LEXINGTON, Mass.--(BUSINESS WIRE)--Orphan Technologies, a company dedicated to helping patients control their homocysteine levels, today announced that OT-58 for the treatment of cystathionine beta ...

This page lists all known medications that could potentially lead to 'Homocystinuria' as a side effect. It's important to note that mild side effects are quite common with medications. The ...

Homocystinuria (McKusick 236200) due to cystathionine B-synthase (EC 4.2.1.22) deficiency is an inborn error of transsulfuration metabolism. The major biochemical ...

HCU is a rare autosomal recessive inherited sulfur amino acid metabolism disorder primarily caused by a cystathionine beta-synthase deficiency (CBS). HCU patients have a broad spectrum of age (older ...

Dublin, Dec. 18, 2024 (GLOBE NEWSWIRE) -- The "Homocystinuria - Pipeline Insight, 2024" drug pipelines has been added to ResearchAndMarkets.com's offering. This report provides comprehensive insights ...

Established by the Qatar Foundation for Education, Science, and Community Development, Sidra Medicine is committed to ...

The University of Colorado (CU) has signed exclusive, worldwide licensing and collaboration agreements with rare-disease research-and-development firm Orphan Technologies Ltd to develop an enzyme ...

Dublin, June 14, 2022 (GLOBE NEWSWIRE) -- The "Homocystinuria - Market Insight, Epidemiology and Market Forecast -2032" report has been added to ResearchAndMarkets.com's offering. The report delivers ...

Doha, Qatar: A recent research study conducted by members of Qatar University’s (QU) Health Sector titled “Pathogenic Homocystinuria-Associated T236N Mutation Dramatically Alters the Biochemical ...

In a new paper, researchers describe finding the gene that causes Mexican cavefish to lose their vision. The same gene responsible for this evolutionary change in the fish is also responsible for ...