145 related articles for article (PubMed ID: 16546761)
21. [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]
22. [Identification of the mutation of SOD1 gene in a familial amyotrophic lateral sclerosis].
Shi SG; Li LS; Chen KN; Liu X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):149-52. PubMed ID: 15079798
[TBL] [Abstract][Full Text] [Related]
23. Diffusion tensor imaging in sporadic and familial (D90A SOD1) forms of amyotrophic lateral sclerosis.
Stanton BR; Shinhmar D; Turner MR; Williams VC; Williams SC; Blain CR; Giampietro VP; Catani M; Leigh PN; Andersen PM; Simmons A
Arch Neurol; 2009 Jan; 66(1):109-15. PubMed ID: 19139308
[TBL] [Abstract][Full Text] [Related]
24. Molecular analysis of the superoxide dismutase 1 gene in Spanish patients with sporadic or familial amyotrophic lateral sclerosis.
García-Redondo A; Bustos F; Juan Y Seva B; Del Hoyo P; Jiménez S; Campos Y; Martín MA; Rubio JC; Cañadillas F; Arenas J; Esteban J
Muscle Nerve; 2002 Aug; 26(2):274-8. PubMed ID: 12210393
[TBL] [Abstract][Full Text] [Related]
25. N19S, a new SOD1 mutation in sporadic amyotrophic lateral sclerosis: no evidence for disease causation.
Mayeux V; Corcia P; Besson G; Jafari-Schluep HF; Briolotti V; Camu W
Ann Neurol; 2003 Jun; 53(6):815-8. PubMed ID: 12783432
[TBL] [Abstract][Full Text] [Related]
26. D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation.
Del Grande A; Conte A; Lattante S; Luigetti M; Marangi G; Zollino M; Madia F; Bisogni G; Sabatelli M
J Neurol Sci; 2011 Oct; 309(1-2):31-3. PubMed ID: 21839474
[TBL] [Abstract][Full Text] [Related]
27. "True" sporadic ALS associated with a novel SOD-1 mutation.
Alexander MD; Traynor BJ; Miller N; Corr B; Frost E; McQuaid S; Brett FM; Green A; Hardiman O
Ann Neurol; 2002 Nov; 52(5):680-3. PubMed ID: 12402272
[TBL] [Abstract][Full Text] [Related]
28. SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant.
Luigetti M; Lattante S; Zollino M; Conte A; Marangi G; Del Grande A; Sabatelli M
Neurobiol Aging; 2011 Oct; 32(10):1924.e15-8. PubMed ID: 21621297
[TBL] [Abstract][Full Text] [Related]
29. No association of the SOD1 locus and disease susceptibility or phenotype in sporadic ALS.
Broom WJ; Parton MJ; Vance CA; Russ C; Andersen PM; Hansen V; Leigh PN; Powell JF; Al-Chalabi A; Shaw CE
Neurology; 2004 Dec; 63(12):2419-22. PubMed ID: 15623718
[TBL] [Abstract][Full Text] [Related]
30. Novel SOD1 N86K mutation is associated with a severe phenotype in familial ALS.
Beck M; Sendtner M; Toyka KV
Muscle Nerve; 2007 Jul; 36(1):111-4. PubMed ID: 17299743
[TBL] [Abstract][Full Text] [Related]
31. Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotype.
Lunetta C; Sansone VA; Penco S; Mosca L; Tarlarini C; Avemaria F; Maestri E; Melazzini MG; Meola G; Corbo M
Eur J Neurol; 2014 Apr; 21(4):594-8. PubMed ID: 24471417
[TBL] [Abstract][Full Text] [Related]
32. Facial onset amyotrophic lateral sclerosis with K3E variant in the Cu/Zn superoxide dismutase gene.
Shibuya K; Sawai S; Sugiyama A; Koide M; Nishiyama A; Aoki M; Kuwabara S
Amyotroph Lateral Scler Frontotemporal Degener; 2021 Feb; 22(1-2):144-146. PubMed ID: 32729725
[TBL] [Abstract][Full Text] [Related]
33. Identify mutation in amyotrophic lateral sclerosis cases using HaloPlex target enrichment system.
Liu ZJ; Li HF; Tan GH; Tao QQ; Ni W; Cheng XW; Xiong ZQ; Wu ZY
Neurobiol Aging; 2014 Dec; 35(12):2881.e11-2881.e15. PubMed ID: 25109764
[TBL] [Abstract][Full Text] [Related]
34. Amyotrophic lateral sclerosis with mutation of the Cu/Zn superoxide dismutase gene (SOD1) in a patient with Down syndrome.
Marucci G; Morandi L; Bartolomei I; Salvi F; Pession A; Righi A; Lauria G; Foschini MP
Neuromuscul Disord; 2007 Oct; 17(9-10):673-6. PubMed ID: 17624778
[TBL] [Abstract][Full Text] [Related]
35. Genetics of amyotrophic lateral sclerosis.
Robberecht W
J Neurol; 2000 Dec; 247 Suppl 6():VI/2-6. PubMed ID: 19714405
[TBL] [Abstract][Full Text] [Related]
36. Amyotrophic lateral sclerosis as a complex genetic disease.
Simpson CL; Al-Chalabi A
Biochim Biophys Acta; 2006; 1762(11-12):973-85. PubMed ID: 16973338
[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. Red cell superoxide dismutase activity in sporadic amyotrophic lateral sclerosis.
Tuncel D; Aydin N; Aribal Kocatürk P; Ozelçi Kavas G; Sarikaya S
J Clin Neurosci; 2006 Dec; 13(10):991-4. PubMed ID: 17071091
[TBL] [Abstract][Full Text] [Related]
39. Genetics of amyotrophic lateral sclerosis.
Robberecht W
J Neurol; 2000 Dec; 247():2-6. PubMed ID: 11200702
[TBL] [Abstract][Full Text] [Related]
40. Heterozygous D90A-SOD1 mutation in a patient with facial onset sensory motor neuronopathy (FOSMN) syndrome: a bridge to amyotrophic lateral sclerosis.
Dalla Bella E; Rigamonti A; Mantero V; Morbin M; Saccucci S; Gellera C; Mora G; Lauria G
J Neurol Neurosurg Psychiatry; 2014 Sep; 85(9):1009-11. PubMed ID: 24591457
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
