News Update on Neuroblastoma : Jan 2022
Molecular Biology of Neuroblastoma PURPOSE AND RESULTS: Neuroblastoma, the most common solid extracranial neoplasm in children, is remarkable for its clinical heterogeneity. Complex patterns of...
Mechanism(s) of Membrane Permeability Transition in Liver Mitochondria of Lamprey, Lampetra fluviatilis L. during Pre-spawning Starvation
The opening of the mitochondrial permeability transition (MPT) pore in its low conductance state occurs in the hepatocytes of the Baltic lamprey (Lampetra fluviatilis L.)...
A Review of the Recent Advances in the Surgical Treatment of Longstanding Facial Paralysis
Facial paralysis affects people of all ages and has far-reaching functional and psychological implications. Surgical therapy is the sole choice in some circumstances, and it...
A Study about Cystoscope: A Viable Alternative Tool for Choledochoscopy
To avoid difficulties caused by retained/recurrent stones, complete bile duct stone clearance is required following bile duct exploration. While there is no one optimum procedure,...
Role of Dexamethasone in Prevention of Pain Flares in Painful Bone Metastases after Radiotherapy
In oncology practise, metastatic bone disease is a common concern. Bone is a common location of metastasis in solid malignancies. After the liver and the...
Parental Educational Background and Socio Economic Status of ASD Children in Bangladesh: A Cross Sectional Study
Bangladesh is a developing country where the majority of the population lives in poverty. Autism is a major problem in our country today. Autism spectrum...
AhR-NQO1 Signaling in Hepatocytes Drives a Protective Response against Alcohol-induced NAD+ Depletion and Liver Damage
ALD (alcohol-related liver disease) is one of the most common types of liver disease worldwide. It's critical to gain a better knowledge of the molecular...
Determination of Breast Cancer in Women Under 40 Years Old at Yalgado Ouédraogo University Hospital, Burkina Faso
Introduction: Breast cancer management in Burkina Faso is still difficult due to late diagnosis. The therapy options are restricted, and complications are common, resulting in...
A Case Report with Literature-Based Analysis of Hereditary Angioedema Caused by C1-Esterase Inhibitor Deficiency
C1-esterase inhibitor deficiency causes hereditary angioedema (HAE), which is an autosomal-dominant illness caused by a mutation in the C1-inhibitor gene. It's a rare condition that's...
Determination of the Anti-diabetic Activity of Sphenostylis stenocarpa Seed Milk Extract in Alloxan-induced Diabetes Rats
Diabetes mellitus is a chronic metabolic disorder characterised by improper glucose, protein, and lipid metabolism. It's generally connected with glycosuria, or the discharge of too...