Results 31 to 40 of about 316,277 (255)

The right coronary artery originating from the distal circumflex artery [PDF]

open access: yesĶazaķstannyṇ Klinikalyķ Medicinasy, 2019
We report a case of anomalous origin of the right coronary artery in a 58-year-old male patient. The patient had a single coronary ostium originating from the left sinus valsalva.
Songül Cuglan, Bilal Cuglan
doaj   +1 more source

Unilateral absence of the left pulmonary artery with patent ductus arteriosus and interrupted inferior vena cava

open access: yesTürk Kardiyoloji Derneği Arşivi, 2014
Unilateral absence of the pulmonary artery and interrupted inferior vena cava are rare congenital disorders. The clinical presentation is variable, and many patients can be asymptomatic for many years and even throughout their lives.
Burçak Kılıçkıran Avcı   +3 more
doaj   +1 more source

Combination between Dunbar Syndrome and May–Thurner syndrome: A rare case Report

open access: yesJournal of Medical Ultrasound, 2023
Dunbar syndrome (DS) and May–Thurner syndrome (MTS) are part of a group of rare vascular disorders known as “vascular compression syndromes.” Dunbar's syndrome is caused by the median arcuate ligament of diaphragm, which, due to an abnormal course ...
Renato Farina   +3 more
doaj   +1 more source

Alterations in Electrolyte and Renal Profile in Chronic Kidney Disease Patients with Coexisting Cardiovascular Complications: A Cross-sectional Study [PDF]

open access: yesJournal of Clinical and Diagnostic Research
Introduction: Chronic Kidney Disease (CKD) is often complicated by coexisting Cardiovascular Disease (CVD), which increases morbidity and influences biochemical markers.
Apoorva Gupta   +3 more
doaj   +1 more source

Cardiovascular Abnormalities in Hyperthyroidism

open access: yesThe American Journal of Medicine, 2006
Anthonisen et al in 1987 continues to be the landmark study. 3 The inclusion criteria required COPD with a FEV1 70% and FEV1/forced vital capacity 70%. It must be kept in mind that patients in the former study had a mean FEV1 of only 33.9% predicted.
Çakır, Mehtap, Can, İlknur
openaire   +3 more sources

Cardiovascular abnormalities in osteogenesis imperfecta

open access: yesAmerican Heart Journal, 1983
To investigate the prevalence of cardiac abnormalities in osteogenesis imperfecta we performed a clinical and echocardiographic study on 20 patients. One patient had aortic regurgitation, 13 had soft late apical systolic murmurs (without significant mitral regurgitation), and seven had systemic hypertension.
White, N, Winearls, C, Smith, R
openaire   +2 more sources

Risk of sudden cardiac death and preventive measures in athletes

open access: yesInternational Journal of the Cardiovascular Academy, 2022
Arrhythmias, which are fatal in some patients, can be triggered by sports in vulnerable people. It is estimated that 1:40,000–1:250,000 athletes will suffer a sudden cardiac death (SCD).
Adel Khalifa Sultan Hamad
doaj   +1 more source

Cumulative Lifetime Burden of Cardiovascular Disease From Early Exposure to Air Pollution

open access: yesJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2020
The disease burden associated with air pollution continues to grow. The World Health Organization (WHO) estimates ≈7 million people worldwide die yearly from exposure to polluted air, half of which—3.3 million—are attributable to cardiovascular disease ...
Juyong Brian Kim   +11 more
doaj   +1 more source

Clinical and Genetic Characteristics of Familial Hypercholesterolemia at Sultan Qaboos University Hospital in Oman

open access: yesOman Medical Journal, 2020
Objectives: We sought to describe the clinical and genetic characteristics of patients with familial hypercholesterolemia (FH) that presented to the lipid clinic at Sultan Qaboos University Hospital, Muscat, Oman.
Khalid Al-Waili   +9 more
doaj   +1 more source

What endocrinologists can do to prevent cardiovascular complications in adults with Prader-Willi syndrome: Lessons from a case series

open access: yesFrontiers in Endocrinology, 2023
ContextPrader-Willi syndrome (PWS) is a complex rare genetic syndrome. Mortality in patients with PWS is 3% per year. In nearly half of the patients, the cause of death is of cardiopulmonary origin.
Karlijn Pellikaan   +17 more
doaj   +1 more source

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