Berkeley health officials are urging people to vacate a homeless encampment after an outbreak of a rare disease that can ...
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Former Little Mix star says doctors told her twin babies may never walk due to rare disease
When Jesy Nelson shared an emotional Instagram video in January 2026, the former Little Mix singer did more than reveal a ...
Advancements in the form of recent approvals and an evolving pipeline landscape in dermatology will bolster Leo’s chance of ...
Danish dermatology specialist Leo Pharma and its CEO Christophe Bourdon came to San Francisco to attend the J.P. Morgan ...
The FDA previously rejected Zycubo for Menkes disease in October last year, citing issues with the drug’s manufacturing ...
After years stuck in the “doldrums,” the biopharma sector is in a “very good place” heading into the new year, analysts told ...
Lozano is a rare disease mom, neuroscience Ph.D. candidate at UC Davis, and board member for the PURA Syndrome Foundation. In May, a historic moment in science and medicine was captured in a single ...
As someone living with a rare disease in Ohio, I know how fragile access to life-saving treatment can be. A bill to help patients with rare or life-threatening illnesses is currently being debated in ...
The Priority Review Voucher (PRV) program is designed to incentivize rare disease drug development.
The Republic of Serbia allocates millions for the treatment of rare diseases, and in 2025 alone, more than 930 patients in ...
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