Current progress in genomics and targeted therapies for neurofibromatosis type 2
Author:
Affiliation:
1. Department of Neurosurgery, Fukushima Medical University
2. Department of Neurosurgery, Fukushima Rosai Hospital
Publisher
The Fukushima Society of Medical Science
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/fms/69/2/69_2023-05/_pdf
Reference55 articles.
1. 1. Evans DG, Moran A, King A, Saeed S, Gurusinghe N, Ramsden R. Incidence of vestibular schwannoma and neurofibromatosis 2 in the North West of England over a 10-year period:higher incidence than previously thought. Otol Neurotol, 26:93-97, 2005.
2. 2. Evans DG. Neurofibromatosis type 2 (NF2):a clinical and molecular review. Orphanet J Rare Dis, 4:16, 2009.
3. 3. Iwatate K, Yokoo T, Iwatate E, Ichikawa M, Sato T, Fujii M, et al. Population Characteristics and Progressive Disability in Neurofibromatosis Type 2. World Neurosurg, 106:653-660, 2017.
4. 4. Otsuka G, Saito K, Nagatani T, Yoshida J. Age at symptom onset and long-term survival in patients with neurofibromatosis Type 2. J Neurosurg, 99:480-483, 2003.
5. 5. Evans DG, Huson SM, Donnai D, Neary W, Blair V, Teare D, et al. A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity. J Med Genet, 29:841-846, 1992.
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