Volume 10
Paget-Schroeter Syndrome Is Still Uncommon or Increasingly Common!
1. Abstract
Upper extremity deep venous thrombosis (UEDVT) is a condition characterised by thrombosis in the veins of the upper limb.
No Significant Liver Disease or True Immune-tolerant HBeAg Positive Chronic Hepatitis B with Normal Serum ALT Levels
1.1. Background
Hepatitis B e antigen (HBeAg)-positive Chronic hepatitis B (CHB) patients with normal alanine aminotransaminase (ALT) were usually considered to be in the immune-tolerant phase. However, it has been suggested that the current upper limit of normal for ALT should be lowered.
Total Number of Polyps are Associated with an Increased Risk of Recurrent Adenomatous Polyps
1. Abstract
1.1. Background
Current guidelines on interval between surveillance colonoscopy is limited by insufficient understanding about the rate of polyp re-growth.
Spontaneous Pediatric Colon Perforation: A Rare Case Report
1. Abstract
Idiopathic colon perforation is a rare condition in children, more commonly observed at the extremes of age. Frequent sites include the splenic flexure.
A Link Between Type I Diabetes Mellitus and Microscopic Colitis: A State-Wide Retrospective Analysis
1. Abstract
Type 1 diabetes mellitus (T1DM) and microscopic colitis (MC) share autoimmune mechanisms. A retrospective study at UAMS found 22 MC cases among 2,978 T1DM patients, predominantly in Caucasian females aged 60-80.
Postbiotic’s Role in the Gut-Brain Axis During Neonatal Age
1. Abstract
1.1. Background
Postbiotics, biologically active compounds derived from probiotics, are increasingly recognized for their potential influence on the gut-brain axis (GBA), particularly during the neonatal period.
Absence of Organs Dental Trigger Gastrointestinal Disorders
1.Introduction
Oral health influences the general well-being of our body and, in many cases, losing teeth is not is only a problem for chew, but that
can bring with him complications in he system digestive.
Analysis of Genetic Variants and Methylation Alterations in Lynch Syndrome Associated Cancers
1. Abstract
Lynch syndrome (LS) is a hereditary cancer syndrome caused by mutations in DNA mismatch repair (MMR) genes, leading to microsatellite instability (MSI) and increased cancer risk.
