Heather B. Radtke

Jaffe–Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder

Douglas R. Stewart, Hilde Brems, Alicia Gomes et al. · Genetics in Medicine · 2013 · 50 citations · Full text

Type 1, Molecular Analyses, Neurobiology Of Disease +6

Increasing access to specialty care for rare diseases: a case study using a foundation sponsored clinic network for patients with neurofibromatosis 1, neurofibromatosis 2, and schwannomatosis

Vanessa L. Merker, Annie Dai, Heather B. Radtke et al. · BMC Health Services Research · 2018 · 49 citations · Full text

Genetic Counseling for Neurofibromatosis 1, Neurofibromatosis 2, and Schwannomatosis—Practice Resource of the National Society of Genetic Counselors

Heather B. Radtke, Amanda L. Bergner, Allison L. Goetsch et al. · Journal of Genetic Counseling · 2020 · 27 citations · Full text

The impact of the COVID-19 pandemic on neurofibromatosis clinical care and research

Heather B. Radtke, Bonnie Klein-Tasman, Vanessa L. Merker et al. · Orphanet Journal of Rare Diseases · 2021 · 26 citations · Full text

Transition Readiness Assessment in Adolescents and Young Adults with Neurofibromatosis Type 1 (NF1)

Allison L. Goetsch, Tina Haws, Joanna Lee et al. · Comprehensive Child and Adolescent Nursing · 2020 · 16 citations