Results 51 to 60 of about 108,295 (312)

Acute onset of refractory hypoxemia: A rare hemodynamic cause of dyspnea

open access: yesIndian Journal of Respiratory Care, 2019
Platypnea-orthodeoxia syndrome (POS) is a rare condition of positional dyspnea with hypoxemia that can pose a diagnostic challenge to clinicians. We report two cases of POS with different pathophysiologic triggers and similar clinical features.
Tommaso Valobra   +2 more
doaj   +1 more source

Circulating Biomarkers and Cardiac Structure and Function in Rheumatoid Arthritis

open access: yesFrontiers in Cardiovascular Medicine, 2021
Background: Rheumatoid arthritis (RA) increases the risk for abnormalities of the cardiac structure and function, which may lead to heart failure (HF). Studying the association between circulating biomarkers and echocardiographic parameters is important ...
Masatake Kobayashi   +19 more
doaj   +1 more source

Understanding by general providers of the echocardiogram report

open access: yes, 2019
Echocardiograms are the second most frequently utilized cardiac test after electrocardiograms and are most commonly ordered by noncardiology providers. Echocardiogram reports are designed to communicate a comprehensive interpretation of cardiac function;
Tiwana, Jasleen   +9 more
core   +1 more source

Electrocardiogram and echocardiogram patterns among ischemic stroke patients during COVID-19 pandemic [PDF]

open access: yes, 2023
Objectives. Diabetic Ischemic strokes are mostly thromboembolic mainly originating from cardiac diseases. We aimed to assess electrocardiogram and echocardiogram abnormalities in patients with ischemic stroke during the COVID-19 pandemic.
Saeideh Aghayari Sheikh Neshin   +5 more
core   +1 more source

35 Individuals With HUWE1‐Related Neurodevelopmental Disorder and Suggested Clinical Evaluations

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT HUWE1 (HECT, UBA, and WWE Domain Containing E3 Ubiquitin Protein Ligase1, OMIM 300697), located at Xp11.22, encodes a ubiquitin ligase that is highly conserved across species. Genetic variants in HUWE1 described in multiple independent studies cause X‐linked intellectual disability, including in the patients identified by Juberg, Marsidi, and ...
Mindy H. Li   +25 more
wiley   +1 more source

Case Report: Myocardial dissection caused by ruptured sinus of Valsalva aneurysm in association with a bicuspid aortic valve

open access: yesFrontiers in Cardiovascular Medicine, 2023
In this report, we present a case of left-right sinus fusion in a Ruptured sinus of Valsalva aneurysm (RSVA) that perforated into the myocardium, giving rise to myocardial dissection.
Xinyan Zhou   +8 more
doaj   +1 more source

Cardiac Motions Classification on Sequential PSAX Echocardiogram

open access: yes, 2018
Cardiac wall motions classification on 2-dimensional (2D) echocardiographic images is an important issue for quantitative diagnosiing of heart disease. Unfortunately, the bad quality of echocardiogram cause computationally classification on cardiac wall ...
Riyanto Sigit   +7 more
core   +2 more sources

The Critical Role of Fractionated Urine Glycosaminoglycans in the Evaluation of Mucopolysaccharidosis Type II in Four Unrelated Families

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Since 2015, Ann and Robert H. Lurie Children's Hospital has performed diagnostic testing for infants who screen positive for mucopolysaccharidosis type II (MPS II) on the Illinois newborn screen. Preliminary diagnostic testing includes measurement of plasma iduronate‐2‐sulfatase enzyme activity and urinary glycosaminoglycan analysis, followed ...
Carly A. Rasmussen   +5 more
wiley   +1 more source

Echocardiogram parameters 15 days after I/R.

open access: yes, 2015
SF: Shortening fraction; EF: Ejection fraction; LV: Left ventricle; AW: Anterior wall; CO: Cardiac output. Echocardiogram parameters were calculated according to Eqs 1–3 (see text). Data expressed as mean ± SEM.*P < 0.05 with respect to the corresponding
Paulo André Silva (811091)   +11 more
core   +1 more source

Long‐Term Follow Up of Two Patients With Variants in the Cluster 1031‐1159 of TRRAP Gene: Expanding the Phenotype of Developmental Delay With or Without Dysmorphic Facies and Autism

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The transformation/transcription domain‐associated protein (TRRAP) gene encodes a large multidomain protein, a member of the phosphatidylinositol 3‐kinase‐related kinase (PIKK) family. TRRAP is a component of the histone acetyltransferase (HAT) complex, and it plays an important role in gene transcription, DNA repair, and cell‐cycle regulation.
Roseli Maria Zechi‐Ceide   +10 more
wiley   +1 more source

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