714 related articles for article (PubMed ID: 21989245)
1. Clinical genetics of amyotrophic lateral sclerosis: what do we really know?
Andersen PM; Al-Chalabi A
Nat Rev Neurol; 2011 Oct; 7(11):603-15. PubMed ID: 21989245
[TBL] [Abstract][Full Text] [Related]
2. Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China.
Hou L; Jiao B; Xiao T; Zhou L; Zhou Z; Du J; Yan X; Wang J; Tang B; Shen L
Sci Rep; 2016 Sep; 6():32478. PubMed ID: 27604643
[TBL] [Abstract][Full Text] [Related]
3. FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis.
Blair IP; Williams KL; Warraich ST; Durnall JC; Thoeng AD; Manavis J; Blumbergs PC; Vucic S; Kiernan MC; Nicholson GA
J Neurol Neurosurg Psychiatry; 2010 Jun; 81(6):639-45. PubMed ID: 19965854
[TBL] [Abstract][Full Text] [Related]
4. [What is the role of the genetic survey in amyotrophic lateral sclerosis?].
Camu W
Rev Neurol (Paris); 2006 Jun; 162 Spec No 2():4S91-4S95. PubMed ID: 17128094
[TBL] [Abstract][Full Text] [Related]
5. De novo FUS gene mutations are associated with juvenile-onset sporadic amyotrophic lateral sclerosis in China.
Zou ZY; Cui LY; Sun Q; Li XG; Liu MS; Xu Y; Zhou Y; Yang XZ
Neurobiol Aging; 2013 Apr; 34(4):1312.e1-8. PubMed ID: 23046859
[TBL] [Abstract][Full Text] [Related]
6. Pathogenic Genome Signatures That Damage Motor Neurons in Amyotrophic Lateral Sclerosis.
Yousefian-Jazi A; Seol Y; Kim J; Ryu HL; Lee J; Ryu H
Cells; 2020 Dec; 9(12):. PubMed ID: 33333804
[TBL] [Abstract][Full Text] [Related]
7. TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations.
Del Bo R; Ghezzi S; Corti S; Pandolfo M; Ranieri M; Santoro D; Ghione I; Prelle A; Orsetti V; Mancuso M; Sorarù G; Briani C; Angelini C; Siciliano G; Bresolin N; Comi GP
Eur J Neurol; 2009 Jun; 16(6):727-32. PubMed ID: 19236453
[TBL] [Abstract][Full Text] [Related]
8. Pre-symptomatic diagnosis in ALS.
Corcia P; Lumbroso S; Cazeneuve C; Mouzat K; Camu W; Vourc'h P;
Rev Neurol (Paris); 2020 Mar; 176(3):166-169. PubMed ID: 31932031
[TBL] [Abstract][Full Text] [Related]
9. Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis.
Del Bo R; Tiloca C; Pensato V; Corrado L; Ratti A; Ticozzi N; Corti S; Castellotti B; Mazzini L; Sorarù G; Cereda C; D'Alfonso S; Gellera C; Comi GP; Silani V;
J Neurol Neurosurg Psychiatry; 2011 Nov; 82(11):1239-43. PubMed ID: 21613650
[TBL] [Abstract][Full Text] [Related]
10. [Genetics of amyotrophic lateral sclerosis].
Corcia P; Blasco H; Camu W
Presse Med; 2014 May; 43(5):555-62. PubMed ID: 24703222
[TBL] [Abstract][Full Text] [Related]
11. Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants.
Bertolin C; D'Ascenzo C; Querin G; Gaiani A; Boaretto F; Salvoro C; Vazza G; Angelini C; Cagnin A; Pegoraro E; Sorarù G; Mostacciuolo ML
Neurobiol Aging; 2014 May; 35(5):1212.e7-1212.e10. PubMed ID: 24325798
[TBL] [Abstract][Full Text] [Related]
12. Evidence for an oligogenic basis of amyotrophic lateral sclerosis.
van Blitterswijk M; van Es MA; Hennekam EA; Dooijes D; van Rheenen W; Medic J; Bourque PR; Schelhaas HJ; van der Kooi AJ; de Visser M; de Bakker PI; Veldink JH; van den Berg LH
Hum Mol Genet; 2012 Sep; 21(17):3776-84. PubMed ID: 22645277
[TBL] [Abstract][Full Text] [Related]
13. The genetics and neuropathology of amyotrophic lateral sclerosis.
Al-Chalabi A; Jones A; Troakes C; King A; Al-Sarraj S; van den Berg LH
Acta Neuropathol; 2012 Sep; 124(3):339-52. PubMed ID: 22903397
[TBL] [Abstract][Full Text] [Related]
14. Genetics of familial Amyotrophic lateral sclerosis.
Ticozzi N; Tiloca C; Morelli C; Colombrita C; Poletti B; Doretti A; Maderna L; Messina S; Ratti A; Silani V
Arch Ital Biol; 2011 Mar; 149(1):65-82. PubMed ID: 21412717
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Hereditary Amyotrophic Lateral Sclerosis. A report of two families.
Alter M; Schaumann B
Eur Neurol; 1976; 14(4):250-65. PubMed ID: 954772
[TBL] [Abstract][Full Text] [Related]
17. Emerging understanding of the genotype-phenotype relationship in amyotrophic lateral sclerosis.
Goutman SA; Chen KS; Paez-Colasante X; Feldman EL
Handb Clin Neurol; 2018; 148():603-623. PubMed ID: 29478603
[TBL] [Abstract][Full Text] [Related]
18. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.
Millecamps S; Salachas F; Cazeneuve C; Gordon P; Bricka B; Camuzat A; Guillot-Noël L; Russaouen O; Bruneteau G; Pradat PF; Le Forestier N; Vandenberghe N; Danel-Brunaud V; Guy N; Thauvin-Robinet C; Lacomblez L; Couratier P; Hannequin D; Seilhean D; Le Ber I; Corcia P; Camu W; Brice A; Rouleau G; LeGuern E; Meininger V
J Med Genet; 2010 Aug; 47(8):554-60. PubMed ID: 20577002
[TBL] [Abstract][Full Text] [Related]
19. FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis.
Deng HX; Zhai H; Bigio EH; Yan J; Fecto F; Ajroud K; Mishra M; Ajroud-Driss S; Heller S; Sufit R; Siddique N; Mugnaini E; Siddique T
Ann Neurol; 2010 Jun; 67(6):739-48. PubMed ID: 20517935
[TBL] [Abstract][Full Text] [Related]
20. Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis.
Stoccoro A; Smith AR; Mosca L; Marocchi A; Gerardi F; Lunetta C; Cereda C; Gagliardi S; Lunnon K; Migliore L; Coppedè F
Clin Epigenetics; 2020 Sep; 12(1):137. PubMed ID: 32917270
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]