PAPER Tateishi T, Hokonohara T, Yamasaki R, Miura S, Kikuchi H, Iwaki A, Tashiro H, Furuya H, Nagara Y, Ohyagi Y, Nukina N, Iwaki T, Fukumaki Y, Kira J
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PAPER Damme PV, Goris A, Race V, Hersmus N, Dubois B, Bosch LV, Matthijs G, Robberecht W
The occurrence of mutations in FUS in a Belgian cohort of patients with familial ALS.
Eur J Neurol. 2010 May;17(5):754-6. Epub 2009 Nov 13 PubMed: 19922450PAPER Belzil VV, St-Onge J, Daoud H, Desjarlais A, Bouchard JP, Dupré N, Camu W, Dion PA, Rouleau GA
Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis.
J Hum Genet. 2011 Mar;56(3):247-9. Epub 2010 Dec 16 PubMed: 21160488PAPER Chiò A, Restagno G, Brunetti M, Ossola I, Calvo A, Mora G, Sabatelli M, Monsurrò MR, Battistini S, Mandrioli J, Salvi F, Spataro R, Schymick J, Traynor BJ, La Bella V, ITALSGEN Consortium
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation.
Neurobiol Aging. 2009 Aug;30(8):1272-5. Epub 2009 May 17 PubMed: 19450904PAPER Syriani E, Morales M, Gamez J
FUS/TLS gene mutations are the second most frequent cause of familial ALS in the Spanish population.
Amyotroph Lateral Scler. 2011 Mar;12(2):118-23. Epub 2010 Dec 6 PubMed: 21128870PAPER Nagayama S, Minato-Hashiba N, Nakata M, Kaito M, Nakanishi M, Tanaka K, Arai M, Akiyama H, Matsui M
Novel FUS mutation in patients with sporadic amyotrophic lateral sclerosis and corticobasal degeneration.
J Clin Neurosci. 2012 Dec;19(12):1738-9. Epub 2012 Sep 19 PubMed: 22999566PAPER Kwon MJ, Baek W, Ki CS, Kim HY, Koh SH, Kim JW, Kim SH
Screening of the SOD1, FUS, TARDBP, ANG, and OPTN mutations in Korean patients with familial and sporadic ALS.
Neurobiol Aging. 2012 May;33(5):1017.e17-23. Epub 2012 Jan 15 PubMed: 22244934PAPER Zou ZY, Peng Y, Feng XH, Wang XN, Sun Q, Liu MS, Li XG, Cui LY
Screening of the FUS gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin.
Eur J Neurol. 2012 Jul;19(7):977-83. Epub 2012 Feb 16 PubMed: 22340366PAPER Corrado L, Del Bo R, Castellotti B, Ratti A, Cereda C, Penco S, Sorarù G, Carlomagno Y, Ghezzi S, Pensato V, Colombrita C, Gagliardi S, Cozzi L, Orsetti V, Mancuso M, Siciliano G, Mazzini L, Comi GP, Gellera C, Ceroni M, D'Alfonso S, Silani V
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis.
J Med Genet. 2010 Mar;47(3):190-4. Epub 2009 Oct 26 PubMed: 19861302PAPER Belzil VV, Valdmanis PN, Dion PA, Daoud H, Kabashi E, Noreau A, Gauthier J, S2D team, Hince P, Desjarlais A, Bouchard JP, Lacomblez L, Salachas F, Pradat PF, Camu W, Meininger V, Dupré N, Rouleau GA
Mutations in FUS cause FALS and SALS in French and French Canadian populations.
Neurology. 2009 Oct 13;73(15):1176-9. Epub 2009 Sep 9 PubMed: 19741216PAPER Brown JA, Min J, Staropoli JF, Collin E, Bi S, Feng X, Barone R, Cao Y, O'Malley L, Xin W, Mullen TE, Sims KB
SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: a United States clinical testing lab experience.
Amyotroph Lateral Scler. 2012 Feb;13(2):217-22. PubMed: 22292843PAPER Belzil VV, Daoud H, St-Onge J, Desjarlais A, Bouchard JP, Dupre N, Lacomblez L, Salachas F, Pradat PF, Meininger V, Camu W, Dion PA, Rouleau GA
Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosis.
Amyotroph Lateral Scler. 2011 Mar;12(2):113-7. Epub 2011 Jan 24 PubMed: 21261515PAPER van Blitterswijk M, Vlam L, van Es MA, van der Pol WL, Hennekam EA, Dooijes D, Schelhaas HJ, van der Kooi AJ, de Visser M, Veldink JH, van den Berg LH
Genetic overlap between apparently sporadic motor neuron diseases.
PLoS One. 2012;7(11):e48983. Epub 2012 Nov 14 PubMed: 23155438Eva Hajos-Korcsok
Pfizer Inc.Cambridge, United States
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Other Alzheimer A. Über eine eigenartige Erkrankung der Hirnrinde Allgemeine Zeitschrift fur Psychiatrie und Psychisch-gerichtliche Medizin. 1907 Jan ; 64():146-8. ABSTRACT Click here to go back to the original German abstract. English translation: The
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