Cerebral vasculopathy in a Chinese family with neurofibromatosis type I mutation-Reference-Cited by-同舟云学术

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Cerebral vasculopathy in a Chinese family with neurofibromatosis type I mutation

Published:2013-11-11 Issue:6 Volume:29 Page:708-714
ISSN:1673-7067
Container-title:Neuroscience Bulletin
language:en
Short-container-title:Neurosci. Bull.

Author:

Liang Jian-Tao,Huo Li-Rong,Bao Yu-Hai,Wang Zhen-Yu,Ling Feng

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Physiology,General Neuroscience

Link

http://link.springer.com/content/pdf/10.1007/s12264-013-1388-x.pdf

Reference25 articles.

1. Rasmussen SA, Friedman JM. NF1 gene and neurofibromatosis 1. Am J Epidemiol 2000, 151: 33–40.

2. Viskochil D, Buchberg AM, Xu G, Cawthon RM, Stevens J, Wolff RK, et al. Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus. Cell 1990, 62: 187–192.

3. Friedman JM, Birch PH. Type 1 neurofibromatosis: a descriptive analysis of the disorder in 1,728 patients. Am J Med Genet 1997, 70: 138–143.

4. Tang SC, Lee MJ, Jeng JS, Yip PK. Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke. J Neurol Sci 2006, 243: 53–55.

5. Hamilton SJ, Friedman JM. Insights into the pathogenesis of neurofibromatosis 1 vasculopathy. Clin Genet 2000, 58: 341–344.

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3. Transcranial Doppler ultrasound in children with stroke and cerebrovascular disorders;Current Opinion in Pediatrics;2015-12

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