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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 1 |
2012 | 1 |
2013 | 2 |
2014 | 1 |
2015 | 1 |
2024 | 0 |
PubMed (cited) for id: 616437
6 results
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Page 1
A phenotype of atypical apraxia of speech in a family carrying SQSTM1 mutation.
J Alzheimers Dis. 2015;43(2):625-30. doi: 10.3233/JAD-141512.
J Alzheimers Dis. 2015.
PMID: 25114083
Free PMC article.
SQSTM1 mutations--bridging Paget disease of bone and ALS/FTLD.
Rea SL, Majcher V, Searle MS, Layfield R.
Rea SL, et al.
Exp Cell Res. 2014 Jul 1;325(1):27-37. doi: 10.1016/j.yexcr.2014.01.020. Epub 2014 Jan 30.
Exp Cell Res. 2014.
PMID: 24486447
Review.
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SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis.
Le Ber I, Camuzat A, Guerreiro R, Bouya-Ahmed K, Bras J, Nicolas G, Gabelle A, Didic M, De Septenville A, Millecamps S, Lenglet T, Latouche M, Kabashi E, Campion D, Hannequin D, Hardy J, Brice A; French Clinical and Genetic Research Network on FTD/FTD-ALS.
Le Ber I, et al.
JAMA Neurol. 2013 Nov;70(11):1403-10. doi: 10.1001/jamaneurol.2013.3849.
JAMA Neurol. 2013.
PMID: 24042580
Free PMC article.
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Mutations in the gene encoding p62 in Japanese patients with amyotrophic lateral sclerosis.
Hirano M, Nakamura Y, Saigoh K, Sakamoto H, Ueno S, Isono C, Miyamoto K, Akamatsu M, Mitsui Y, Kusunoki S.
Hirano M, et al.
Neurology. 2013 Jan 29;80(5):458-63. doi: 10.1212/WNL.0b013e31827f0fe5. Epub 2013 Jan 9.
Neurology. 2013.
PMID: 23303844
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SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Rubino E, Rainero I, Chiò A, Rogaeva E, Galimberti D, Fenoglio P, Grinberg Y, Isaia G, Calvo A, Gentile S, Bruni AC, St George-Hyslop PH, Scarpini E, Gallone S, Pinessi L; TODEM Study Group.
Rubino E, et al.
Neurology. 2012 Oct 9;79(15):1556-62. doi: 10.1212/WNL.0b013e31826e25df. Epub 2012 Sep 12.
Neurology. 2012.
PMID: 22972638
Free PMC article.
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SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis.
Fecto F, Yan J, Vemula SP, Liu E, Yang Y, Chen W, Zheng JG, Shi Y, Siddique N, Arrat H, Donkervoort S, Ajroud-Driss S, Sufit RL, Heller SL, Deng HX, Siddique T.
Fecto F, et al.
Arch Neurol. 2011 Nov;68(11):1440-6. doi: 10.1001/archneurol.2011.250.
Arch Neurol. 2011.
PMID: 22084127
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