Similar articles for PMID: 14659406

Year	Number of Results
1996	1
1997	3
1998	2
1999	3
2000	1
2001	3
2002	3
2003	3
2004	8
2005	10
2006	4
2007	10
2008	7
2009	6
2010	7
2011	5
2012	2
2013	2
2015	1
2017	1
2018	3
2021	1
2022	2
2023	1
2024	0

1

Identification of a locus for an autosomal recessive hyaline body myopathy at chromosome 3p22.2-p21.32.

Onengüt S, Uğur SA, Karasoy H, Yüceyar N, Tolun A. Onengüt S, et al. Neuromuscul Disord. 2004 Jan;14(1):4-9. doi: 10.1016/s0960-8966(03)00163-9. Neuromuscul Disord. 2004. PMID: 14659406

2

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

3

Myosin storage (hyaline body) myopathy: a case report.

Shingde MV, Spring PJ, Maxwell A, Wills EJ, Harper CG, Dye DE, Laing NG, North KN. Shingde MV, et al. Neuromuscul Disord. 2006 Dec;16(12):882-6. doi: 10.1016/j.nmd.2006.09.001. Epub 2006 Nov 21. Neuromuscul Disord. 2006. PMID: 17118657

4

Hyaline body myopathy: adulthood manifestations.

Rafay MF, Halliday W, Bril V. Rafay MF, et al. Can J Neurol Sci. 2005 May;32(2):253-6. doi: 10.1017/s0317167100004078. Can J Neurol Sci. 2005. PMID: 16018165

5

Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy.

Bohlega S, Abu-Amero SN, Wakil SM, Carroll P, Al-Amr R, Lach B, Al-Sayed Y, Cupler EJ, Meyer BF. Bohlega S, et al. Neurology. 2004 May 11;62(9):1518-21. doi: 10.1212/01.wnl.0000123255.92062.37. Neurology. 2004. PMID: 15136674

6

Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy.

Oldfors A, Tajsharghi H, Thornell LE. Oldfors A, et al. Neurology. 2005 Feb 8;64(3):580-1; author reply 580-1. doi: 10.1212/wnl.64.3.580-a. Neurology. 2005. PMID: 15699411 Review. No abstract available.

7

Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophy.

Makri S, Clarke NF, Richard P, Maugenre S, Demay L, Bonne G, Guicheney P. Makri S, et al. Neuromuscul Disord. 2009 Jan;19(1):26-8. doi: 10.1016/j.nmd.2008.09.016. Epub 2008 Dec 11. Neuromuscul Disord. 2009. PMID: 19084400

8

New skeletal myopathy and cardiomyopathy associated with a missense mutation in MYH7.

Darin N, Tajsharghi H, Ostman-Smith I, Gilljam T, Oldfors A. Darin N, et al. Neurology. 2007 Jun 5;68(23):2041-2. doi: 10.1212/01.wnl.0000264430.55233.72. Neurology. 2007. PMID: 17548557 No abstract available.

9

Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene.

Jungbluth H, Zhou H, Hartley L, Halliger-Keller B, Messina S, Longman C, Brockington M, Robb SA, Straub V, Voit T, Swash M, Ferreiro A, Bydder G, Sewry CA, Müller C, Muntoni F. Jungbluth H, et al. Neurology. 2005 Dec 27;65(12):1930-5. doi: 10.1212/01.wnl.0000188870.37076.f2. Neurology. 2005. PMID: 16380615

10

Scoliosis surgery in a patient with "de novo" myosin storage myopathy.

Stalpers X, Verrips A, Braakhekke J, Lammens M, van den Wijngaard A, Mostert A. Stalpers X, et al. Neuromuscul Disord. 2011 Nov;21(11):812-5. doi: 10.1016/j.nmd.2011.05.005. Epub 2011 Jun 30. Neuromuscul Disord. 2011. PMID: 21723124

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