White matter disorders with autosomal dominant heredity: a review with personal clinical case studies and their MRI findings
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0404.2009.01219.x/fullpdf
Reference33 articles.
1. Leukoencephalopathy with vanishing white matter due to homozygous EIF2B2 gene mutation. First Polish cases;Mierzewska;Folia Neuropathol,2006
2. Nasu-Hakola disease (PLOSL): report of five cases and review of the literature;Madry;Clin Orthop Relat Res,2007
3. Adult onset MLD: a gene mutation with isolated polyneuropathy;Felice;Neurology,2000
4. Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease;Sourander;Acta Neuropathol,1977
5. Autosomal dominant diffuse leukoencephalopathy with neuroaxonal spheroids;van der Knaap;Neurology,2000
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