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Angela Schulz, M.D., Temitayo Ajayi, M.D., Nicola Specchio, M.D., Ph.D., Emily de Los Reyes, M.D., Paul Gissen, M.B., Ch.B., Ph.D., Douglas Ballon, Ph.D., Jonathan P. Dyke, Ph.D., Heather Cahan, M.D., Peter Slasor, Sc.D., David Jacoby, M.D., Ph.D., and Alfried Kohlschütter, M.D., for the CLN2 Study Group

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Supporting Women at BioMarin: An Interview with the Co-Chairs of Our Women’s Leadership Development Group

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Sustainability Accounting Standards Board (SASB) 2022 Index

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Experiences of children and adolescents living with achondroplasia and their caregivers

Renée Shediac, Olga Moshkovich, Heather Gerould, Rachel Ballinger, Agnes Williams, M. Alex Bellenger, Jennifer Quinn, Julie Hoover-Fong, Klaus Mohnike, Ravi Savarirayan, Dominique Kelly

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Athena Countouriotis

Global Compliance and Ethics Program

Assessing the potential cost-effectiveness of a gene therapy for the treatment of hemophilia A

Systematic Review and Meta-Analysis of Neuropsychiatric Symptoms and Executive Functioning in Adults With Phenylketonuria

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Caring for Children with Achondroplasia: An Interview with Dr. Ciara McDonnell

At the Intersection of Science and Art

Howard University Partners with BioMarin on Regulatory Fellowship

The Unforgettable Moments from ‘The Style Show: A Runway to Empower’

The Three Lessons I’ve Learned from Planning a Fashion Show That Are Applicable to Life

It’s Time to Give a Platform, or in My Case “Runway,” to People with Rare Disease

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BioMarin Community Guidelines

Study of Intraventricular Cerliponase Alfa for CLN2 Disease