Medium-chain acyl-CoA dehydrogenase deficiency (MCADD) is the most common inherited
mitochondrial metabolic disease of fatty acid β-oxidation, especially in newborns. MCADD is …

Background Autoimmune thyroid disease (AITD) can cause enormous health burdens;
however, trustworthy biomarkers in identifying the onset and progression of AITD are limited …

Introduction: Galactosemia (GAL) is a genetic disorder that results in disturbances in
galactose metabolism and can lead to life-threatening complications. However, the …

The most prevalent comorbidity among cystic fibrosis (CF) patients is cystic fibrosis-related
diabetes (CFRD). CFRD has been linked to one of the worse clinical outcomes and a higher …

Herbal products have been very popular in Pakistan for their curative significance against
various disorders. Demaghi (DEMG) is a widely used herbal product claimed to own natural …

Very long-chain acylcarnitine dehydrogenase deficiency (VLCADD) is a rare inherited
metabolic disorder associated with fatty acid β-oxidation and characterized by genetic …

The clinicopathological characteristics and outcomes of patients infected with hepatitis B
virus (HBV) differ between genotypes B and C. However, the potential metabolic …

Hyperthyroidism is the most common feline endocrinopathy. In hyperthyroid humans,
untargeted metabolomic analysis identified persistent metabolic derangements despite …

Background/Objectives: Understanding the metabolic responses to different macronutrients
is crucial for assessing their impacts on health. This study aims to investigate the …

Background: Liraglutide, a long-acting glucagon-like peptide-1 receptor agonist (GLP1RA),
is a well-established anti-diabetic drug, has also been approved for the treatment of obesity …