Primary lateral sclerosis: a rare upper-motor-predominant form of amyotrophic lateral sclerosis often accompanied by frontotemporal lobar degeneration with ubiquitinated neuronal inclusions?-Reference-Cited by-同舟云学术

Primary lateral sclerosis: a rare upper-motor-predominant form of amyotrophic lateral sclerosis often accompanied by frontotemporal lobar degeneration with ubiquitinated neuronal inclusions?

Published:2003-03-01 Issue:6 Volume:105 Page:615-620
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Tan Chun-Feng,Kakita Akiyoshi,Piao Yue-Shan,Kikugawa Koki,Endo Kotaro,Tanaka Masami,Okamoto Koichi,Takahashi Hitoshi

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00401-003-0687-0.pdf

Reference35 articles.

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3. Erb WH (1875) Über einen wenig bekannten spinalen Symptomenkomplex. Klin Wochenschr 12:357–359

4. Fisher CM (1977) Pure spastic paralysis of corticospinal origin. Can J Neurol Sci 4:251–258

5. Holton JL, Révész T, Crooks R, Scaravilli F (2002) Evidence for pathological involvement of the spinal cord in motor neuron disease-inclusion dementia. Acta Neuropathol 103:221–227

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