Related Experiment Video
Updated: Dec 26, 2025

11:50
A Standardized Pipeline for Examining Human Cerebellar Grey Matter Morphometry using Structural Magnetic Resonance Imaging
Published on: February 4, 2022
4.4K
Correction to: Atrial myxoma with cerebellar signs: a case report
Suraj Shrestha1, Akash Raut2, Amar Jayswal1
1Maharajgunj Medical Campus, Maharajgunj, Kathmandu, Nepal.
Journal of Medical Case Reports
|March 19, 2020
Abstract:
In the publication of this article [1], there is an error in the name of one of the contributing authors.
Related Concept Videos
Aneurysm II: Clinical Manifestations and Diagnostic Studies
149
Thoracic, aortic arch and abdominal aneurysms are significant vascular conditions that can present with various clinical manifestations and lead to serious complications. Understanding these manifestations and the appropriate diagnostic studies is essential for effective management and treatment.Thoracic Aortic AneurysmsThoracic aortic aneurysms often remain asymptomatic until they reach a size that impinges on adjacent structures. They typically cause deep, diffuse chest pain that radiates to...
149
Mitral Stenosis II: Clinical features and Diagnostic Tests
154
Mitral stenosis is a heart condition in which the mitral valve, which allows blood to flow from the left atrium to the left ventricle, becomes narrowed or stenotic. This narrowing hinders blood flow and leads to clinical symptoms requiring specific medical evaluations and management strategies. The following overview outlines the clinical symptoms, assessments, diagnostic findings, prevention methods, and treatments for mitral stenosis.Clinical ManifestationsDyspnea (shortness of breath): This...
154
Cardiomyopathy III: Hypertrophic Cardiomyopathy
289
Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
289

