Results 231 to 240 of about 182,011 (335)

What's Your Diagnosis? A Case of Extreme Thrombocytosis in a Dog

open access: yes
Veterinary Clinical Pathology, EarlyView.
Stephanie F. Anderson   +5 more
wiley   +1 more source

Mitochondrial Dysfunction in Propionic Acidemia: A Case‐Report and Review of the Literature

open access: yesJIMD Reports, Volume 67, Issue 2, March 2026.
ABSTRACT Propionic acidemia is an inborn error of metabolism involving an enzymatic defect of propionyl‐CoA carboxylase that results in the build‐up of toxic metabolites which can induce metabolic decompensation. Secondary mitochondrial dysfunction in propionic acidemia has been commonly recognized; however, its clinical presentation and management are
Brandon K. Walther   +5 more
wiley   +1 more source

Strategies to Identify Echocardiogram Complexity to Support Learning Echocardiogram Interpretation

open access: yesCanadian Journal of Cardiology
Thomas C. Raissi   +9 more
openaire   +2 more sources

International Contrast Ultrasound Society Safety Round Table

open access: yesJournal of Ultrasound in Medicine, Volume 45, Issue 3, Page 473-485, March 2026.
The international Contract Ultrasound Society (ICUS) held a round table discussion on the safety of ultrasound contrast agents for cardiology, radiology, and pediatrics on September 4, 2024. The panel included international experts on ultrasound contrast.
Richard G. Barr   +5 more
wiley   +1 more source

Severe Aortic Regurgitation Due to Quadricuspid Aortic Valve. [PDF]

open access: yesJACC Case Rep
Elalfy A   +4 more
europepmc   +1 more source

Comparison of 3D Echocardiogram-Derived 3D Printed Valve Models to Molded Models for Simulated Repair of Pediatric Atrioventricular Valves

open access: yesPediatric Cardiology, 2018
Adam B. Scanlan   +13 more
semanticscholar   +1 more source

Association between RoPE score and PFO grading on bubble echocardiography in cryptogenic stroke patients: a retrospective cohort study. [PDF]

open access: yesFront Stroke
Rahman S   +8 more
europepmc   +1 more source

Clinical, genetic, and familial features of POT1 tumor predisposition syndrome

open access: yesCancer, Volume 132, Issue 4, 15 February 2026.
Abstract Background Protection of telomere 1 (POT1) tumor predisposition syndrome (POT1‐TPD) is a hereditary leukemia syndrome that is identified in ∼5% of patients with chronic lymphocytic leukemia (CLL) and is characterized by a predisposition to other cancers, including gliomas, melanomas, and angiosarcomas.
Courtney D. DiNardo   +13 more
wiley   +1 more source

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