The "R" in C.A.R.E.S stands for RESEARCH!
Next week on February 10th and 11th we are going to literally “walk the talk” and go office to office…
Read MoreNext week on February 10th and 11th we are going to literally “walk the talk” and go office to office…
Read MoreWe have an URGENT request of anyone who is affected by multiple tumors from neurofibromatosis or has a loved one…
Read MoreOn February 10th and 11th, NF Midwest executive director Diana Haberkamp and others will be the visiting congressional offices of…
Read MoreThe Genetics Division at the Faculty of Medicine and Health Sciences from Université de Sherbrooke in Québec has opened a…
Read MoreA video released in January 2013 by the Congressionally Directed Medical Research Program (CDRMP) highlights the work of Dr. Karen Cichowski,…
Read MoreGenetic Evaluation for the Scoliosis Gene(s) in Patients with Neurofibromatosis 1 and Scoliosis Participants are needed for a study entitled:…
Read MoreCall for Study Participants The Department of Medical Genetics at Henry Ford Hospital in Detroit, MI is conducting a study…
Read MoreA neurofibromatosis type 2 researcher is looking for people who have been diagnosed with NF2 and have hearing loss to…
Read MoreCheck out the newest edition of the Network Edge provided by the Neurofibromatosis Network, NF Midwest’s national affiliate. This science column provides…
Read MoreThe Neurofibromatosis Network, NF Midwest’s national affiliate, has just unveiled their new science column called The Network Edge which will provide a…
Read More
© 2024 Neurofibromatosis Midwest - non profit 501(c)(t3). Site Map - Privacy Policy
The resources on this site should not be used as a substitute for professional medical care or advice on Neurofibromatosis. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional.