Similar articles for PMID: 19858127

Year	Number of Results
1976	1
1979	1
1981	1
1983	1
1994	1
1997	1
1998	3
1999	6
2000	2
2001	2
2002	1
2003	1
2004	5
2005	10
2006	4
2007	7
2008	4
2009	13
2010	11
2011	6
2012	5
2013	5
2014	6
2015	6
2016	5
2017	4
2018	6
2019	4
2020	3
2021	6
2022	6
2023	2
2024	0

1

Unexpected myopathy associated with a mutation in MYBPC3 and misplacement of the cardiac myosin binding protein C.

Tajsharghi H, Leren TP, Abdul-Hussein S, Tulinius M, Brunvand L, Dahl HM, Oldfors A. Tajsharghi H, et al. J Med Genet. 2010 Aug;47(8):575-7. doi: 10.1136/jmg.2009.072710. Epub 2009 Oct 26. J Med Genet. 2010. PMID: 19858127

2

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.

3

Homozygous mutation in MYH7 in myosin storage myopathy and cardiomyopathy.

Tajsharghi H, Oldfors A, Macleod DP, Swash M. Tajsharghi H, et al. Neurology. 2007 Mar 20;68(12):962. doi: 10.1212/01.wnl.0000257131.13438.2c. Neurology. 2007. PMID: 17372140 No abstract available.

4

Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutation.

Uro-Coste E, Arné-Bes MC, Pellissier JF, Richard P, Levade T, Heitz F, Figarella-Branger D, Delisle MB. Uro-Coste E, et al. Neuromuscul Disord. 2009 Feb;19(2):163-6. doi: 10.1016/j.nmd.2008.11.012. Epub 2009 Jan 12. Neuromuscul Disord. 2009. PMID: 19138847

5

Cap disease due to mutation of the beta-tropomyosin gene (TPM2).

Clarke NF, Domazetovska A, Waddell L, Kornberg A, McLean C, North KN. Clarke NF, et al. Neuromuscul Disord. 2009 May;19(5):348-51. doi: 10.1016/j.nmd.2009.03.003. Epub 2009 Apr 3. Neuromuscul Disord. 2009. PMID: 19345583

6

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy.

Nowak KJ, Wattanasirichaigoon D, Goebel HH, Wilce M, Pelin K, Donner K, Jacob RL, Hübner C, Oexle K, Anderson JR, Verity CM, North KN, Iannaccone ST, Müller CR, Nürnberg P, Muntoni F, Sewry C, Hughes I, Sutphen R, Lacson AG, Swoboda KJ, Vigneron J, Wallgren-Pettersson C, Beggs AH, Laing NG. Nowak KJ, et al. Nat Genet. 1999 Oct;23(2):208-12. doi: 10.1038/13837. Nat Genet. 1999. PMID: 10508519

7

Distinct phenotypic features and gender-specific disease manifestations in a Spanish family with desmin L370P mutation.

Arias M, Pardo J, Blanco-Arias P, Sobrido MJ, Arias S, Dapena D, Carracedo A, Goldfarb LG, Navarro C. Arias M, et al. Neuromuscul Disord. 2006 Aug;16(8):498-503. doi: 10.1016/j.nmd.2006.05.011. Epub 2006 Jun 27. Neuromuscul Disord. 2006. PMID: 16806931

8

Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy.

Carrier L, Bonne G, Bährend E, Yu B, Richard P, Niel F, Hainque B, Cruaud C, Gary F, Labeit S, Bouhour JB, Dubourg O, Desnos M, Hagège AA, Trent RJ, Komajda M, Fiszman M, Schwartz K. Carrier L, et al. Circ Res. 1997 Mar;80(3):427-34. Circ Res. 1997. PMID: 9048664

9

A series of West European patients with severe cardiac and skeletal myopathy associated with a de novo R406W mutation in desmin.

Dagvadorj A, Olivé M, Urtizberea JA, Halle M, Shatunov A, Bönnemann C, Park KY, Goebel HH, Ferrer I, Vicart P, Dalakas MC, Goldfarb LG. Dagvadorj A, et al. J Neurol. 2004 Feb;251(2):143-9. doi: 10.1007/s00415-004-0289-3. J Neurol. 2004. PMID: 14991347

10

Morphological, clinical and genetic aspects in a family with a novel LAMP-2 gene mutation (Danon disease).

Lobrinus JA, Schorderet DF, Payot M, Jeanrenaud X, Bottani A, Superti-Furga A, Schlaepfer J, Fromer M, Jeannet PY. Lobrinus JA, et al. Neuromuscul Disord. 2005 Apr;15(4):293-8. doi: 10.1016/j.nmd.2004.12.007. Neuromuscul Disord. 2005. PMID: 15792868

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