Burden Among Caregivers of Pediatric Patients with Neurofibromatosis Type 1 (NF1) and Plexiform Neurofibroma (PN) in the United States: A Cross-Sectional Study. [PDF]
Yang X +6 more
europepmc +1 more source
Innovation in the treatment of persistent pain in adults with Neurofibromatosis Type 1 (NF1): Implementation of the iCanCope mobile application. [PDF]
Buono FD +7 more
europepmc +1 more source
Risk Factors for Bullying Victimization in Children with Neurofibromatosis Type 1 (NF1). [PDF]
Stavinoha PL +5 more
europepmc +1 more source
Population pharmacokinetics of FCN-159, a MEK1/2 inhibitor, in adult patients with advanced melanoma and neurofibromatosis type 1 (NF1) and model informed dosing recommendations for NF1 pediatrics. [PDF]
Tan Y +8 more
europepmc +1 more source
A novel neurofibromatosis type 1 (NF1) mutation in a patient with NF1 and pheochromocytoma [PDF]
Seo, Yoorim +6 more
openaire +1 more source
Increased risk of breast cancer in neurofibromatosis type 1: current insights
Sacha J Howell,1 Kimberley Hockenhull,1 Zena Salih,1 D Gareth Evans2,3 1Department of Medical Oncology, The Christie NHS Foundation Trust, 2Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health,
Howell SJ +3 more
doaj
Selection of internal references for RT-qPCR assays in Neurofibromatosis type 1 (NF1) related Schwann cell lines. [PDF]
Gu YH +11 more
europepmc +1 more source
Identifying Bone Matrix Impairments in a Mouse Model of Neurofibromatosis Type 1 (NF1) by Clinically Translatable Techniques. [PDF]
Ahmed R +6 more
europepmc +1 more source
A neurofibromatosis type 1 family report with multiple cases in 3 consecutive Generations
Neurofibromatosis type1 (NF1) with the incidence of 1 in 3500 births, is the most common disorder which affects skin and peripheral nervous system. NF1 results from mutations in NF1 gene. The NF1 gene spans 350kbp and to date, nearly 2434 mutations in it
M Oladnabi +4 more
doaj
A Novel Neurofibromatosis Type 1 (NF1) Frameshift Mutation Associated With Atypical Hypotensive Pheochromocytoma: A Case Report. [PDF]
Kotan R, Göçer EG, Koç MS.
europepmc +1 more source

