NORD and the Galactosemia Foundation Jointly Publish First “Voice of the Patient” Report to Help Inform the FDA and Researchers - National Organization for Rare Disorders
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Last updated 10 junho 2024
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National Organization for Rare Disorders - Overview, News
Galactosemia Foundation
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Fibrous Dysplasia Foundation and NORD Launch Cutting-Edge Study of
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Scholarship Foundation. of Santa Barbara Report to our Community
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Scholarship Foundation. of Santa Barbara Report to our Community
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Highlights from the 2022 NORD Breakthrough Summit - National
GLOW for Galactosemia Race & Family Event
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Scholarship Foundation. of Santa Barbara Report to our Community
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Writing the Book on Your Child's Rare Disease: Raymond's Story in
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New England Revolution on X: Wishing our very own Richie Williams
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NORD Launches Rare Disease Educational Support Program - National
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