Recent studies shed light on promising treatments targeting HER2 mutations and the effectiveness of PD-L1 IHC assays in lung cancer, offering hope for more personalized and effective therapies.
Worried about fatty liver? Discover why MRI scans are a trustworthy tool for measuring liver fat, offering consistent results despite biological differences. This article breaks down the science and offers peace of mind.
Discover how a targeted teaching approach can significantly improve pregnant women's knowledge of toxoplasmosis. Learn about the unexpected link between awareness and anxiety, and what it means for maternal health in Northern Upper Egypt.
Explore the 150-year journey since Charcot's foundational lectures on multiple sclerosis, highlighting current research, innovative treatments for neurological conditions like epilepsy, and the ongoing pursuit of knowledge to improve patient care.
Could low vitamin D levels be silently impacting your heart health? New studies investigate the connection between vitamin D deficiency and increased cardiovascular risk factors, especially for individuals with metabolic syndrome. Discover what the science says.
Explore the transformative potential of integrating elderly individuals' perspectives and primary healthcare strategies in reshaping our understanding and approach to oral health, leading to improved care and well-being.
Could a simple smell test help identify individuals at risk of psychosis? A recent study investigates the connection between olfactory and cognitive functions in young Chinese adults, revealing a potential new avenue for early intervention in mental health.
Discover how scientists are harnessing the power of mRNA to boost keratinocyte growth, potentially leading to groundbreaking advancements in wound care and skin regeneration.
Explore the details of the first autochthonous Zika virus outbreak in Sabah, Malaysia. This article provides insights into the virus's transmission, potential sources, and the steps being taken to understand and control its spread.
Discover how a Korean family's struggle with progressive neurological symptoms led to a groundbreaking diagnosis of Hereditary Gelsolin Amyloidosis (HGA) through advanced genetic testing. Learn about the p.D214Y mutation in the GSN gene and its implications for early diagnosis and potential treatments for this rare condition.
