD). Methods A systematic search of three databases (2000–2024) was conducted, and two reviewers independently ...
Hiba J. Mustafa   +7 more
wiley   +1 more source

Diagnosis and treatment of pediatric arterial stenosis associated with neurofibromatosis type 1

open access: yesBMC Pediatrics
Background Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting multiple systems. However, arterial stenosis is a rare manifestation in patients with NF1.
Haichong Li   +5 more
doaj   +1 more source

The Expanding Role of Gene Sequencing in Shaping Fetal Therapies: Clinical and Ethical Considerations

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT In utero interventions are transformative in addressing genetic and anatomic conditions during fetal development. Next generation sequencing enables early genetic testing, playing a pivotal role in prenatal decision‐making by supporting risk stratification, precise and timely diagnosis, which directly informs eligibility for fetal surgical and
Matthew A. Shear   +7 more
wiley   +1 more source

Renal artery branch stenosis induced hypertension in children: a case series

open access: yesBMC Pediatrics
Purpose Renal artery branch stenosis induced hypertension (HTN) in children is rare and facing a great challenge in diagnosis and treatment. This study aimed to summarize the clinical features and experience in diagnosis and treatment of these children ...
Hongwei Zhang   +6 more
doaj   +1 more source

NONO‐Related Syndromic X‐Linked Developmental Disability 34: Further Clinical and Molecular Delineation in a Prenatal Cohort

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objective To characterize the prenatal sonographic features across different trimesters and genomic spectrum of NONO‐related X‐linked intellectual developmental disorder. Method We analyzed two fetuses presenting with corpus callosum agenesis and rare cardiac anomalies using genome sequencing and exome sequencing.
Yilin Zhao   +13 more
wiley   +1 more source

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