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Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1992 | 1 |
2006 | 1 |
2009 | 1 |
2010 | 1 |
2011 | 1 |
2012 | 2 |
2014 | 1 |
2024 | 0 |
PubMed (cited) for id: 612954
7 results
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Page 1
Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies.
Orphanet J Rare Dis. 2014 Aug 1;9:121. doi: 10.1186/s13023-014-0121-9.
Orphanet J Rare Dis. 2014.
PMID: 25208129
Free PMC article.
BAG3 mutations: another cause of giant axonal neuropathy.
Jaffer F, Murphy SM, Scoto M, Healy E, Rossor AM, Brandner S, Phadke R, Selcen D, Jungbluth H, Muntoni F, Reilly MM.
Jaffer F, et al.
J Peripher Nerv Syst. 2012 Jun;17(2):210-6. doi: 10.1111/j.1529-8027.2012.00409.x.
J Peripher Nerv Syst. 2012.
PMID: 22734908
Item in Clipboard
BAG3-related myofibrillar myopathy in a Chinese family.
Lee HC, Cherk SW, Chan SK, Wong S, Tong TW, Ho WS, Chan AY, Lee KC, Mak CM.
Lee HC, et al.
Clin Genet. 2012 Apr;81(4):394-8. doi: 10.1111/j.1399-0004.2011.01659.x. Epub 2011 Apr 4.
Clin Genet. 2012.
PMID: 21361913
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Inheritance patterns and phenotypic features of myofibrillar myopathy associated with a BAG3 mutation.
Odgerel Z, Sarkozy A, Lee HS, McKenna C, Rankin J, Straub V, Lochmüller H, Paola F, D'Amico A, Bertini E, Bushby K, Goldfarb LG.
Odgerel Z, et al.
Neuromuscul Disord. 2010 Jul;20(7):438-42. doi: 10.1016/j.nmd.2010.05.004. Epub 2010 Jun 3.
Neuromuscul Disord. 2010.
PMID: 20605452
Free PMC article.
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Mutation in BAG3 causes severe dominant childhood muscular dystrophy.
Selcen D, Muntoni F, Burton BK, Pegoraro E, Sewry C, Bite AV, Engel AG.
Selcen D, et al.
Ann Neurol. 2009 Jan;65(1):83-9. doi: 10.1002/ana.21553.
Ann Neurol. 2009.
PMID: 19085932
Free PMC article.
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BAG3 deficiency results in fulminant myopathy and early lethality.
Homma S, Iwasaki M, Shelton GD, Engvall E, Reed JC, Takayama S.
Homma S, et al.
Am J Pathol. 2006 Sep;169(3):761-73. doi: 10.2353/ajpath.2006.060250.
Am J Pathol. 2006.
PMID: 16936253
Free PMC article.
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Peripheral neuropathy with giant axons and cardiomyopathy associated with desmin type intermediate filaments in skeletal muscle.
Sabatelli M, Bertini E, Ricci E, Salviati G, Magi S, Papacci M, Tonali P.
Sabatelli M, et al.
J Neurol Sci. 1992 May;109(1):1-10. doi: 10.1016/0022-510x(92)90086-z.
J Neurol Sci. 1992.
PMID: 1517757
Review.
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