Survey for Parents of Children with NF1
Dr. Maria Acosta at Children’s National Medical Center is looking for parents of children with Neurofibromatosis Type 1 in which…
Read MoreDr. Maria Acosta at Children’s National Medical Center is looking for parents of children with Neurofibromatosis Type 1 in which…
Read MoreNF Midwest has previously funded studies by Dr. Klein-Tasman’s team that has resulted in valuable information on the cognitive abilities…
Read MoreWe are conducting an important survey of patients with NF1 about electrosurgical removal of neurofibromas (dermal (cutaneous)) and/or subcutaneous tumors…
Read MoreCollaborators from the University of Wisconsin – Dept. of Psychology have published a THIRD paper based on cognitive studies of…
Read MoreWe are proud to learn that Christy Casnar, a collaborator on an ongoing study that NF Midwest has funded for…
Read MoreIt can be challenging to gather information from enough people for neurofibromatosis type 1 research. Having a large number of…
Read MoreMembers of NF Midwest, NF Northeast and Texas NF visited Cold Spring Harbor laboratory in New York in the…
Read MoreWe are excited and proud to announce our collaboration with the University of Wisconsin-Madison, Biotechnology Center. The UW Biotechnology Center…
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…
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