Cancer of the Peripheral Nerve in Neurofibromatosis Type 1

Author:

Staedtke Verena,Bai Ren-Yuan,Blakeley Jaishri O’Neill

Funder

Francis S. Collins Scholar Program

Children's Tumor Foundation

National Cancer Institute

Neurofibromatosis Therapeutic Acceleration Program

Bloomberg and Gottesman Foundation

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Clinical Neurology,Pharmacology

Reference73 articles.

1. Carey JC, Baty BJ, Johnson JP, Morrison T, Skolnick M, Kivlin J. The genetic aspects of neurofibromatosis. Ann N Y Acad Sci 1986; 486: 45-56.

2. NIH. National Institutes of Health Consensus Development Conference Statement: neurofibromatosis. Bethesda, Md., USA, July 13–15, 1987. Neurofibromatosis 1988; 1: 172-178.

3. Gutmann DH, Aylsworth A, Carey JC, et al. The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2. JAMA 1997; 278: 51-57.

4. Abramowicz A, Gos M. Neurofibromin in neurofibromatosis type 1—mutations in NF1gene as a cause of disease. Dev Period Med 2014; 18: 297-306.

5. Ratner N, Miller SJ. A RASopathy gene commonly mutated in cancer: the neurofibromatosis type 1 tumour suppressor. Nat Rev Cancer 2015; 15: 290-301.

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