44:02

Webinar: How to Tell a Child about an NF1 Diagnosis?

00:40

Trailer: My Superpower, a CTF Short Documentary Film

58:05

CTF Engage: Gene-Targeted Therapy in NF

52:24

NF2-SWN Accelerator Meetup: Facial Reanimation Surgery

01:31

Cincinnati Shine A Light NF Walk

12:32

Storytelling: Leanna Scaglione at the 2024 NF Summit

01:22

CTF 2024 Global NF Conference Sizzle

09:49

My Superpower - A Short Documentary from the Children's Tumor Foundation

01:20

Children's Tumor Foundation Preclinical Hub

03:35

2024 May NF Awareness Month Recap

03:33

Why Join the NF Field? Working in Neurofibromatosis and Schwannomatosis Research

10:06

EFPIA Director General Nathalie Moll Delivers Opening Address at the Global NF Conference

01:46

This is NF. Living with Neurofibromatosis or Schwannomatosis.

01:20

Natural History Study of Cutaneous Neurofibromas in People with Neurofibromatosis Type 1 (NF1)

14:29

2017 von Recklinghausen Award

55:08

NF Summit 2022: Communication Technology in NF2 Panel

01:07:05

NF2-SWN Accelerator Meetup: Hearing Preservation and Restoration in NF2-related schwannomatosis

03:13

Make NF Visible: CJ and Sarah

00:31

Lindsey and Bryson Make NF Visible PSA

03:20

Shine A Light NF Walk 2023 Media Reel

01:09

Únase al Registro NF - Español (Subtítulos en español)

01:09

Join the NF Registry - Spanish (English Subtitles)

02:04

Using the NF Registry in Research

00:45

Children’s Tumor Foundation Rings The Opening Bell®

01:37

Make NF Research Visible: Carrie and Holly Beeman

01:48

The Time is Now: Philip Moss

02:45

Make NF Research Visible

50:49

NF Summit 2024: Welcome Dinner and Keynote with Josh Denny, MD, MS

56:08

NF2-SWN Accelerator Meetup: A Conversation with Matt Hay

02:08

Shine A Light NF Walk

49:46

NF Summit 2024: Hearing Preservation in NF2-SWN

47:08

NF Summit 2024: Vestibular Rehabilitation

14:10

NF Summit 2024: The Importance of Building Your Team: Interactive Workshop Session

40:36

NF Summit 2024: Hearing & Communication Technology

38:38

NF Summit 2024: Caregivers Need Care, Too: Exploring The Impact of Rare Disease on the Family

43:40

NF Summit 2024: Treatments for Cutaneous Neurofibromas: Where We Are Now and Where We Are Going

34:53

NF Summit 2024: Navigating Family Building When You Have Neurofibromatosis & Schwannomatosis

50:06

NF Summit 2024: How We Study Pain in Neurofibromatosis and Schwannomatosis

45:46

NF Summit 2024: Self Advocacy in Rare Disease

45:09

NF Summit 2024: Patient Engagement: Drug Development in Rare Disease

01:01:52

NF Summit 2024: The Storyteller Session

37:45

NF Summit 2024: Patient Engagement in NF Research

56:02

NF Summit 2024: Make NF Visible Awards Lunch

08:07

NF Summit 2024: Welcome to the NF Summit 2024!

48:37

NF Summit 2024: Thinking Big, Partnering for Success

01:04:19

NF Summit 2024: NF1 Through the Lifespan

29:23

NF Summit 2024: NF and School

28:02

NF Summit 2024: Improving Interpretation of Your Genetic Testing

29:00

NF Summit 2024: Keynote with Amit Ghose

10:00

Play It By Ear: A Short Documentary from the Children's Tumor Foundation

00:40

Trailer: My Superpower, a CTF Short Documentary Film

41:30

Phase 2b Study of NFX‑179 Topical Gel: A Webinar from NFlection Therapeutics

01:48

The Time is Now: Philip Moss

03:31

The Time is Now: 45 Years of Impact at the Children's Tumor Foundation

03:13

Quick Tour of CTF's NF & SWN Diagnosis Mobile App

56:29

NF2-SWN Meetup:How You Can Get Involved in CTF Engage

03:30

2024 CTF National Ambassador Kevin Martin

04:56

Latin American NF Conference | Introduction | Mislen Bauer, MD, Annette Bakker, PhD

43:21

Latin American NF Conference I Diagnostic Criteria I Scott Plotkin, MD, PhD

35:10

Latin American NF Conference | Cutaneous Neurofibromas | Carlos Romo, MD