188 related articles for article (PubMed ID: 8858006)
1. Familial amyotrophic lateral sclerosis with a two base pair deletion in superoxide dismutase 1: gene multisystem degeneration with intracytoplasmic hyaline inclusions in astrocytes.
Kato S; Shimoda M; Watanabe Y; Nakashima K; Takahashi K; Ohama E
J Neuropathol Exp Neurol; 1996 Oct; 55(10):1089-101. PubMed ID: 8858006
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Recent advances in research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutations: neuronal Lewy body-like hyaline inclusions and astrocytic hyaline inclusions.
Kato S; Saito M; Hirano A; Ohama E
Histol Histopathol; 1999 Jul; 14(3):973-89. PubMed ID: 10425565
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Familial amyotrophic lateral sclerosis with His46Arg mutation in Cu/Zn superoxide dismutase presenting characteristic clinical features and Lewy body-like hyaline inclusions.
Ohi T; Nabeshima K; Kato S; Yazawa S; Takechi S
J Neurol Sci; 2004 Oct; 225(1-2):19-25. PubMed ID: 15465081
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Astrocytic hyaline inclusions contain advanced glycation endproducts in familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutation: immunohistochemical and immunoelectron microscopical analyses.
Kato S; Horiuchi S; Nakashima K; Hirano A; Shibata N; Nakano I; Saito M; Kato M; Asayama K; Ohama E
Acta Neuropathol; 1999 Mar; 97(3):260-6. PubMed ID: 10090673
[TBL] [Abstract][Full Text] [Related]
10. [Familial amyotrophic lateral sclerosis and mutations in the Cu/Zn superoxide dismutase gene].
Nakano R
Rinsho Shinkeigaku; 1995 Dec; 35(12):1546-8. PubMed ID: 8752459
[TBL] [Abstract][Full Text] [Related]
11. Copper chaperone for superoxide dismutase co-aggregates with superoxide dismutase 1 (SOD1) in neuronal Lewy body-like hyaline inclusions: an immunohistochemical study on familial amyotrophic lateral sclerosis with SOD1 gene mutation.
Kato S; Sumi-Akamaru H; Fujimura H; Sakoda S; Kato M; Hirano A; Takikawa M; Ohama E
Acta Neuropathol; 2001 Sep; 102(3):233-8. PubMed ID: 11585247
[TBL] [Abstract][Full Text] [Related]
12. Familial amyotrophic lateral sclerosis with Cys111Tyr mutation in Cu/Zn superoxide dismutase showing widespread Lewy body-like hyaline inclusions.
Suzuki M; Yasui K; Ishikawai H; Nomura M; Watanabe T; Mikami H; Yamano T; Ono S
J Neurol Sci; 2011 Jan; 300(1-2):182-4. PubMed ID: 20888599
[TBL] [Abstract][Full Text] [Related]
13. [Two siblings of familial amyotrophic lateral sclerosis with multisystemic degeneration characterized by mild involvement of the middle root zone of the posterior column, Clarke's nuclei and spinocerebellar tract].
Yoshida M; Okuda S; Murakami N; Hashizume Y; Sobue G
Rinsho Shinkeigaku; 1995 Jun; 35(6):589-99. PubMed ID: 8521632
[TBL] [Abstract][Full Text] [Related]
14. A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset and incomplete penetrance in China.
Zhang H; Zhao H; Lu M; Zhang Y; Wang L; Zhang J; Ma D; Fan D
Amyotroph Lateral Scler Other Motor Neuron Disord; 2005 Dec; 6(4):234-8. PubMed ID: 16319027
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. [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]
18. Distinctive clinicopathological features of 2 large families with amyotrophic lateral sclerosis having L106V mutation in SOD1 gene.
Hineno A; Nakamura A; Shimojima Y; Yoshida K; Oyanagai K; Ikeda S
J Neurol Sci; 2012 Aug; 319(1-2):63-74. PubMed ID: 22647583
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
