Cases with familial diffuse leukoencephalopathy
Author:
Affiliation:
1. Psychogeriatric Center, Daigo Hospital, Mimata
2. Department of Psychiatry, Inoue Hospital, Miyazaki
Publisher
The Kyushu Association of Neuropsychiatry
Subject
General Earth and Planetary Sciences,General Environmental Science
Link
https://www.jstage.jst.go.jp/article/kyushuneurop/67/3_4/67_80/_pdf
Reference18 articles.
1. 1) Nasu, T.: General pathology of membranous lipodystrophy. In: Yonezawa, T. editor. International symposium on the leukoencepalopathy and allied diseases. Kyoto: The Japanese Society of Neuropathology, Pp.61-78, 1981.
2. 2) Hakola, H. P. A., Jarvi, O. H., Sourander, P.: Osteodysplasia polycystica herediteria combined with sclerosing leukoencepahopathy, a new entity of the dementia praesenilis group. Acta Neurol Scand Suppl, 46:79-80, 1970.
3. 3) 小柳清光,木下通亭:Nasu-Hakola病:ミクログリアと破骨細胞異常による脳白質変性と骨病変.神経内科,89:91-98,2018.
4. 4) Bianchin, M. M., Capella, H. M., Chaves, D. L. et al.: Nasu-Hakola disease (polycystic lipomembraneous osteodysplasia with sclerosing leukoencephalopathy; PLOS): a dementia associated with bone cystic lesions. From clinical to genetic and molecular aspects. Cell Mol Neurobiol, 24:1-24, 2004.
5. 5) Hakola, H. P. A.: Neuropsychiatric and genetic aspects of a new hereditary disease characterized by progressive dementia and liopomembraneous polycystic osteodysplasia. Acta Psychiatr Scand Suppl, 232:1-173, 1972.
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