195 related articles for article (PubMed ID: 11346368)
21. Pathological characterization of astrocytic hyaline inclusions in familial amyotrophic lateral sclerosis.
Kato S; Hayashi H; Nakashima K; Nanba E; Kato M; Hirano A; Nakano I; Asayama K; Ohama E
Am J Pathol; 1997 Aug; 151(2):611-20. PubMed ID: 9273821
[TBL] [Abstract][Full Text] [Related]
22. FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis.
Blair IP; Williams KL; Warraich ST; Durnall JC; Thoeng AD; Manavis J; Blumbergs PC; Vucic S; Kiernan MC; Nicholson GA
J Neurol Neurosurg Psychiatry; 2010 Jun; 81(6):639-45. PubMed ID: 19965854
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. Colocalization of 14-3-3 proteins with SOD1 in Lewy body-like hyaline inclusions in familial amyotrophic lateral sclerosis cases and the animal model.
Okamoto Y; Shirakashi Y; Ihara M; Urushitani M; Oono M; Kawamoto Y; Yamashita H; Shimohama S; Kato S; Hirano A; Tomimoto H; Ito H; Takahashi R
PLoS One; 2011; 6(5):e20427. PubMed ID: 21655264
[TBL] [Abstract][Full Text] [Related]
26. Familial amyotrophic lateral sclerosis. Molecular pathology of a patient with a SOD1 mutation.
Shaw CE; Enayat ZE; Powell JF; Anderson VE; Radunovic A; al-Sarraj S; Leigh PN
Neurology; 1997 Dec; 49(6):1612-6. PubMed ID: 9409355
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. Formation of advanced glycation end-product-modified superoxide dismutase-1 (SOD1) is one of the mechanisms responsible for inclusions common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutation, and transgenic mice expressing human SOD1 gene mutation.
Kato S; Nakashima K; Horiuchi S; Nagai R; Cleveland DW; Liu J; Hirano A; Takikawa M; Kato M; Nakano I; Sakoda S; Asayama K; Ohama E
Neuropathology; 2001 Mar; 21(1):67-81. PubMed ID: 11304045
[TBL] [Abstract][Full Text] [Related]
30. A novel SOD1 gene mutation in a Korean family with amyotrophic lateral sclerosis.
Kim NH; Kim HJ; Kim M; Lee KW
J Neurol Sci; 2003 Jan; 206(1):65-9. PubMed ID: 12480087
[TBL] [Abstract][Full Text] [Related]
31. Familial amyotrophic lateral sclerosis with Gly93Ser mutation in Cu/Zn superoxide dismutase: a clinical and neuropathological study.
Suzuki M; Irie T; Watanabe T; Mikami H; Yamazaki T; Oyanagi K; Ono S
J Neurol Sci; 2008 May; 268(1-2):140-4. PubMed ID: 18191946
[TBL] [Abstract][Full Text] [Related]
32. Inverse correlation between the formation of mitochondria-derived vacuoles and Lewy-body-like hyaline inclusions in G93A superoxide-dismutase-transgenic mice.
Sumi H; Nagano S; Fujimura H; Kato S; Sakoda S
Acta Neuropathol; 2006 Jul; 112(1):52-63. PubMed ID: 16642310
[TBL] [Abstract][Full Text] [Related]
33. FALS with Gly72Ser mutation in SOD1 gene: report of a family including the first autopsy case.
Kobayashi Z; Tsuchiya K; Kubodera T; Shibata N; Arai T; Miura H; Ishikawa C; Kondo H; Ishizu H; Akiyama H; Mizusawa H
J Neurol Sci; 2011 Jan; 300(1-2):9-13. PubMed ID: 21084099
[TBL] [Abstract][Full Text] [Related]
34. [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]
35. [Clinical features and neuropathological findings of familial amyotrophic lateral sclerosis with an H43R mutation in Cu/Zn superoxide dismutase].
Mochizuki Y; Mizutani T; Nakano R; Fukushima T; Honma T; Nemoto N; Takei K
Rinsho Shinkeigaku; 2003 Aug; 43(8):491-5. PubMed ID: 14658402
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.
Mackenzie IR; Bigio EH; Ince PG; Geser F; Neumann M; Cairns NJ; Kwong LK; Forman MS; Ravits J; Stewart H; Eisen A; McClusky L; Kretzschmar HA; Monoranu CM; Highley JR; Kirby J; Siddique T; Shaw PJ; Lee VM; Trojanowski JQ
Ann Neurol; 2007 May; 61(5):427-34. PubMed ID: 17469116
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Identification of a novel missense (C7W) mutation of SOD1 in a large familial amyotrophic lateral sclerosis pedigree.
Wang Z; Cai W; Cui F; Cai T; Chen Z; Mao F; Teng H; Chen L; Wang J; Sun Z; Huang X; Yu P
Neurobiol Aging; 2014 Mar; 35(3):725.e11-5. PubMed ID: 24094577
[TBL] [Abstract][Full Text] [Related]
40. Familial amyotrophic lateral sclerosis with widespread vacuolation and hyaline inclusions.
Sasaki S; Ohsawa Y; Yamane K; Sakuma H; Shibata N; Nakano R; Kikugawa K; Mizutani T; Tsuji S; Iwata M
Neurology; 1998 Sep; 51(3):871-3. PubMed ID: 9748044
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
