PMID: 6410004Jun 1, 1983Paper

Neurophysiological findings in the hereditary presenile dementia characterised by polycystic lipomembranous osteodysplasia and sclerosing leukoencephalopathy

Journal of Neurology, Neurosurgery, and Psychiatry
H P Hakola, V S Partanen

Abstract

17 patients suffering from the presenile dementia characterised by polycystic lipomenbranous osteodysplasia and sclerosing leukoencephalopathy were studied neurophysiologically. Noteworthy findings were diffuse slowing, the accentuation of 6-8 Hz parasagittal activity, slowing of the dominant occipital rhythm and, in the late phase when 13 of patients got epileptic seizures, there was paroxysmal activity in the EEG.

References

Apr 1, 1977·Neurology·P GloorN Schaul
May 20, 1982·The New England Journal of Medicine·K H Chiappa, A H Ropper
Jan 1, 1982·Acta Neurologica Scandinavica·H SoininenP J Riekkinen
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Aug 1, 1981·Journal of Computer Assisted Tomography·E M Laasonen, U Lahdenranta
Jan 1, 1980·Acta Neuropathologica·J Tanaka

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Citations

Jan 1, 1991·Virchows Archiv. A, Pathological Anatomy and Histopathology·Y MiiS Tamai
Jan 1, 1990·Virchows Archiv. A, Pathological Anatomy and Histopathology·R Machinami
Oct 19, 2000·Neuropathology : Official Journal of the Japanese Society of Neuropathology·J Tanaka

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