Treatment of Neurofibromatosis Type 1
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology
Link
http://link.springer.com/content/pdf/10.1007/s11940-015-0355-4.pdf
Reference73 articles.
1. Jett K, Friedman MJ. Clinical and genetic aspects of neurofibromatosis 1. Genet Med. 2010;12:1–11.
2. National Institutes of Health Consensus Development Conference Statement: Neurofibromatosis. Arch Neurol (Chicago). 1988;45:575–8.
3. DeBella K, Szudek J, Friedman JM. Use of the national institutes of health criteria for diagnosis of neurofibromatosis 1 in children. Pediatrics. 2000;105:608–14.
4. Stoll C. Difficulties in the diagnosis of neurofibomatosis-1 in children. Am J Med Genet. 2002;112:422–6.
5. Tadini G, Milani D, Menni F, et al. Is it time to change the neurofibromatosis type 1 diagnostic criteria? Eur J Intern Med. 2014;25:506–10. An interesting paper that provides emerging criteria useful for a precocious diagnosis of NF1 in paediatric age.
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