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February 22, 2025


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Volume 6

effect of resistance exercises with Salvia officinalis supplementation on the response of some bio-hormones in overweight male students

1.1. Background: The aim of this study was the effect of resistance exercises with sage supplementation on the response of some bio-hormones in overweight male students.

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Duchenne Muscular Dystrophy Improved Clinically by Homeopathy: A Case Report

Muscular dystrophy is a group of multiple inherited diseases that damage muscles with time and causes a partial or complete loss of movement. It happens due to the lack of protein dystrophin, which is important for normal muscle functioning. The most common type of muscular dystrophy is Duchenne muscular dystrophy which appears at an early age and progresses with time. Frequent falls, difficulty rising from a sitting or lying position, difficulty running and improper gait, large calf muscles, and concentration problems are all common symptoms of the disease. Diagnosis is usually made on presenting complaints and elevation of CPK-3 in blood.

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Prevalence of Cns Tumors and Histological Recognition in the Operated Patients: 10 Years Experience

1.1. Background: Tumors of the central nervous system consist of a heterogeneous group of neoplasms of great histological diversity. Despite the increasing prevalence of these tumors in developing countries, some places like Yemen do not have representative studies showing the true impact of these tumors on our population.

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Asymptomatic right atrial lipoma in a 42-year-old patient:A case report

Lipoma, a common soft tissue tumor composed of mature adipose tissues, can occur in any part of the body with fat. Accounting for 8.4% of primary heart tumors [1], the lipoma in the heart is rare, and the most common sites are the right atrium, left ventricle, and pericardium [2,3]. Most patients with cardiac lipomas have no symptoms, and some may experience palpitations, syncope, or even cardiac arrest [4, 5].

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Clinical and Genetic Analysis of Multi-System Pseudohypoaldosteronism Type 1 Caused by a Novel Splice Site Mutation of the Beta Subunit Gene of Epithelial Sodium Channel (Enac)

1.1. Background: This article aims to provide a comprehensive review of the clinical features and genetics basis of multi-system pseudohypoaldosteronism type 1 caused by SCNN1B gene mutations.

Clinical and Genetic Analysis of Multi-System Pseudohypoaldosteronism Type 1 Caused by a Novel Splice Site Mutation of the Beta Subunit Gene of Epithelial Sodium Channel (Enac) Read More »

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