117 related articles for article (PubMed ID: 19726402)
1. Upregulation of persistent sodium conductances in familial ALS.
Vucic S; Kiernan MC
J Neurol Neurosurg Psychiatry; 2010 Feb; 81(2):222-7. PubMed ID: 19726402
[TBL] [Abstract][Full Text] [Related]
2. Axonal ion channel dysfunction in c9orf72 familial amyotrophic lateral sclerosis.
Geevasinga N; Menon P; Howells J; Nicholson GA; Kiernan MC; Vucic S
JAMA Neurol; 2015 Jan; 72(1):49-57. PubMed ID: 25384182
[TBL] [Abstract][Full Text] [Related]
3. Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis.
Vucic S; Nicholson GA; Kiernan MC
Brain; 2008 Jun; 131(Pt 6):1540-50. PubMed ID: 18469020
[TBL] [Abstract][Full Text] [Related]
4. Cortical Function in Asymptomatic Carriers and Patients With C9orf72 Amyotrophic Lateral Sclerosis.
Geevasinga N; Menon P; Nicholson GA; Ng K; Howells J; Kril JJ; Yiannikas C; Kiernan MC; Vucic S
JAMA Neurol; 2015 Nov; 72(11):1268-74. PubMed ID: 26348842
[TBL] [Abstract][Full Text] [Related]
5. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes.
Millecamps S; Boillée S; Le Ber I; Seilhean D; Teyssou E; Giraudeau M; Moigneu C; Vandenberghe N; Danel-Brunaud V; Corcia P; Pradat PF; Le Forestier N; Lacomblez L; Bruneteau G; Camu W; Brice A; Cazeneuve C; Leguern E; Meininger V; Salachas F
J Med Genet; 2012 Apr; 49(4):258-63. PubMed ID: 22499346
[TBL] [Abstract][Full Text] [Related]
6. Axonal excitability properties in amyotrophic lateral sclerosis.
Vucic S; Kiernan MC
Clin Neurophysiol; 2006 Jul; 117(7):1458-66. PubMed ID: 16759905
[TBL] [Abstract][Full Text] [Related]
7. Altered axonal excitability properties in amyotrophic lateral sclerosis: impaired potassium channel function related to disease stage.
Kanai K; Kuwabara S; Misawa S; Tamura N; Ogawara K; Nakata M; Sawai S; Hattori T; Bostock H
Brain; 2006 Apr; 129(Pt 4):953-62. PubMed ID: 16467388
[TBL] [Abstract][Full Text] [Related]
8. Alterations in anti-oxidative defence enzymes in erythrocytes from sporadic amyotrophic lateral sclerosis (SALS) and familial ALS patients.
Nikolić-Kokić A; Stević Z; Blagojević D; Davidović B; Jones DR; Spasić MB
Clin Chem Lab Med; 2006; 44(5):589-93. PubMed ID: 16681429
[TBL] [Abstract][Full Text] [Related]
9. Axonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral Sclerosis.
Iwai Y; Shibuya K; Misawa S; Sekiguchi Y; Watanabe K; Amino H; Kuwabara S
PLoS One; 2016; 11(7):e0158596. PubMed ID: 27383069
[TBL] [Abstract][Full Text] [Related]
10. Expression of hepatocyte growth factor and c-Met in the anterior horn cells of the spinal cord in the patients with amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS and familial ALS with superoxide dismutase 1 gene mutation.
Kato S; Funakoshi H; Nakamura T; Kato M; Nakano I; Hirano A; Ohama E
Acta Neuropathol; 2003 Aug; 106(2):112-20. PubMed ID: 12707786
[TBL] [Abstract][Full Text] [Related]
11. High metabolic level in patients with familial amyotrophic lateral sclerosis.
Funalot B; Desport JC; Sturtz F; Camu W; Couratier P
Amyotroph Lateral Scler; 2009 Apr; 10(2):113-7. PubMed ID: 18792852
[TBL] [Abstract][Full Text] [Related]
12. TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation.
Tan CF; Eguchi H; Tagawa A; Onodera O; Iwasaki T; Tsujino A; Nishizawa M; Kakita A; Takahashi H
Acta Neuropathol; 2007 May; 113(5):535-42. PubMed ID: 17333220
[TBL] [Abstract][Full Text] [Related]
13. Kinesin expression in the central nervous system of humans and transgenic hSOD1G93A mice with amyotrophic lateral sclerosis.
Kuźma-Kozakiewicz M; Chudy A; Gajewska B; Dziewulska D; Usarek E; Barańczyk-Kuźma A
Neurodegener Dis; 2013; 12(2):71-80. PubMed ID: 23006449
[TBL] [Abstract][Full Text] [Related]
14. Phosphorylated Smad2/3 immunoreactivity in sporadic and familial amyotrophic lateral sclerosis and its mouse model.
Nakamura M; Ito H; Wate R; Nakano S; Hirano A; Kusaka H
Acta Neuropathol; 2008 Mar; 115(3):327-34. PubMed ID: 18210139
[TBL] [Abstract][Full Text] [Related]
15. Characterization of human sporadic ALS biomarkers in the familial ALS transgenic mSOD1(G93A) mouse model.
Lilo E; Wald-Altman S; Solmesky LJ; Ben Yaakov K; Gershoni-Emek N; Bulvik S; Kassis I; Karussis D; Perlson E; Weil M
Hum Mol Genet; 2013 Dec; 22(23):4720-5. PubMed ID: 23836781
[TBL] [Abstract][Full Text] [Related]
16. Markedly reduced axonal potassium channel expression in human sporadic amyotrophic lateral sclerosis: an immunohistochemical study.
Shibuya K; Misawa S; Arai K; Nakata M; Kanai K; Yoshiyama Y; Ito K; Isose S; Noto Y; Nasu S; Sekiguchi Y; Fujimaki Y; Ohmori S; Kitamura H; Sato Y; Kuwabara S
Exp Neurol; 2011 Dec; 232(2):149-53. PubMed ID: 21906595
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Galectin-1 deficiency improves axonal swelling of motor neurones in SOD1(G93A) transgenic mice.
Kobayakawa Y; Sakumi K; Kajitani K; Kadoya T; Horie H; Kira J; Nakabeppu Y
Neuropathol Appl Neurobiol; 2015 Feb; 41(2):227-44. PubMed ID: 24707896
[TBL] [Abstract][Full Text] [Related]
19. Molecular basis of amyotrophic lateral sclerosis.
Liscic RM; Breljak D
Prog Neuropsychopharmacol Biol Psychiatry; 2011 Mar; 35(2):370-2. PubMed ID: 20655970
[TBL] [Abstract][Full Text] [Related]
20. Abnormalities in cortical and peripheral excitability in flail arm variant amyotrophic lateral sclerosis.
Vucic S; Kiernan MC
J Neurol Neurosurg Psychiatry; 2007 Aug; 78(8):849-52. PubMed ID: 17210625
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
