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Awareness
Time Magazine Highlights Industry’s Growing Interest in Rare Diseases
Awareness
Melanoma Drug Advance Has Broader Implications For Other Diseases
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Q&A with Dr. Kim Hunter-Schaedle
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FDA Funds Could Support Neurofibromatosis Clinical Trials
Awards & Grants
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Announcing the 2010 YIA Recipients
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5 Reasons to Sign Up for ctf.org
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Senate Bill Encourages Companies to Develop Rare Disease Drugs
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NF2-SWN
Science & Research
NF2’s Merlin Protein Finds a New Role – in the Liver
Awareness
CTF Offers $100K Clinical Research Awards: LOIs due Sept 15th
Awareness
NIH Director’s Program Could Fund Your Project to $25M a Year
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Recent Posts
Repurposed Drugs Offer Hope and Momentum for Rare Disease Treatments
Story of NF: Everly F.
“It’s not a sprint, it’s a marathon” – Brittany’s NF2-SWN Journey
Attention NF Researchers: New Federal Funding Opportunities Available
A Rare Connection at the NF Summit
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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
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