81 related articles for article (PubMed ID: 11490451)
1. [Genetics of amyotrophic lateral sclerosis].
Andersen PM
Zh Nevrol Psikhiatr Im S S Korsakova; 2001; 101(3):54-63. PubMed ID: 11490451
[No Abstract] [Full Text] [Related]
2. Novel G16S (GGC-AGC) mutation in the SOD-1 gene in a patient with apparently sporadic young-onset amyotrophic lateral sclerosis.
Kawamata J; Shimohama S; Takano S; Harada K; Ueda K; Kimura J
Hum Mutat; 1997; 9(4):356-8. PubMed ID: 9101297
[No Abstract] [Full Text] [Related]
3. Proposed criteria for familial amyotrophic lateral sclerosis.
Byrne S; Bede P; Elamin M; Kenna K; Lynch C; McLaughlin R; Hardiman O
Amyotroph Lateral Scler; 2011 May; 12(3):157-9. PubMed ID: 21208036
[No Abstract] [Full Text] [Related]
4. Genotype-phenotype correlation in familial amyotrophic lateral sclerosis with SOD1 mutation.
Alimonti D; Malaspina A; Poloni TE; Ceroni M
Funct Neurol; 2000; 15(3):177-91. PubMed ID: 11062847
[No Abstract] [Full Text] [Related]
5. [Sporadic amyotrophic lateral sclerosis associated with Asp90Ala CuZn-superoxide dismutase mutations in Russia].
Skvortsova VI; Limborskaia SA; Slominskiĭ PA; Levitskaia NI; Levitskiĭ GN; Shadrina MI; Kondrat'eva EA
Zh Nevrol Psikhiatr Im S S Korsakova; 2000; 100(1):44-7. PubMed ID: 10666886
[TBL] [Abstract][Full Text] [Related]
6. A second ALS patient having an L67P mutation in exon 3 of the Cu/Zn superoxide dismutase gene.
Krieger C; Haase S; Scott P
Amyotroph Lateral Scler; 2011 Nov; 12(6):466-7. PubMed ID: 21692663
[No Abstract] [Full Text] [Related]
7. Superoxide dismutase, oxygen radical metabolism, and amyotrophic lateral sclerosis.
Patterson D; Warner HR; Fox LM; Rahmani Z
Mol Genet Med; 1994; 4():79-118. PubMed ID: 7981631
[No Abstract] [Full Text] [Related]
8. [Autosomal dominant ALS].
Abe K
Ryoikibetsu Shokogun Shirizu; 1999; (27 Pt 2):320-2. PubMed ID: 10434663
[No Abstract] [Full Text] [Related]
9. Familial amyotrophic lateral sclerosis/motor neurone disease (FALS): a review of current developments.
de Belleroche J; Orrell R; King A
J Med Genet; 1995 Nov; 32(11):841-7. PubMed ID: 8592323
[No Abstract] [Full Text] [Related]
10. Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosis.
Orrell RW; Habgood J; Rudge P; Lane RJ; de Belleroche JS
Ann Neurol; 1996 Jun; 39(6):810-2. PubMed ID: 8651656
[TBL] [Abstract][Full Text] [Related]
11. Cu/Zn superoxide dismutase gene mutations in amyotrophic lateral sclerosis: correlation between genotype and clinical features.
Laing NG; Siddique T
J Neurol Neurosurg Psychiatry; 1997 Dec; 63(6):815. PubMed ID: 9416831
[No Abstract] [Full Text] [Related]
12. 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]
13. Autosomal dominant amyotrophic lateral sclerosis: a novel mutation in the Cu/Zn superoxide dismutase-1 gene.
Kostrzewa M; Burck-Lehmann U; Müller U
Hum Mol Genet; 1994 Dec; 3(12):2261-2. PubMed ID: 7881433
[No Abstract] [Full Text] [Related]
14. Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers.
Rosen DR; Sapp P; O'Regan J; McKenna-Yasek D; Schlumpf KS; Haines JL; Gusella JF; Horvitz HR; Brown RH
Am J Med Genet; 1994 May; 51(1):61-9. PubMed ID: 7913294
[TBL] [Abstract][Full Text] [Related]
15. A shared chromosome-21 haplotype among amyotrophic lateral sclerosis families with the A4V SOD1 mutation.
Rosen DR
Clin Genet; 2004 Sep; 66(3):247-50. PubMed ID: 15324326
[No Abstract] [Full Text] [Related]
16. Leu106-->Val (CTC-->GTC) mutation of superoxide dismutase-1 gene in patient with familial amyotrophic lateral sclerosis in Japan.
Kawamata J; Hasegawa H; Shimohama S; Kimura J; Tanaka S; Ueda K
Lancet; 1994 Jun; 343(8911):1501. PubMed ID: 7911198
[No Abstract] [Full Text] [Related]
17. A specific superoxide dismutase mutation is on the same genetic background in sporadic and familial cases of amyotrophic lateral sclerosis.
Hayward C; Swingler RJ; Simpson SA; Brock DJ
Am J Hum Genet; 1996 Nov; 59(5):1165-7. PubMed ID: 8900247
[No Abstract] [Full Text] [Related]
18. [Free radicals as a cause of amyotrophic lateral sclerosis?].
Ignatius J
Duodecim; 1993; 109(12):1041-3. PubMed ID: 8062674
[No Abstract] [Full Text] [Related]
19. CuZnSOD-associated amyotrophic lateral sclerosis.
Radunović A; Shaw CE; Akman-Demir G; Idrisoglu H; Leigh PN
Ann Neurol; 1997 Aug; 42(2):273-4. PubMed ID: 9266745
[No Abstract] [Full Text] [Related]
20. Identification of a novel exon 4 SOD1 mutation in a sporadic amyotrophic lateral sclerosis patient.
Jones CT; Shaw PJ; Chari G; Brock DJ
Mol Cell Probes; 1994 Aug; 8(4):329-30. PubMed ID: 7870076
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]