Similar articles for PMID: 15253947

Year	Number of Results
1994	1
1996	1
1998	1
2000	4
2002	2
2003	2
2004	8
2005	18
2006	6
2007	6
2008	9
2009	4
2010	4
2011	2
2012	3
2013	2
2014	2
2015	3
2016	2
2017	1
2018	5
2019	1
2021	1
2024	0

1

Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic survey.

Charron P, Villard E, Sébillon P, Laforêt P, Maisonobe T, Duboscq-Bidot L, Romero N, Drouin-Garraud V, Frébourg T, Richard P, Eymard B, Komajda M. Charron P, et al. Heart. 2004 Aug;90(8):842-6. doi: 10.1136/hrt.2003.029504. Heart. 2004. PMID: 15253947 Free PMC article.

2

Glycogen storage diseases presenting as hypertrophic cardiomyopathy.

Arad M, Maron BJ, Gorham JM, Johnson WH Jr, Saul JP, Perez-Atayde AR, Spirito P, Wright GB, Kanter RJ, Seidman CE, Seidman JG. Arad M, et al. N Engl J Med. 2005 Jan 27;352(4):362-72. doi: 10.1056/NEJMoa033349. N Engl J Med. 2005. PMID: 15673802 Free article.

3

Alport syndrome. Molecular genetic aspects.

Hertz JM. Hertz JM. Dan Med Bull. 2009 Aug;56(3):105-52. Dan Med Bull. 2009. PMID: 19728970

4

Familial and sporadic hypertrophic myopathy: differences and similarities in a genotyped population. A long follow-up study.

Brito D, Richard P, Komajda M, Madeira H. Brito D, et al. Rev Port Cardiol. 2008 Feb;27(2):147-73. Rev Port Cardiol. 2008. PMID: 18488914 English, Portuguese.

5

Prevalence of sarcomere protein gene mutations in preadolescent children with hypertrophic cardiomyopathy.

Kaski JP, Syrris P, Esteban MT, Jenkins S, Pantazis A, Deanfield JE, McKenna WJ, Elliott PM. Kaski JP, et al. Circ Cardiovasc Genet. 2009 Oct;2(5):436-41. doi: 10.1161/CIRCGENETICS.108.821314. Epub 2009 Jul 16. Circ Cardiovasc Genet. 2009. PMID: 20031618

6

Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in children.

Yang Z, McMahon CJ, Smith LR, Bersola J, Adesina AM, Breinholt JP, Kearney DL, Dreyer WJ, Denfield SW, Price JF, Grenier M, Kertesz NJ, Clunie SK, Fernbach SD, Southern JF, Berger S, Towbin JA, Bowles KR, Bowles NE. Yang Z, et al. Circulation. 2005 Sep 13;112(11):1612-7. doi: 10.1161/CIRCULATIONAHA.105.546481. Epub 2005 Sep 6. Circulation. 2005. PMID: 16144992

7

Mutation screening of the PTPN11 gene in hypertrophic cardiomyopathy.

Limongelli G, Hawkes L, Calabro R, McKenna WJ, Syrris P. Limongelli G, et al. Eur J Med Genet. 2006 Sep-Oct;49(5):426-30. doi: 10.1016/j.ejmg.2006.01.003. Epub 2006 Feb 3. Eur J Med Genet. 2006. PMID: 16488201

8

Pacemaker malfunctions in Danon's disease.

Marras E, Sciarra L, Bocchino M, Delise P. Marras E, et al. Pacing Clin Electrophysiol. 2008 Jan;31(1):125-8. doi: 10.1111/j.1540-8159.2007.00937.x. Pacing Clin Electrophysiol. 2008. PMID: 18181922

9

Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects.

Monserrat L, Hermida-Prieto M, Fernandez X, Rodríguez I, Dumont C, Cazón L, Cuesta MG, Gonzalez-Juanatey C, Peteiro J, Alvarez N, Penas-Lado M, Castro-Beiras A. Monserrat L, et al. Eur Heart J. 2007 Aug;28(16):1953-61. doi: 10.1093/eurheartj/ehm239. Epub 2007 Jul 4. Eur Heart J. 2007. PMID: 17611253

10

Hypertrophic cardiomyopathy in a Portuguese population: mutations in the myosin-binding protein C gene.

Cardim N, Perrot A, Santos S, Morgado P, Pádua M, Ferreira S, Reis RP, Monteiro C, Ferreira T, Correia JM, Osterziel KJ. Cardim N, et al. Rev Port Cardiol. 2005 Dec;24(12):1463-76. Rev Port Cardiol. 2005. PMID: 16566405 English, Portuguese.

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