Lhermitte–Duclos Disease: Case Report and Literature Review
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Publisher
Jaypee Brothers Medical Publishing
Link
https://www.ijhns.com/doi/pdf/10.5005/jp-journals-10001-1424
Reference11 articles.
1. 1. Nowak DA, Trost HA. Lhermitte-Duclos disease (dysplasticcerebellar gangliocytoma): a malformation, hamartoma or neoplasm? Acta Neurol Scand 2002;105(3):137–145. DOI: 10.1034/j.1600-0404.2002.1r127.x.
2. 2. Andres RH, Guzman R, Weis J, et al. Lhermitte-Duclos disease with atypical vascularization - case report and review of the literature. Clin Neuropathol 2009;28(03):83–90. DOI: 10.5414/NPP28083.
3. 3. Ishizaki K, Daita G, Yonemasu Y, et al. Hypervascularity in Lhermitte-Duclos disease-case report. Neurol Med Chir (Tokyo) 1997;37(5):403–406. DOI: 10.2176/nmc.37.403.
4. 4. Moonis G, Ibrahim M, Melhem ER. Diffusion-weighted MRI in Lhermitte-Duclos disease: report of two cases. Neuroradiology 2004;46(5):351–354. DOI: 10.1007/s00234-004-1190-6.
5. 5. Afshar-Oromieh A, Linhart H, Podlesek D, et al. Postoperative cerebellar mutism in adult patients with Lhermitte-Duclos disease. Neurosurg Rev 2010;33(4):401–408. DOI: 10.1007/s10143-010- 0278-1.
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