These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Histochemical and immunocytochemical study of ubiquitinated neuronal inclusions in amyotrophic lateral sclerosis. Mather K; Martin JE; Swash M; Vowles G; Brown A; Leigh PN Neuropathol Appl Neurobiol; 1993 Apr; 19(2):141-5. PubMed ID: 8391129 [TBL] [Abstract][Full Text] [Related]
4. Asymmetric involvement of the spinal cord involving both large and small anterior horn cells in a case of familial amyotrophic lateral sclerosis. Kato T; Hirano A; Kurland LT Clin Neuropathol; 1987; 6(2):67-70. PubMed ID: 3036409 [TBL] [Abstract][Full Text] [Related]
5. Relationship between Bunina bodies and TDP-43 inclusions in spinal anterior horn in amyotrophic lateral sclerosis. Mori F; Tanji K; Miki Y; Kakita A; Takahashi H; Wakabayashi K Neuropathol Appl Neurobiol; 2010 Jun; 36(4):345-52. PubMed ID: 20345649 [TBL] [Abstract][Full Text] [Related]
6. The Golgi apparatus is fragmented in spinal cord motor neurons of amyotrophic lateral sclerosis with basophilic inclusions. Fujita Y; Okamoto K; Sakurai A; Kusaka H; Aizawa H; Mihara B; Gonatas NK Acta Neuropathol; 2002 Mar; 103(3):243-7. PubMed ID: 11907804 [TBL] [Abstract][Full Text] [Related]
8. An autopsy case of familial amyotrophic lateral sclerosis with a TARDBP Q343R mutation. Okamoto K; Fujita Y; Hoshino E; Tamura Y; Fukuda T; Hasegawa M; Takatama M Neuropathology; 2015 Oct; 35(5):462-8. PubMed ID: 26096467 [TBL] [Abstract][Full Text] [Related]
9. FUS/TLS-immunoreactive neuronal and glial cell inclusions increase with disease duration in familial amyotrophic lateral sclerosis with an R521C FUS/TLS mutation. Suzuki N; Kato S; Kato M; Warita H; Mizuno H; Kato M; Shimakura N; Akiyama H; Kobayashi Z; Konno H; Aoki M J Neuropathol Exp Neurol; 2012 Sep; 71(9):779-88. PubMed ID: 22878663 [TBL] [Abstract][Full Text] [Related]
10. Familial amyotrophic lateral sclerosis with onset in bulbar sign, benign clinical course, and Bunina bodies: a clinical, genetic, and pathological study of a Japanese family. Tsuchiya K; Shintani S; Nakabayashi H; Kikugawa K; Nakano R; Haga C; Nakano I; Ikeda K; Tsuji S Acta Neuropathol; 2000 Dec; 100(6):603-7. PubMed ID: 11078211 [TBL] [Abstract][Full Text] [Related]
11. Familial amyotrophic lateral sclerosis with an I104F mutation in the SOD1 gene: Multisystem degeneration with neurofilamentous aggregates and SOD1 inclusions. Jiang H; Shimizu H; Shiga A; Tanaka M; Onodera O; Kakita A; Takahashi H Neuropathology; 2017 Feb; 37(1):69-77. PubMed ID: 27444855 [TBL] [Abstract][Full Text] [Related]
12. Hereditary amyotrophic lateral sclerosis. Histochemical and electron microscopic study of hyaline inclusions in motor neurons. Takahashi K; Nakamura H; Okada E Arch Neurol; 1972 Oct; 27(4):292-9. PubMed ID: 4115557 [No Abstract] [Full Text] [Related]
13. HtrA2/Omi-immunoreactive intraneuronal inclusions in the anterior horn of patients with sporadic and Cu/Zn superoxide dismutase (SOD1) mutant amyotrophic lateral sclerosis. Kawamoto Y; Ito H; Kobayashi Y; Suzuki Y; Akiguchi I; Fujimura H; Sakoda S; Kusaka H; Hirano A; Takahashi R Neuropathol Appl Neurobiol; 2010 Jun; 36(4):331-44. PubMed ID: 20202124 [TBL] [Abstract][Full Text] [Related]
14. Stepwise acquirement of hallmark neuropathology in FUS-ALS iPSC models depends on mutation type and neuronal aging. Japtok J; Lojewski X; Naumann M; Klingenstein M; Reinhardt P; Sterneckert J; Putz S; Demestre M; Boeckers TM; Ludolph AC; Liebau S; Storch A; Hermann A Neurobiol Dis; 2015 Oct; 82():420-429. PubMed ID: 26253605 [TBL] [Abstract][Full Text] [Related]
15. Accumulation of neurofilaments and SOD1-immunoreactive products in a patient with familial amyotrophic lateral sclerosis with I113T SOD1 mutation. Kokubo Y; Kuzuhara S; Narita Y; Kikugawa K; Nakano R; Inuzuka T; Tsuji S; Watanabe M; Miyazaki T; Murayama S; Ihara Y Arch Neurol; 1999 Dec; 56(12):1506-8. PubMed ID: 10593307 [TBL] [Abstract][Full Text] [Related]
16. Maturation process of TDP-43-positive neuronal cytoplasmic inclusions in amyotrophic lateral sclerosis with and without dementia. Mori F; Tanji K; Zhang HX; Nishihira Y; Tan CF; Takahashi H; Wakabayashi K Acta Neuropathol; 2008 Aug; 116(2):193-203. PubMed ID: 18560845 [TBL] [Abstract][Full Text] [Related]
17. Involvement of Onuf's nucleus in ALS. Demonstration of intraneuronal conglomerate inclusions and Bunina bodies. Kihira T; Yoshida S; Uebayashi Y; Yase Y; Yoshimasu F J Neurol Sci; 1991 Aug; 104(2):119-28. PubMed ID: 1658239 [TBL] [Abstract][Full Text] [Related]
18. TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation. Tan CF; Eguchi H; Tagawa A; Onodera O; Iwasaki T; Tsujino A; Nishizawa M; Kakita A; Takahashi H Acta Neuropathol; 2007 May; 113(5):535-42. PubMed ID: 17333220 [TBL] [Abstract][Full Text] [Related]
19. [Histopathological and immunohistochemical study of spinal cord tissues in neurodegenerative diseases]. Zhu M; Wang L; Liu J; Gui Q; Guo Y; Hu Y; Zhang H Zhonghua Bing Li Xue Za Zhi; 2015 Aug; 44(8):587-93. PubMed ID: 26705184 [TBL] [Abstract][Full Text] [Related]