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Mitochondrial Encephalomyopathy With Lactic Acidosis and Stroke-Like Episodes (MELAS): An Overview
Mitochondrial Encephalomyopathy With Lactic Acidosis and Stroke-Like Episodes (MELAS) is a rare genetic disease impairing the function of mitochondria.
Human Mitochondrial Genetics - Mitochondrial Genes
Human mitochondrial genetics is a branch of biology that deals with the study of mitochondrial genes, for more information continue reading.
Mitochondrial Damage and Kidney Disease - Unveiling the Link
Mitochondrial damage exacerbates kidney disease progression, highlighting the intricate interplay between cellular health and renal function.
Mitochondrial Disorders - Inheritance, Implications, and Investigations
Mitochondrial diseases encompass a genetically and clinically diverse group of diseases due to defects in mitochondria. Read below to learn more.
Mitochondrial Disorders and Hepatic Dysfunction in Children
Mitochondrial disorders are complex disorders seen commonly in children and involving the liver. It is very variable, and symptoms depend on severity.
Smart Insulin Patches: Technical Breakthrough in Diabetes
Smart insulin patches are revolutionary insulin administrators that change the experience of diabetes care. Read more»Probiotics in Nonalcoholic Fatty Liver Disease (NAFLD) - Prevention and Management
The gut microbiome is closely linked to the development of NAFLD. In NAFLD cases, probiotic therapy regulates liver function, insulin, and lipid levels. Read more»Effective Strategies for Managing Anterior Epistaxis in Older Adults
Epistaxis or nosebleeds can be prevented through humidifiers, Aspirin, decongestants, and avoiding nose trauma. Read more»