Related Articles
What AHRQ Learned While Working to Transform Primary Care
Building on previous efforts to transform primary care, the Agency for Healthcare Research and Quality (AHRQ) launched EvidenceNOW: Advancing Heart Health in 2015. This 3-year…
Quantifying methane emissions from United States landfills
Landfills across the United States emit substantial amounts of methane.
Alpha-Mannosidosis: Disease Overview, Signs and Symptoms, Emerging Therapies
Alpha-mannosidosis is a rare genetic disorder characterized by a deficiency of the enzyme alpha-D-mannosidase.
Tenosynovial Giant Cell Tumors (TGCT) Explained
Richard F. Riedel, MD, Medical Oncologist, Duke Health, discusses tyenosynovial giant cell tumors (TGCT)
Treatments for Biliary Tract Cancer
Robin Kate Kelley, MD, Professor of Clinical Medicine Hematology/IOncology, University of California, San Francisco, describes the need for better treatment plans for patients with biliary…
Rett Syndrome
Rett syndrome is a multisystem disorder that primarily affects girls; multiple loss-of-function mutations to the MECP2 gene are the cause of this rare disease.
Loader
We have noticed an unusual activity from your IP 199.16.157.183 and blocked access to this
March 21, 2024 | NEJM
Image Challenge from the New England Journal of Medicine — March 21, 2024
The PCF Women in Science Forum: Empowering Female Researchers Through Networking and Mentorship – Veda Giri, Ayesha Shafi, & Claire Fletcher
Andrea Miyahira hosts a discussion with Veda Giri, Ayesha Shafi, and Claire Fletcher, members of the PCF Women in Science Forum Organizing Committee. The forum…
Multi-Ancestry Genetic Study of Parkinson’s Disease Identifies New Risk Genes in Pursuit of Novel Treatment Targets
International collaboration is most genetically diverse study of the disease to date