184 related articles for article (PubMed ID: 15465081)
21. Histological evidence of redox system breakdown caused by superoxide dismutase 1 (SOD1) aggregation is common to SOD1-mutated motor neurons in humans and animal models.
Kato S; Saeki Y; Aoki M; Nagai M; Ishigaki A; Itoyama Y; Kato M; Asayama K; Awaya A; Hirano A; Ohama E
Acta Neuropathol; 2004 Feb; 107(2):149-58. PubMed ID: 14648077
[TBL] [Abstract][Full Text] [Related]
22. Absence of SOD1 gene abnormalities in familial amyotrophic lateral sclerosis with posterior column involvement without Lewy-body-like hyaline inclusions.
Kato S; Kawata A; Oda M; Arai N; Komori T; Tanabe H
Acta Neuropathol; 1996 Nov; 92(5):528-33. PubMed ID: 8922067
[TBL] [Abstract][Full Text] [Related]
23. An in vitro model for Lewy body-like hyaline inclusion/astrocytic hyaline inclusion: induction by ER stress with an ALS-linked SOD1 mutation.
Yamagishi S; Koyama Y; Katayama T; Taniguchi M; Hitomi J; Kato M; Aoki M; Itoyama Y; Kato S; Tohyama M
PLoS One; 2007 Oct; 2(10):e1030. PubMed ID: 17925878
[TBL] [Abstract][Full Text] [Related]
24. Sporadic amyotrophic lateral sclerosis and breast cancer: Hyaline conglomerate inclusions lead to identification of SOD1 mutation.
Hays AP; Naini A; He CZ; Mitsumoto H; Rowland LP
J Neurol Sci; 2006 Mar; 242(1-2):67-9. PubMed ID: 16423367
[TBL] [Abstract][Full Text] [Related]
25. Familial amyotrophic lateral sclerosis: a SOD1-unrelated Japanese family of bulbar type with Bunina bodies and ubiquitin-positive skein-like inclusions in lower motor neurons.
Tagawa A; Tan CF; Kikugawa K; Fukase M; Nakano R; Onodera O; Nishizawa M; Takahashi H
Acta Neuropathol; 2007 Feb; 113(2):205-11. PubMed ID: 17036243
[TBL] [Abstract][Full Text] [Related]
26. [Familial amyotrophic lateral sclerosis (FALS) with a novel SOD1 gene mutation: a clinicopathological study].
Kawamata C; Morita M; Shibata N; Nakano I
Rinsho Shinkeigaku; 2007 May; 47(5):211-6. PubMed ID: 17585602
[TBL] [Abstract][Full Text] [Related]
27. Sporadic amyotrophic lateral sclerosis with dementia and Cu/Zn superoxide dismutase-positive Lewy body-like inclusions.
Matsumoto S; Kusaka H; Ito H; Shibata N; Asayama T; Imai T
Clin Neuropathol; 1996; 15(1):41-6. PubMed ID: 8998856
[TBL] [Abstract][Full Text] [Related]
28. Clinical and pathological studies of familial amyotrophic lateral sclerosis (FALS) with SOD1 H46R mutation in large Japanese families.
Arisato T; Okubo R; Arata H; Abe K; Fukada K; Sakoda S; Shimizu A; Qin XH; Izumo S; Osame M; Nakagawa M
Acta Neuropathol; 2003 Dec; 106(6):561-8. PubMed ID: 14517684
[TBL] [Abstract][Full Text] [Related]
29. Familial amyotrophic lateral sclerosis with posterior column degeneration and basophilic inclusion bodies: a clinical, genetic and pathological study.
Tsuchiya K; Matsunaga T; Aoki M; Haga C; Ooe K; Abe K; Ikeda K; Nakano I
Clin Neuropathol; 2001; 20(2):53-9. PubMed ID: 11327297
[TBL] [Abstract][Full Text] [Related]
30. Familial amyotrophic lateral sclerosis with bulbar onset and a novel Asp101Tyr Cu/Zn superoxide dismutase gene mutation.
Tan CF; Piao YS; Hayashi S; Obata H; Umeda Y; Sato M; Fukushima T; Nakano R; Tsuji S; Takahashi H
Acta Neuropathol; 2004 Oct; 108(4):332-6. PubMed ID: 15235802
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Advanced glycation endproducts are deposited in neuronal hyaline inclusions: a study on familial amyotrophic lateral sclerosis with superoxide dismutase-1 mutation.
Shibata N; Hirano A; Kato S; Nagai R; Horiuchi S; Komori T; Umahara T; Asayama K; Kobayashi M
Acta Neuropathol; 1999 Mar; 97(3):240-6. PubMed ID: 10090670
[TBL] [Abstract][Full Text] [Related]
33. Neuropathological changes in two lines of mice carrying a transgene for mutant human Cu,Zn SOD, and in mice overexpressing wild type human SOD: a model of familial amyotrophic lateral sclerosis (FALS).
Dal Canto MC; Gurney ME
Brain Res; 1995 Apr; 676(1):25-40. PubMed ID: 7796176
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytes.
Kato S; Takikawa M; Nakashima K; Hirano A; Cleveland DW; Kusaka H; Shibata N; Kato M; Nakano I; Ohama E
Amyotroph Lateral Scler Other Motor Neuron Disord; 2000 Jun; 1(3):163-84. PubMed ID: 11464950
[TBL] [Abstract][Full Text] [Related]
36. α-Synuclein coaggregation in familial amyotrophic lateral sclerosis with SOD1 gene mutation.
Takei Y; Oguchi K; Koshihara H; Hineno A; Nakamura A; Ohara S
Hum Pathol; 2013 Jun; 44(6):1171-6. PubMed ID: 23352207
[TBL] [Abstract][Full Text] [Related]
37. Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase gene.
Cudkowicz ME; McKenna-Yasek D; Chen C; Hedley-Whyte ET; Brown RH
Ann Neurol; 1998 Jun; 43(6):703-10. PubMed ID: 9629839
[TBL] [Abstract][Full Text] [Related]
38. Phosphorylated Smad2/3 immunoreactivity in sporadic and familial amyotrophic lateral sclerosis and its mouse model.
Nakamura M; Ito H; Wate R; Nakano S; Hirano A; Kusaka H
Acta Neuropathol; 2008 Mar; 115(3):327-34. PubMed ID: 18210139
[TBL] [Abstract][Full Text] [Related]
39. Immunohistochemical study on superoxide dismutases in spinal cords from autopsied patients with amyotrophic lateral sclerosis.
Shibata N; Asayama K; Hirano A; Kobayashi M
Dev Neurosci; 1996; 18(5-6):492-8. PubMed ID: 8940623
[TBL] [Abstract][Full Text] [Related]
40. Colocalization of Bunina bodies and TDP-43 inclusions in a case of sporadic amyotrophic lateral sclerosis with Lewy body-like hyaline inclusions.
Miki Y; Mori F; Seino Y; Tanji K; Yoshizawa T; Kijima H; Shoji M; Wakabayashi K
Neuropathology; 2018 Oct; 38(5):521-528. PubMed ID: 29938835
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
