Author:
Nishibayashi Fumiko,Kawashima Miho,Katada Yoshiaki,Murakami Nobuyuki,Nozaki Miwako
Publisher
Springer Science and Business Media LLC
Reference7 articles.
1. Murakami N, Tsuchiya T, Kanazawa N, Tsujino S, Nagai T: Novel deletion mutation in GFAP gene in an infantile form of Alexander Disease. Pediatr Neurol. 2008, 38: 50-52. 10.1016/j.pediatrneurol.2007.08.017.
2. van der Knaap MS, Naidu S, Breiter SN, Blaser S, Stroink H, Springer S, Begeer JC, van Coster R, Barth PG, Thomas NH, Valk J, Powers JM: Alexander Disease: Diagnosis with MR imaging. Am J Neuroradiol. 2001, 22: 541-552.
3. Sakakibara T, Takahashi Y, Fukuda K, Inoue T, Kurosawa T, Nishikubo T, Shima M, Taoka T, Aida N, Tsujino S, Kanazawa N, Yoshioka A: A case of infantile Alexander disease diagnosed by magnetic resonance imaging and genetic analysis. Brain Dev. 2007, 29: 525-528. 10.1016/j.braindev.2007.02.002.
4. Yoshida T, Nakagawa M: Clinical aspects and pathology of Alexander disease, and morphological and functional alteration of astrocytes induced by GFAP mutation. Neuropathol. 2012, 32: 440-446. 10.1111/j.1440-1789.2011.01268.x.
5. Yoshida T, Sasaki M, Yoshida M, Namekawa M, Okamoto Y, Tsujino S, Sasayama H, Mizuta I, Nakagawa M, The Alexander Disease Study Group in Japan: Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosis. J Neurol. 2011, 258: 1998-2008. 10.1007/s00415-011-6056-3.
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献