Format
Sort by

Send to

Choose Destination

Search results

Items: 10

1.

Early onset cardiomyopathy in females with Danon disease.

Hedberg Oldfors C, Máthé G, Thomson K, Tulinius M, Karason K, Östman-Smith I, Oldfors A.

Neuromuscul Disord. 2015 Jun;25(6):493-501. doi: 10.1016/j.nmd.2015.03.005. Epub 2015 Mar 16.

PMID:
25900304
2.

Asymptomatic young man with Danon disease.

Kim J, Parikh P, Mahboob M, Arrighi JA, Atalay MK, Rowin EJ, Maron MS.

Tex Heart Inst J. 2014 Jun 1;41(3):332-4. doi: 10.14503/THIJ-13-3279. eCollection 2014 Jun.

3.

Advantages of a subcutaneous implantable cardioverter-defibrillator in LAMP2 hypertrophic cardiomyopathy.

Zaki A, Zaidi A, Newman WG, Garratt CJ.

J Cardiovasc Electrophysiol. 2013 Sep;24(9):1051-3. doi: 10.1111/jce.12142. Epub 2013 Apr 11.

PMID:
23577876
4.

Sudden death associated with danon disease in women.

Miani D, Taylor M, Mestroni L, D'Aurizio F, Finato N, Fanin M, Brigido S, Proclemer A.

Am J Cardiol. 2012 Feb 1;109(3):406-11. doi: 10.1016/j.amjcard.2011.09.024. Epub 2011 Nov 9.

PMID:
22074992
5.

Cardiovascular magnetic resonance findings in a case of Danon disease.

Piotrowska-Kownacka D, Kownacki L, Kuch M, Walczak E, Kosieradzka A, Fidzianska A, Krolicki L.

J Cardiovasc Magn Reson. 2009 Apr 29;11:12. doi: 10.1186/1532-429X-11-12.

6.

Clinical outcome and phenotypic expression in LAMP2 cardiomyopathy.

Maron BJ, Roberts WC, Arad M, Haas TS, Spirito P, Wright GB, Almquist AK, Baffa JM, Saul JP, Ho CY, Seidman J, Seidman CE.

JAMA. 2009 Mar 25;301(12):1253-9. doi: 10.1001/jama.2009.371.

7.

Novel Lamp-2 gene mutation and successful treatment with heart transplantation in a large family with Danon disease.

Echaniz-Laguna A, Mohr M, Epailly E, Nishino I, Charron P, Richard P, Guiraud-Chaumeil C, Tranchant C.

Muscle Nerve. 2006 Mar;33(3):393-7.

PMID:
16372318
8.

Familial X-linked cardiomyopathy (Danon disease): diagnostic confirmation by mutation analysis of the LAMP2gene.

Balmer C, Ballhausen D, Bosshard NU, Steinmann B, Boltshauser E, Bauersfeld U, Superti-Furga A.

Eur J Pediatr. 2005 Aug;164(8):509-14. Epub 2005 May 12.

PMID:
15889279
9.

Identification of a novel LAMP2 mutation responsible for X-chromosomal dominant Danon disease.

Horváth J, Ketelsen UP, Geibel-Zehender A, Boehm N, Olbrich H, Korinthenberg R, Omran H.

Neuropediatrics. 2003 Jun;34(5):270-3.

PMID:
14598234
10.

Lysosomal glycogen storage disease with normal acid maltase with early fatal outcome.

Morisawa Y, Fujieda M, Murakami N, Naruse K, Okada T, Morita H, Sawada K, Miyazaki J, Kurashige T, Nonaka I.

J Neurol Sci. 1998 Oct 8;160(2):175-9.

PMID:
9849802
Items per page

Supplemental Content

Loading ...
Write to the Help Desk