Search Results 61-70 of 22332 for neurofibromatosis
Examples of these include multiple endocrine neoplasia, type 1 (MEN 1), von Hippel-Lindau (VHL) disease, neurofibromatosis 1 (NF1) and tuberous sclerosis.
Mayo Clinic's Neurofibromatosis Type 2 Clinic provides expert, multidisciplinary care for teenagers and adults with this tumor-predisposing genetic disorder.
Neurofibromatosis; Osteogenesis imperfecta; Piebaldism; Progeria; Pseudoxanthoma elasticum; PTEN hamartoma tumor syndrome, including Cowden syndrome; Skin ...
She studies and reports new findings in rare genetic disorders and neurocutaneous disorders with focus on neurofibromatosis and schwannomatosis. Dr. Dhamija ...
Some ependymomas are linked to genetic conditions passed down in families, such as with neurofibromatosis type 2 and Li-Fraumeni syndrome. The Mayo Clinic ...
Neurofibroma development in neurofibromatosis type 1: Insights from cellular origin and Schwann cell lineage development. Cancers. 2022; doi:10.3390 ...
... neurofibromatosis. The diagnosis Dr. Dhamija thought of when she met Cameron was schwannomatosis, which is similar to neurofibromatosis, but allows for the ...
... Neurofibromatosis and Low-Grade Glioma Rochester, MN. The pupose of this study is to evaluate whether or not selumetinib works just as well as the standard ...
Multiple endocrine neoplasia, type 1 (MEN 1); Multiple endocrine neoplasia, type 2 (MEN 2); Von Hippel-Lindau disease; Tuberous sclerosis; Neurofibromatosis ...
Neurofibromatosis Type 2 Clinic · Neurology · Neurosurgery · Otolaryngology (ENT)/Head and Neck Surgery · Pediatric Hematology/Oncology · Radiation Oncology ...
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