Case Studies

Poster: Alpha-1 Antitrypsin Deficiency: Why millions remain undiagnosed

Alpha-1 antitrypsin deficiency (AATD), a rare genetic condition, can cause lung disease in adults with symptoms similar to chronic obstructive

Finding Patients for Rare Diseases: A Case Study

By Christopher Rudolf, Volv Global An AI methodology for finding patients with rare diseases: Volv Global’s inTrigue The Case

Case Study: Detecting signs of Fabry and Pompe disease in UK clinical data

Volv, supported by Sanofi, and working with Optimum Patient Care, and collaborating with a specialist Consultant Clinician, is performing research

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