Results 151 to 160 of about 290,434 (263)

Transition From Pulmonary to Gastrointestinal Hemorrhage: A Rare Case of Hematemesis in an Adolescent With Chronic Pulmonary Hypertension and Valvular Regurgitation

open access: yesClinical Case Reports, Volume 14, Issue 9, September 2026.
Graphical abstract summarizing hematemesis associated with pulmonary hypertension and valvular regurgitation. Negative gastrointestinal evaluation suggested a cardiopulmonary source. Conservative management resolved the hematemesis. ABSTRACT Pulmonary hypertension is a chronic cardiopulmonary disease with increased pulmonary arterial pressure and right‐
Bilal Ashraf   +6 more
wiley   +1 more source

Thrombus‐Induced Prosthetic Valve Dysfunction Demonstrating Hypo‐Attenuated Leaflet Thickening: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Hypo‐attenuated leaflet thickening (HALT) is an important and potentially underrecognized cause of late bioprosthetic valve dysfunction after surgical AVR. Multimodal imaging, including echocardiography and electrocardiogram‐gated computed tomography, is essential for diagnosis, and timely surgical or medical intervention can effectively ...
Takanori Kono   +4 more
wiley   +1 more source

miR‐138‐5p Inhibits Aortic Valve Interstitial by Targeting SLC39A14 and Activating Nrf2 Signaling

open access: yesJournal of Biochemical and Molecular Toxicology, Volume 40, Issue 9, September 2026.
Nrf2 Pathway Inhibition Attenuates miR‐138‐5p's Anti‐Calcification Effects in OM‐Induced hAVICs. A. ALP staining for ALP activity assessment in NC‐mimic, miR‐mimic, and miR‐mimic + ML385 groups. B. Alizarin Red staining for osteogenesis and calcium nIn osteogenic medium‐induced human aortic valve interstitial cells (hAVICs), miR‐138‐5p targets SLC39A14
Fei Yan   +9 more
wiley   +1 more source

Predictive value of cardiothoracic ratio as a marker of severity of aortic regurgitation and mitral regurgitation

open access: yes, 2007
Objective: In this study we compared cardiothoracic ratio on chest radiography and left ventricular dimensions from echocardiography in patients with left heart valvular regurgitation.
Ouztunc, Funda   +4 more
core  

Asymptomatic Giant Right Ventricular Myxoma in an Adolescent: A Rare Case Report With Favorable Surgical Outcome

open access: yesJournal of Clinical Ultrasound, Volume 54, Issue 7, Page 1790-1794, September 2026.
We report a 13‐year‐old female with a giant right ventricular myxoma extending to the pulmonary trunk. The tumor was diagnosed by multimodal imaging and completely resected, with favorable short‐term outcomes. ABSTRACT Right ventricular (RV) myxomas account for < 5% of cardiac myxomas and are often asymptomatic, easily overlooked.
Aizezi Maihemu   +3 more
wiley   +1 more source

Severe aortic regurgitation revealing Takayasu arteritis: a case report. [PDF]

open access: yesEur Heart J Case Rep
Dommane FE   +3 more
europepmc   +1 more source

Acute Rheumatic Fever Without Pharyngitis: A Case Report

open access: yesJournal of General and Family Medicine, Volume 27, Issue 5, September 2026.
ABSTRACT An 18‐year‐old man presented with fatigue and polyarthralgia refractory to nonsteroidal anti‐inflammatory drugs (NSAIDs). He had no history of sore throat or other upper respiratory symptoms. Reactive arthritis was initially suspected. However, persistent symptoms, fever, polyarthritis, a cardiac murmur, atrioventricular block, and an elevated
Hiroki Suzuyama   +7 more
wiley   +1 more source

Platypnea-Orthodeoxia After TAVI for Severe Aortic Regurgitation: A Breathless Surprise. [PDF]

open access: yesJACC Case Rep
Kopp S   +5 more
europepmc   +1 more source

Unmasking Mucopolysaccharidosis Type I in a Patient With Wolf–Hirschhorn Syndrome: Diagnostic Overshadowing

open access: yesJIMD Reports, Volume 67, Issue 5, September 2026.
ABSTRACT Mucopolysaccharidosis Type I (MPS I) is a rare lysosomal storage disorder caused by α‐l‐iduronidase deficiency, leading to glycosaminoglycan accumulation and multisystem involvement. Wolf–Hirschhorn Syndrome (WHS) is a chromosomal disorder characterized by growth delay, dysmorphism, and developmental impairment.
Karla Cifuentes‐Uribe   +4 more
wiley   +1 more source

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