Search Results - "Mason, Stefanie"
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Significant Spirometric Transitions and Preserved Ratio Impaired Spirometry Among Ever Smokers
Published in Chest (01-03-2022)“…Emerging data from longitudinal studies suggest that preserved ratio impaired spirometry (PRISm), defined by proportionate reductions in FEV1 and FVC, is a…”
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Relationship between Emphysema Progression at CT and Mortality in Ever-Smokers: Results from the COPDGene and ECLIPSE Cohorts
Published in Radiology (01-04-2021)“…Background The relationship between emphysema progression and long-term outcomes is unclear. Purpose To determine the relationship between emphysema…”
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Preoperative Brain Injury in Transposition of the Great Arteries Is Associated With Oxygenation and Time to Surgery, Not Balloon Atrial Septostomy
Published in Circulation (New York, N.Y.) (10-02-2009)“…Preoperative brain injury is an increasingly recognized phenomenon in neonates with complex congenital heart disease. Recently, reports have been published…”
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Quantitative Interstitial Abnormality Progression and Outcomes in the Genetic Epidemiology of COPD and Pittsburgh Lung Screening Study Cohorts
Published in Chest (01-01-2023)“…The risk factors and clinical outcomes of quantitative interstitial abnormality progression over time have not been characterized. What are the associations of…”
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Distinguishing Smoking-Related Lung Disease Phenotypes Via Imaging and Molecular Features
Published in Chest (01-02-2021)“…Chronic tobacco smoke exposure results in a broad range of lung pathologies including emphysema, airway disease and parenchymal fibrosis as well as a multitude…”
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Semi-quantitative visual assessment of chest radiography is associated with clinical outcomes in critically ill patients
Published in Respiratory research (12-10-2019)“…Respiratory pathology is a major driver of mortality in the intensive care unit (ICU), even in the absence of a primary respiratory diagnosis. Prior work has…”
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Optical measurement of cerebral hemodynamics and oxygen metabolism in neonates with congenital heart defects
Published in Journal of Biomedical Optics (01-05-2010)“…We employ a hybrid diffuse correlation spectroscopy (DCS) and near-infrared spectroscopy (NIRS) monitor for neonates with congenital heart disease (n=33). The…”
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Cost-effectiveness microsimulation of catheter-directed thrombolysis in submassive pulmonary embolism using a right ventricular function model
Published in Journal of thrombosis and thrombolysis (01-05-2020)“…Approximately 30–50% of hemodynamically stable patients presenting with acute pulmonary embolism (PE) have evidence of right ventricular (RV) dysfunction…”
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Seizures as a Presenting Symptom of Acute Arterial Ischemic Stroke in Childhood
Published in The Journal of pediatrics (01-09-2011)“…Objectives To define the incidence of seizures as a presenting symptom of acute arterial ischemic stroke (AIS) in children and to determine whether younger…”
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Arterial spin labeling perfusion MRI in pediatric arterial ischemic stroke: Initial experiences
Published in Journal of magnetic resonance imaging (01-02-2009)“…Purpose To investigate the feasibility and utility of arterial spin labeling (ASL) perfusion MRI for characterizing alterations of cerebral blood flow (CBF) in…”
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O19: Integrated analyses of data from clinical trials of delandistrogene moxeparvovec gene therapy in DMD
Published in Genetics in Medicine Open (2023)Get full text
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The implication of coronary artery malformations and congenital heart disease on cardiomyopathy
Published in Progress in pediatric cardiology (01-12-2014)“…Abstract Coronary and congenital heart malformations contribute to and overlap with clinical cardiomyopathy. As cellular mechanisms and gene associations are…”
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Long‐term safety and functional outcomes of delandistrogene moxeparvovec gene therapy in patients with Duchenne muscular dystrophy: A phase 1/2a nonrandomized trial
Published in Muscle & nerve (01-01-2024)“…Introduction/Aims Delandistrogene moxeparvovec is indicated in the United States for the treatment of ambulatory pediatric patients aged 4 through 5 years with…”
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Practical Considerations for Delandistrogene Moxeparvovec Gene Therapy in Patients With Duchenne Muscular Dystrophy
Published in Pediatric neurology (01-04-2024)“…Delandistrogene moxeparvovec is a gene transfer therapy approved in the United States, United Arab Emirates, and Qatar for the treatment of ambulatory patients…”
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Delandistrogene Moxeparvovec Gene Therapy in Ambulatory Patients (Aged ≥4 to <8 Years) with Duchenne Muscular Dystrophy: 1‐Year Interim Results from Study SRP‐9001‐103 (ENDEAVOR)
Published in Annals of neurology (01-11-2023)“…Objective Delandistrogene moxeparvovec is approved in the USA for the treatment of ambulatory patients (4–5 years) with Duchenne muscular dystrophy. ENDEAVOR…”
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EMBARK, a Phase 3 Trial Evaluating Safety and Efficacy of Delandistrogene Moxeparvovec (SRP- 9001) in Duchenne Muscular Dystrophy (DMD): Study Design and Baseline Characteristics (P5-8.012)
Published in Neurology (25-04-2023)“…Abstract only…”
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One-year Data from ENDEAVOR, a Phase 1b Trial of Delandistrogene Moxeparvovec (SRP-9001) in Patients with Duchenne Muscular Dystrophy (DMD) (S48.003)
Published in Neurology (25-04-2023)“…Abstract only…”
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Integrated Analyses of Data from Clinical Trials of Delandistrogene Moxeparvovec (SRP-9001) in Duchenne Muscular Dystrophy (DMD) (S48.006)
Published in Neurology (25-04-2023)“…Abstract only…”
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Long-term Safety and Efficacy in Patients with DMD 4 Years Post-Treatment with Delandistrogene Moxeparvovec (SRP-9001) in a Phase 1/2a Study (P3-8.006)
Published in Neurology (25-04-2023)“…Abstract only…”
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