Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1532-429X
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy ; volume:13 ; number:1 ; day:20 ; month:6 ; year:2011 ; pages:1-9 ; date:12.2011
Journal of cardiovascular magnetic resonance ; 13, Heft 1 (20.6.2011), 1-9, 12.2011
- Creator
-
Holmström, Miia
- Contributor
-
Kivistö, Sari
Heliö, Tiina
Jurkko, Raija
Kaartinen, Maija
Antila, Margareta
Reissell, Eeva
Kuusisto, Johanna
Kärkkäinen, Satu
Peuhkurinen, Keijo
Koikkalainen, Juha
Lötjönen, Jyrki
Lauerma, Kirsi
SpringerLink (Online service)
- DOI
-
10.1186/1532-429X-13-30
- URN
-
urn:nbn:de:1111-201603229833
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:53 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Holmström, Miia
- Kivistö, Sari
- Heliö, Tiina
- Jurkko, Raija
- Kaartinen, Maija
- Antila, Margareta
- Reissell, Eeva
- Kuusisto, Johanna
- Kärkkäinen, Satu
- Peuhkurinen, Keijo
- Koikkalainen, Juha
- Lötjönen, Jyrki
- Lauerma, Kirsi
- SpringerLink (Online service)
Other Objects (12)
Lamin A/C truncation in dilated cardiomyopathy with conduction disease
Description of A/C gene mutation related dilated cardiomyopathy with gadolinium- enhanced magnetic resonance imaging
Cardiomyopathy, familial dilated
Familial dilated cardiomyopathy caused by a novel variant in the Lamin A/C gene: a case report
Systematic in vivo candidate evaluation uncovers therapeutic targets for LMNA dilated cardiomyopathy and risk of Lamin A toxicity
Lamin A/C deficiency-mediated ROS elevation contributes to pathogenic phenotypes of dilated cardiomyopathy in iPSC model
Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death
Dilated cardiomyopathies and non-compaction cardiomyopathy
2069 Assessment of genetic dilated cardiomyopathy in LMNA-mutation carriers by cardiac MRI
Familial dilated cardiomyopathy with RBM20 mutation in an Indian patient: a case report
Extracellular volume fraction in dilated cardiomyopathy patients without obvious late gadolinium enhancement: comparison with healthy control subjects
Cardiac MRI in Evaluation of Dilated Cardiomyopathy
Lamin A/C truncation in dilated cardiomyopathy with conduction disease
Description of A/C gene mutation related dilated cardiomyopathy with gadolinium- enhanced magnetic resonance imaging
Cardiomyopathy, familial dilated
Familial dilated cardiomyopathy caused by a novel variant in the Lamin A/C gene: a case report
Systematic in vivo candidate evaluation uncovers therapeutic targets for LMNA dilated cardiomyopathy and risk of Lamin A toxicity
Lamin A/C deficiency-mediated ROS elevation contributes to pathogenic phenotypes of dilated cardiomyopathy in iPSC model
Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death
Dilated cardiomyopathies and non-compaction cardiomyopathy
2069 Assessment of genetic dilated cardiomyopathy in LMNA-mutation carriers by cardiac MRI
Familial dilated cardiomyopathy with RBM20 mutation in an Indian patient: a case report
Extracellular volume fraction in dilated cardiomyopathy patients without obvious late gadolinium enhancement: comparison with healthy control subjects
Cardiac MRI in Evaluation of Dilated Cardiomyopathy
Lamin A/C truncation in dilated cardiomyopathy with conduction disease
Description of A/C gene mutation related dilated cardiomyopathy with gadolinium- enhanced magnetic resonance imaging
Cardiomyopathy, familial dilated
Familial dilated cardiomyopathy caused by a novel variant in the Lamin A/C gene: a case report
Systematic in vivo candidate evaluation uncovers therapeutic targets for LMNA dilated cardiomyopathy and risk of Lamin A toxicity
Lamin A/C deficiency-mediated ROS elevation contributes to pathogenic phenotypes of dilated cardiomyopathy in iPSC model
Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death
Dilated cardiomyopathies and non-compaction cardiomyopathy
2069 Assessment of genetic dilated cardiomyopathy in LMNA-mutation carriers by cardiac MRI
Familial dilated cardiomyopathy with RBM20 mutation in an Indian patient: a case report
Extracellular volume fraction in dilated cardiomyopathy patients without obvious late gadolinium enhancement: comparison with healthy control subjects