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Story of NF: Ivan R.
1 day ago
in:
NF1
,
Story of NF
no comments
The Friedrich von Recklinghausen Award: Neurofibromatosis Tradition and Progress
5 days ago
in:
Awards & Grants
,
Featured
,
Featured EU
no comments
The Future of Rare Disease Starts Here: NF Leaders Gather in Washington, D.C.
1 week ago
in:
Featured
,
Featured EU
,
Press Release
no comments
Listen In: How CTF Is Shaping the Future of NF Drug Development
1 week ago
in:
CTF in the News
,
Science & Research
no comments
CTF CEO Annette Bakker to Speak on Drug Development Panel at BIO 2025
1 week ago
in:
Science & Research
no comments
Help Fill the Gap to Fuel NF Research and Care
2 weeks ago
in:
Featured
,
Featured EU
,
Science & Research
no comments
Story of NF: Jenelle B.
2 weeks ago
in:
Story of NF
no comments
NFE Athlete Spotlight: Matthew Haas
2 weeks ago
in:
Featured
,
Featured EU
,
NF Endurance
,
NF1
,
Ways to Give
no comments
Your Voice Was Heard: $25 Million for NF Research Proposed in New House Bill
2 weeks ago
in:
Advocacy
,
Top Story
,
Top Story EU
no comments
Repurposed Drugs Offer Hope and Momentum for Rare Disease Treatments
3 weeks ago
in:
CTF in the News
,
Science & Research
no comments
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Learn About NF
Understanding NF
Neurofibromatosis Type 1
NF2
-Related Schwannomatosis
Schwannomatosis
Newly Diagnosed
Café Au Lait Spots
Genetics of NF
NF In Our Culture
Life With NF
Find a Doctor
NF Treatments
NF Registry
Resource Center
NF Summit
Educational Events
Patient Engagement
Clinical Trials
Clinicians
Diagnostic Criteria
NF Clinic Network (NFCN)
Conferences & Education
Partnerships
Clinical Trials Pipeline
Researchers
Funding Opportunities
Conferences & Education
Research Tools & Resources
Leading Minds in NF Research
Pharma
For Pharma & Biotech
Industry Partnerships
Our Impact
Our Mission
Our Impact
Our Portfolio
About CTF
Our Strategy
Take Action
Ways to Give
Events & Fundraisers
Raise Awareness
Advocacy
Volunteer
Share Your Story
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