Results 31 to 40 of about 25,743 (222)

Dysphagia Secondary to Esophageal Compression in a Patient with Decompensated Heart Failure [PDF]

open access: yesThe Korean Journal of Helicobacter and Upper Gastrointestinal Research, 2022
Cardiogenic dysphagia is a rare type of esophageal dysphagia caused by external compression of the esophagus by an enlarged left atrium. Long-term comparisons between the degree of cardiogenic dysphagia and heart failure have not been reported due to its
Jintae Park   +4 more
doaj   +1 more source

An unusual cause of cardiomegaly [PDF]

open access: yesEuropean Heart Journal, 2008
A 38-year-old male patient was referred to our institution to study the origin of global cardiomegaly observed in a chest radiograph ( Panel A ). No remarkable data were reported in his medical record excepting hip fracture at the age of 3 after a road traffic accident, which required surgery. He was asymptomatic and …
Esther, Pérez David   +2 more
openaire   +2 more sources

Properties of Myocardium in Cardiomegaly [PDF]

open access: yesCirculation Research, 1963
The adult rat's ventricular myocardium is able to increase its mass markedly while maintaining its unit quality. It does so by maintaining constant the design of the sarcomeres: an increase in length is accomplished by the addition of sarcomeres in series; an increase in tension production is accomplished by the addition of more cross-sectional area of
A F, GRIMM, R, KUBOTA, W V, WHITEHORN
openaire   +2 more sources

Familial Idiopathic Cardiomegaly [PDF]

open access: yesCirculation, 1961
Two young adult sisters are described with clinical and pathologic findings of myocardial disease. These cases along with a suggestive family history are presented as examples of familial idiopathic cardiomegaly. Pathologic findings are compared and contrasted with those in the literature, and etiologic concepts are discussed.
W H, SCHRADER   +3 more
openaire   +2 more sources

Non-Cardiac Cause of Death in Selected Group Children with Cardiac Pathology: A Retrospective Single Institute Study

open access: yesChildren, 2022
Background: Pediatricians and pediatric surgeons often face children with cardiomegaly and dilatative or hypertrophic cardiomyopathies presenting with or without symptoms.
Stefana Maria Moisa   +6 more
doaj   +1 more source

Dead Bodybuilders Speaking from the Heart: An Analysis of Autopsy Reports of Bodybuilders That Died Prematurely

open access: yesJournal of Functional Morphology and Kinesiology, 2022
This study analyzed publicly available autopsy reports of male bodybuilders under the age of 50 who reportedly died from cardiovascular-related events. A general Google search with the terms “dead bodybuilders” was performed on 10 February 2022.
Guillermo Escalante   +4 more
doaj   +1 more source

Syphilitic heart - a case report

open access: yesNational Journal of Clinical Anatomy, 2013
Heart and its great vessels are involved in tertiary syphilis in the form of syphilitic aortitis often 20 years or more after primary infection is contracted.
K C Jyothi   +3 more
doaj   +1 more source

An Observational Data Analytical Research on Pediatric Cardiomegaly as a Predictor of Structural or Functional Heart Diseases: Chest X-ray versus Echocardiography Comparison and Contemplation

open access: yesJournal of the Indian Academy of Echocardiography & Cardiovascular Imaging, 2022
Background: Chest X-ray (CXR) is a routine, noninvasive test advised in a plethora of pediatric non-cardiac conditions such as bronchopneumonia, respiratory distress, failure to thrive, suspected tuberculosis, and for preoperative anesthesia clearance ...
Munesh Tomar   +3 more
doaj   +1 more source

Vertebral Heart Score and Vertebral Left Atrial Size as Radiographic Measurements for Cardiac Size in Dogs—A Literature Review

open access: yesAnimals
Radiology plays an important role in veterinary cardiology, along with other methods, such as electrocardiography, echocardiography, and biomarkers, in the diagnosis of cardiac diseases.
Radu Andrei Baisan, Vasile Vulpe
doaj   +1 more source

Response of an Infant With Presumed Multiple Acyl‐CoA Dehydrogenase Deficiency (MADD) to Ketone Supplementation

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Multiple Acyl‐CoA Dehydrogenase Deficiency (MADD) is an autosomal recessive inborn error of metabolism caused by biallelic pathogenic variants in one of three known genes: ETFA, ETFB, and ETFDH. It can cause multisystem dysfunction, including cardiomyopathy in severe cases.
Yutaka Furuta   +17 more
wiley   +1 more source

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