205 related articles for article (PubMed ID: 22572540)
1. 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]
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. 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]
5. 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]
6. Screening of VCP mutations in Chinese amyotrophic lateral sclerosis patients.
Zou ZY; Liu MS; Li XG; Cui LY
Neurobiol Aging; 2013 May; 34(5):1519.e3-4. PubMed ID: 23102936
[TBL] [Abstract][Full Text] [Related]
7. 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]
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. VCP gene analyses in Japanese patients with sporadic amyotrophic lateral sclerosis identify a new mutation.
Hirano M; Nakamura Y; Saigoh K; Sakamoto H; Ueno S; Isono C; Mitsui Y; Kusunoki S
Neurobiol Aging; 2015 Mar; 36(3):1604.e1-6. PubMed ID: 25457024
[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. 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]
13. [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]
14. Novel p.Ile151Val mutation in VCP in a patient of African American descent with sporadic ALS.
DeJesus-Hernandez M; Desaro P; Johnston A; Ross OA; Wszolek ZK; Ertekin-Taner N; Graff-Radford NR; Rademakers R; Boylan K
Neurology; 2011 Sep; 77(11):1102-3. PubMed ID: 21880997
[No Abstract] [Full Text] [Related]
15. Mutations in FUS are the most frequent genetic cause in juvenile sporadic ALS patients of Chinese origin.
Zou ZY; Liu MS; Li XG; Cui LY
Amyotroph Lateral Scler Frontotemporal Degener; 2016; 17(3-4):249-52. PubMed ID: 26972116
[TBL] [Abstract][Full Text] [Related]
16. Pathogenic mutations in the ALS gene CCNF cause cytoplasmic mislocalization of Cyclin F and elevated VCP ATPase activity.
Yu Y; Nakagawa T; Morohoshi A; Nakagawa M; Ishida N; Suzuki N; Aoki M; Nakayama K
Hum Mol Genet; 2019 Oct; 28(20):3486-3497. PubMed ID: 31577344
[TBL] [Abstract][Full Text] [Related]
17. FUS mutations in sporadic amyotrophic lateral sclerosis.
Lai SL; Abramzon Y; Schymick JC; Stephan DA; Dunckley T; Dillman A; Cookson M; Calvo A; Battistini S; Giannini F; Caponnetto C; Mancardi GL; Spataro R; Monsurro MR; Tedeschi G; Marinou K; Sabatelli M; Conte A; Mandrioli J; Sola P; Salvi F; Bartolomei I; Lombardo F; ; Mora G; Restagno G; Chiò A; Traynor BJ
Neurobiol Aging; 2011 Mar; 32(3):550.e1-4. PubMed ID: 20138404
[TBL] [Abstract][Full Text] [Related]
18. Mutational analysis of the VCP gene in Parkinson's disease.
Majounie E; Traynor BJ; Chiò A; Restagno G; Mandrioli J; Benatar M; Taylor JP; Singleton AB
Neurobiol Aging; 2012 Jan; 33(1):209.e1-2. PubMed ID: 21920633
[TBL] [Abstract][Full Text] [Related]
19. Genetic analysis of VCP and WASH complex genes in a German cohort of sporadic ALS-FTD patients.
Türk M; Schröder R; Khuller K; Hofmann A; Berwanger C; Ludolph AC; Dekomien G; Müller K; Weishaupt JH; Thiel CT; Clemen CS
Neurobiol Aging; 2017 Aug; 56():213.e1-213.e5. PubMed ID: 28551275
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
