Cited Articles for PMCID: 3235861

Year	Number of Results
1996	2
1998	2
2004	3
2005	3
2007	2
2008	1
2009	4
2010	1
2011	1
2024	0

1

Selcen D. Selcen D. Neuromuscul Disord. 2011 Mar;21(3):161-71. doi: 10.1016/j.nmd.2010.12.007. Epub 2011 Jan 20. Neuromuscul Disord. 2011. PMID: 21256014 Free PMC article. Review.

2

The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathy.

Reilich P, Schoser B, Schramm N, Krause S, Schessl J, Kress W, Müller-Höcker J, Walter MC, Lochmuller H. Reilich P, et al. Neuromuscul Disord. 2010 Apr;20(4):255-9. doi: 10.1016/j.nmd.2010.01.012. Epub 2010 Feb 19. Neuromuscul Disord. 2010. PMID: 20171888

3

Extralysosomal protein degradation in myofibrillar myopathies.

Olivé M. Olivé M. Brain Pathol. 2009 Jul;19(3):507-15. doi: 10.1111/j.1750-3639.2009.00288.x. Brain Pathol. 2009. PMID: 19563542 Free PMC article. Review.

4

Myofibrillar myopathies: a clinical and myopathological guide.

Schröder R, Schoser B. Schröder R, et al. Brain Pathol. 2009 Jul;19(3):483-92. doi: 10.1111/j.1750-3639.2009.00289.x. Brain Pathol. 2009. PMID: 19563540 Free PMC article. Review.

5

Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study.

Claeys KG, van der Ven PF, Behin A, Stojkovic T, Eymard B, Dubourg O, Laforêt P, Faulkner G, Richard P, Vicart P, Romero NB, Stoltenburg G, Udd B, Fardeau M, Voit T, Fürst DO. Claeys KG, et al. Acta Neuropathol. 2009 Mar;117(3):293-307. doi: 10.1007/s00401-008-0479-7. Epub 2009 Jan 17. Acta Neuropathol. 2009. PMID: 19151983

6

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.

7

Molecular pathology of myofibrillar myopathies.

Ferrer I, Olivé M. Ferrer I, et al. Expert Rev Mol Med. 2008 Sep 3;10:e25. doi: 10.1017/S1462399408000793. Expert Rev Mol Med. 2008. PMID: 18764962 Review.

8

Conspicuous involvement of desmin tail mutations in diverse cardiac and skeletal myopathies.

Bär H, Goudeau B, Wälde S, Casteras-Simon M, Mücke N, Shatunov A, Goldberg YP, Clarke C, Holton JL, Eymard B, Katus HA, Fardeau M, Goldfarb L, Vicart P, Herrmann H. Bär H, et al. Hum Mutat. 2007 Apr;28(4):374-86. doi: 10.1002/humu.20459. Hum Mutat. 2007. PMID: 17221859

9

Absence of upregulated genes associated with protein accumulations in desmin myopathy.

Raju R, Dalakas MC. Raju R, et al. Muscle Nerve. 2007 Mar;35(3):386-8. doi: 10.1002/mus.20680. Muscle Nerve. 2007. PMID: 17068785

10

A mutation in myotilin causes spheroid body myopathy.

Foroud T, Pankratz N, Batchman AP, Pauciulo MW, Vidal R, Miravalle L, Goebel HH, Cushman LJ, Azzarelli B, Horak H, Farlow M, Nichols WC. Foroud T, et al. Neurology. 2005 Dec 27;65(12):1936-40. doi: 10.1212/01.wnl.0000188872.28149.9a. Neurology. 2005. PMID: 16380616

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