334 related articles for article (PubMed ID: 25618255)
1. VCP mutations are not a major cause of familial amyotrophic lateral sclerosis in the UK.
Kwok CT; Wang HY; Morris AG; Smith B; Shaw C; de Belleroche J
J Neurol Sci; 2015 Feb; 349(1-2):209-13. PubMed ID: 25618255
[TBL] [Abstract][Full Text] [Related]
2. VCP mutations in familial and sporadic amyotrophic lateral sclerosis.
Koppers M; van Blitterswijk MM; Vlam L; Rowicka PA; van Vught PW; Groen EJ; Spliet WG; Engelen-Lee J; Schelhaas HJ; de Visser M; van der Kooi AJ; van der Pol WL; Pasterkamp RJ; Veldink JH; van den Berg LH
Neurobiol Aging; 2012 Apr; 33(4):837.e7-13. PubMed ID: 22078486
[TBL] [Abstract][Full Text] [Related]
3. Mutation analysis of VCP in familial and sporadic amyotrophic lateral sclerosis.
Williams KL; Solski JA; Nicholson GA; Blair IP
Neurobiol Aging; 2012 Jul; 33(7):1488.e15-6. PubMed ID: 22196955
[TBL] [Abstract][Full Text] [Related]
4. Immunoreactivity of valosin-containing protein in sporadic amyotrophic lateral sclerosis and in a case of its novel mutant.
Ayaki T; Ito H; Fukushima H; Inoue T; Kondo T; Ikemoto A; Asano T; Shodai A; Fujita T; Fukui S; Morino H; Nakano S; Kusaka H; Yamashita H; Ihara M; Matsumoto R; Kawamata J; Urushitani M; Kawakami H; Takahashi R
Acta Neuropathol Commun; 2014 Dec; 2():172. PubMed ID: 25492614
[TBL] [Abstract][Full Text] [Related]
5. Mutational analysis of VCP gene in familial amyotrophic lateral sclerosis.
Tiloca C; Ratti A; Pensato V; Castucci A; Sorarù G; Del Bo R; Corrado L; Cereda C; D'Ascenzo C; Comi GP; Mazzini L; Castellotti B; Ticozzi N; Gellera C; Silani V;
Neurobiol Aging; 2012 Mar; 33(3):630.e1-2. PubMed ID: 22137929
[TBL] [Abstract][Full Text] [Related]
6. Mutation analysis of VCP in British familial and sporadic amyotrophic lateral sclerosis patients.
Miller JW; Smith BN; Topp SD; Al-Chalabi A; Shaw CE; Vance C
Neurobiol Aging; 2012 Nov; 33(11):2721.e1-2. PubMed ID: 22789697
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. One family, one gene and three phenotypes: A novel VCP (valosin-containing protein) mutation associated with myopathy with rimmed vacuoles, amyotrophic lateral sclerosis and frontotemporal dementia.
Abrahao A; Abath Neto O; Kok F; Zanoteli E; Santos B; Pinto WB; Barsottini OG; Oliveira AS; Pedroso JL
J Neurol Sci; 2016 Sep; 368():352-8. PubMed ID: 27538664
[TBL] [Abstract][Full Text] [Related]
9. Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosis.
González-Pérez P; Cirulli ET; Drory VE; Dabby R; Nisipeanu P; Carasso RL; Sadeh M; Fox A; Festoff BW; Sapp PC; McKenna-Yasek D; Goldstein DB; Brown RH; Blumen SC
Neurology; 2012 Nov; 79(22):2201-8. PubMed ID: 23152587
[TBL] [Abstract][Full Text] [Related]
10. Frequency of C9orf72 hexanucleotide repeat expansion and SOD1 mutations in Portuguese patients with amyotrophic lateral sclerosis.
Gromicho M; Pinto S; Gisca E; Pronto-Laborinho AC; Andersen PM; de Carvalho M
Neurobiol Aging; 2018 Oct; 70():325.e7-325.e15. PubMed ID: 29861044
[TBL] [Abstract][Full Text] [Related]
11. Exome sequencing reveals VCP mutations as a cause of familial ALS.
Johnson JO; Mandrioli J; Benatar M; Abramzon Y; Van Deerlin VM; Trojanowski JQ; Gibbs JR; Brunetti M; Gronka S; Wuu J; Ding J; McCluskey L; Martinez-Lage M; Falcone D; Hernandez DG; Arepalli S; Chong S; Schymick JC; Rothstein J; Landi F; Wang YD; Calvo A; Mora G; Sabatelli M; Monsurrò MR; Battistini S; Salvi F; Spataro R; Sola P; Borghero G; ; Galassi G; Scholz SW; Taylor JP; Restagno G; Chiò A; Traynor BJ
Neuron; 2010 Dec; 68(5):857-64. PubMed ID: 21145000
[TBL] [Abstract][Full Text] [Related]
12. Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosis.
Abramzon Y; Johnson JO; Scholz SW; Taylor JP; Brunetti M; Calvo A; Mandrioli J; Benatar M; Mora G; Restagno G; Chiò A; Traynor BJ
Neurobiol Aging; 2012 Sep; 33(9):2231.e1-2231.e6. PubMed ID: 22572540
[TBL] [Abstract][Full Text] [Related]
13. The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis.
Nalbandian A; Donkervoort S; Dec E; Badadani M; Katheria V; Rana P; Nguyen C; Mukherjee J; Caiozzo V; Martin B; Watts GD; Vesa J; Smith C; Kimonis VE
J Mol Neurosci; 2011 Nov; 45(3):522-31. PubMed ID: 21892620
[TBL] [Abstract][Full Text] [Related]
14. Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases.
van Rheenen W; van Blitterswijk M; Huisman MH; Vlam L; van Doormaal PT; Seelen M; Medic J; Dooijes D; de Visser M; van der Kooi AJ; Raaphorst J; Schelhaas HJ; van der Pol WL; Veldink JH; van den Berg LH
Neurology; 2012 Aug; 79(9):878-82. PubMed ID: 22843265
[TBL] [Abstract][Full Text] [Related]
15. [A patient with familial amyotrophic lateral sclerosis associated with a new valosin-containing protein (VCP) gene mutation].
Segawa M; Hoshi A; Naruse H; Kuroda M; Bujo H; Ugawa Y
Rinsho Shinkeigaku; 2015; 55(12):914-20. PubMed ID: 26511028
[TBL] [Abstract][Full Text] [Related]
16. A hexanucleotide repeat expansion in C9ORF72 causes familial and sporadic ALS in Taiwan.
Tsai CP; Soong BW; Tu PH; Lin KP; Fuh JL; Tsai PC; Lu YC; Lee IH; Lee YC
Neurobiol Aging; 2012 Sep; 33(9):2232.e11-2232.e18. PubMed ID: 22673113
[TBL] [Abstract][Full Text] [Related]
17. Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis.
Fifita JA; Zhang KY; Galper J; Williams KL; McCann EP; Hogan AL; Saunders N; Bauer D; Tarr IS; Pamphlett R; Nicholson GA; Rowe D; Yang S; Blair IP
Neurodegener Dis; 2017; 17(6):304-312. PubMed ID: 29131108
[TBL] [Abstract][Full Text] [Related]
18. Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis.
Weihl CC; Baloh RH; Lee Y; Chou TF; Pittman SK; Lopate G; Allred P; Jockel-Balsarotti J; Pestronk A; Harms MB
Neuromuscul Disord; 2015 Apr; 25(4):289-96. PubMed ID: 25617006
[TBL] [Abstract][Full Text] [Related]
19. Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone.
Lucas GJ; Mehta SG; Hocking LJ; Stewart TL; Cundy T; Nicholson GC; Walsh JP; Fraser WD; Watts GD; Ralston SH; Kimonis VE
Bone; 2006 Feb; 38(2):280-5. PubMed ID: 16199218
[TBL] [Abstract][Full Text] [Related]
20. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.
Chiò A; Borghero G; Restagno G; Mora G; Drepper C; Traynor BJ; Sendtner M; Brunetti M; Ossola I; Calvo A; Pugliatti M; Sotgiu MA; Murru MR; Marrosu MG; Marrosu F; Marinou K; Mandrioli J; Sola P; Caponnetto C; Mancardi G; Mandich P; La Bella V; Spataro R; Conte A; Monsurrò MR; Tedeschi G; Pisano F; Bartolomei I; Salvi F; Lauria Pinter G; Simone I; Logroscino G; Gambardella A; Quattrone A; Lunetta C; Volanti P; Zollino M; Penco S; Battistini S; ; Renton AE; Majounie E; Abramzon Y; Conforti FL; Giannini F; Corbo M; Sabatelli M
Brain; 2012 Mar; 135(Pt 3):784-93. PubMed ID: 22366794
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]