156 related articles for article (PubMed ID: 22980027)
1. Familial ALS with FUS P525L mutation: two Japanese sisters with multiple systems involvement.
Mochizuki Y; Isozaki E; Takao M; Hashimoto T; Shibuya M; Arai M; Hosokawa M; Kawata A; Oyanagi K; Mihara B; Mizutani T
J Neurol Sci; 2012 Dec; 323(1-2):85-92. PubMed ID: 22980027
[TBL] [Abstract][Full Text] [Related]
2. A Japanese patient with familial ALS and a p.K510M mutation in the gene for FUS (FUS) resulting in the totally locked-in state.
Mochizuki Y; Kawata A; Maruyama H; Homma T; Watabe K; Kawakami H; Komori T; Mizutani T; Matsubara S
Neuropathology; 2014 Oct; 34(5):504-9. PubMed ID: 24841222
[TBL] [Abstract][Full Text] [Related]
3. Multiple system degeneration with basophilic inclusions in Japanese ALS patients with FUS mutation.
Tateishi T; Hokonohara T; Yamasaki R; Miura S; Kikuchi H; Iwaki A; Tashiro H; Furuya H; Nagara Y; Ohyagi Y; Nukina N; Iwaki T; Fukumaki Y; Kira J
Acta Neuropathol; 2010 Mar; 119(3):355-64. PubMed ID: 19967541
[TBL] [Abstract][Full Text] [Related]
4. An autopsied case of sporadic adult-onset amyotrophic lateral sclerosis with FUS-positive basophilic inclusions.
Matsuoka T; Fujii N; Kondo A; Iwaki A; Hokonohara T; Honda H; Sasaki K; Suzuki SO; Iwaki T
Neuropathology; 2011 Feb; 31(1):71-6. PubMed ID: 20573033
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Occurrence of basophilic inclusions and FUS-immunoreactive neuronal and glial inclusions in a case of familial amyotrophic lateral sclerosis.
Kobayashi Z; Tsuchiya K; Arai T; Aoki M; Hasegawa M; Ishizu H; Akiyama H; Mizusawa H
J Neurol Sci; 2010 Jun; 293(1-2):6-11. PubMed ID: 20409561
[TBL] [Abstract][Full Text] [Related]
7. A Japanese ALS6 family with mutation R521C in the FUS/TLS gene: a clinical, pathological and genetic report.
Yamamoto-Watanabe Y; Watanabe M; Okamoto K; Fujita Y; Jackson M; Ikeda M; Nakazato Y; Ikeda Y; Matsubara E; Kawarabayashi T; Shoji M
J Neurol Sci; 2010 Sep; 296(1-2):59-63. PubMed ID: 20621307
[TBL] [Abstract][Full Text] [Related]
8. A clinical and pathological study of a Japanese case of Amyotrophic Lateral Sclerosis/Parkinsonism-Dementia Complex with family history.
Konagaya M; Kato T; Sakai M; Kuru S; Matsuoka Y; Konagaya Y; Hashizume Y; Tabira T
J Neurol; 2003 Feb; 250(2):164-70. PubMed ID: 12574946
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation.
Mackenzie IR; Ansorge O; Strong M; Bilbao J; Zinman L; Ang LC; Baker M; Stewart H; Eisen A; Rademakers R; Neumann M
Acta Neuropathol; 2011 Jul; 122(1):87-98. PubMed ID: 21604077
[TBL] [Abstract][Full Text] [Related]
11. [A 49-year-old man with progressive bulbar palsy and respiratory failure].
Motoi Y; Satoh K; Matsumine H; Wakiya M; Mori H; Shirai T; Kondo T; Mizuno Y
No To Shinkei; 1998 Jan; 50(1):93-100. PubMed ID: 9493205
[TBL] [Abstract][Full Text] [Related]
12. Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6.
Vance C; Rogelj B; Hortobágyi T; De Vos KJ; Nishimura AL; Sreedharan J; Hu X; Smith B; Ruddy D; Wright P; Ganesalingam J; Williams KL; Tripathi V; Al-Saraj S; Al-Chalabi A; Leigh PN; Blair IP; Nicholson G; de Belleroche J; Gallo JM; Miller CC; Shaw CE
Science; 2009 Feb; 323(5918):1208-1211. PubMed ID: 19251628
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosis.
Broustal O; Camuzat A; Guillot-Noël L; Guy N; Millecamps S; Deffond D; Lacomblez L; Golfier V; Hannequin D; Salachas F; Camu W; Didic M; Dubois B; Meininger V; Le Ber I; Brice A;
J Alzheimers Dis; 2010; 22(3):765-9. PubMed ID: 21158017
[TBL] [Abstract][Full Text] [Related]
15. FUS pathology in basophilic inclusion body disease.
Munoz DG; Neumann M; Kusaka H; Yokota O; Ishihara K; Terada S; Kuroda S; Mackenzie IR
Acta Neuropathol; 2009 Nov; 118(5):617-27. PubMed ID: 19830439
[TBL] [Abstract][Full Text] [Related]
16. [Amyotrophic lateral sclerosis (ALS) with the mutations in the fused in sarcoma/translocated in liposarcoma gene].
Aoki M
Rinsho Shinkeigaku; 2013; 53(11):1080-3. PubMed ID: 24291885
[TBL] [Abstract][Full Text] [Related]
17. [An autopsied case of dominantly affecting upper motor neuron with atrophy of the frontal and temporal lobes--with special reference to primary lateral sclerosis].
Konagaya M; Sakai M; Iida M; Hashizume Y
Rinsho Shinkeigaku; 1995 Apr; 35(4):384-90. PubMed ID: 7614764
[TBL] [Abstract][Full Text] [Related]
18. Transportin 1 accumulates in FUS inclusions in adult-onset ALS without FUS mutation.
Takeuchi R; Toyoshima Y; Tada M; Shiga A; Tanaka H; Shimohata M; Kimura K; Morita T; Kakita A; Nishizawa M; Takahashi H
Neuropathol Appl Neurobiol; 2013 Aug; 39(5):580-4. PubMed ID: 23362988
[No Abstract] [Full Text] [Related]
19. Deficient RNA-editing enzyme ADAR2 in an amyotrophic lateral sclerosis patient with a FUS(P525L) mutation.
Aizawa H; Hideyama T; Yamashita T; Kimura T; Suzuki N; Aoki M; Kwak S
J Clin Neurosci; 2016 Oct; 32():128-9. PubMed ID: 27343041
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]