293 related articles for article (PubMed ID: 15235802)
1. 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]
2. 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]
3. [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]
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. 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]
6. 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]
7. 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]
8. Hoarseness due to bilateral vocal cord paralysis as an initial manifestation of familial amyotrophic lateral sclerosis.
Fukae J; Kubo S; Hattori N; Komatsu K; Kato M; Aoki M; Mizuno Y
Amyotroph Lateral Scler Other Motor Neuron Disord; 2005 Jun; 6(2):122-4. PubMed ID: 16036438
[TBL] [Abstract][Full Text] [Related]
9. [On intra-familial clinical diversities of a familial amyotrophic lateral sclerosis with a point mutation of Cu/Zn superoxide dismutase (Asn 86-Ser].
Maeda T; Kurahashi K; Matsunaga M; Inoue K; Inoue M
No To Shinkei; 1997 Sep; 49(9):847-51. PubMed ID: 9311004
[TBL] [Abstract][Full Text] [Related]
10. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.
Rosen DR; Siddique T; Patterson D; Figlewicz DA; Sapp P; Hentati A; Donaldson D; Goto J; O'Regan JP; Deng HX
Nature; 1993 Mar; 362(6415):59-62. PubMed ID: 8446170
[TBL] [Abstract][Full Text] [Related]
11. A novel exon 3 mutation (D76V) in the SOD1 gene associated with slowly progressive ALS.
Segovia-Silvestre T; Andreu AL; Vives-Bauza C; Garcia-Arumi E; Cervera C; Gamez J
Amyotroph Lateral Scler Other Motor Neuron Disord; 2002 Jun; 3(2):69-74. PubMed ID: 12215228
[TBL] [Abstract][Full Text] [Related]
12. SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis.
Rouleau GA; Clark AW; Rooke K; Pramatarova A; Krizus A; Suchowersky O; Julien JP; Figlewicz D
Ann Neurol; 1996 Jan; 39(1):128-31. PubMed ID: 8572658
[TBL] [Abstract][Full Text] [Related]
13. Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in Belgium.
Aguirre T; Matthijs G; Robberecht W; Tilkin P; Cassiman JJ
Eur J Hum Genet; 1999 Jul; 7(5):599-602. PubMed ID: 10439968
[TBL] [Abstract][Full Text] [Related]
14. Identification of two novel mutations in the Cu/Zn superoxide dismutase gene with familial amyotrophic lateral sclerosis: mass spectrometric and genomic analyses.
Sato T; Yamamoto Y; Nakanishi T; Fukada K; Sugai F; Zhou Z; Okuno T; Nagano S; Hirata S; Shimizu A; Sakoda S
J Neurol Sci; 2004 Mar; 218(1-2):79-83. PubMed ID: 14759637
[TBL] [Abstract][Full Text] [Related]
15. Identification of a novel D109Y mutation in Cu/Zn superoxide dismutase (sod1) gene associated with amyotrophic lateral sclerosis.
Naini A; Mehrazin M; Lu J; Gordon P; Mitsumoto H
J Neurol Sci; 2007 Mar; 254(1-2):17-21. PubMed ID: 17257622
[TBL] [Abstract][Full Text] [Related]
16. Variance of age at onset in a Japanese family with amyotrophic lateral sclerosis associated with a novel Cu/Zn superoxide dismutase mutation.
Aoki M; Abe K; Houi K; Ogasawara M; Matsubara Y; Kobayashi T; Mochio S; Narisawa K; Itoyama Y
Ann Neurol; 1995 May; 37(5):676-9. PubMed ID: 7755363
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Amyotrophic lateral sclerosis associated with genetic abnormalities in the gene encoding Cu/Zn superoxide dismutase: molecular pathology of five new cases, and comparison with previous reports and 73 sporadic cases of ALS.
Ince PG; Tomkins J; Slade JY; Thatcher NM; Shaw PJ
J Neuropathol Exp Neurol; 1998 Oct; 57(10):895-904. PubMed ID: 9786240
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]