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Items: 1 to 20 of 160

1.

Risk prediction of ventricular arrhythmias and myocardial function in Lamin A/C mutation positive subjects.

Hasselberg NE, Edvardsen T, Petri H, Berge KE, Leren TP, Bundgaard H, Haugaa KH.

Europace. 2014 Apr;16(4):563-71. doi: 10.1093/europace/eut291. Epub 2013 Sep 20.

PMID:
24058181
2.

Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy.

Holmström M, Kivistö S, Heliö T, Jurkko R, Kaartinen M, Antila M, Reissell E, Kuusisto J, Kärkkäinen S, Peuhkurinen K, Koikkalainen J, Lötjönen J, Lauerma K.

J Cardiovasc Magn Reson. 2011 Jun 20;13:30. doi: 10.1186/1532-429X-13-30.

3.

Mechanical dispersion assessed by myocardial strain in patients after myocardial infarction for risk prediction of ventricular arrhythmia.

Haugaa KH, Smedsrud MK, Steen T, Kongsgaard E, Loennechen JP, Skjaerpe T, Voigt JU, Willems R, Smith G, Smiseth OA, Amlie JP, Edvardsen T.

JACC Cardiovasc Imaging. 2010 Mar;3(3):247-56. doi: 10.1016/j.jcmg.2009.11.012.

4.

Cardiac Mechanical Alterations and Genotype Specific Differences in Subjects With Long QT Syndrome.

Leren IS, Hasselberg NE, Saberniak J, Håland TF, Kongsgård E, Smiseth OA, Edvardsen T, Haugaa KH.

JACC Cardiovasc Imaging. 2015 May;8(5):501-510. doi: 10.1016/j.jcmg.2014.12.023. Epub 2015 Apr 15.

5.

Mid-myocardial fibrosis by cardiac magnetic resonance in patients with lamin A/C cardiomyopathy: possible substrate for diastolic dysfunction.

Raman SV, Sparks EA, Baker PM, McCarthy B, Wooley CF.

J Cardiovasc Magn Reson. 2007;9(6):907-13.

PMID:
18066751
6.

Long-Term Arrhythmic and Nonarrhythmic Outcomes of Lamin A/C Mutation Carriers.

Kumar S, Baldinger SH, Gandjbakhch E, Maury P, Sellal JM, Androulakis AF, Waintraub X, Charron P, Rollin A, Richard P, Stevenson WG, Macintyre CJ, Ho CY, Thompson T, Vohra JK, Kalman JM, Zeppenfeld K, Sacher F, Tedrow UB, Lakdawala NK.

J Am Coll Cardiol. 2016 Nov 29;68(21):2299-2307. doi: 10.1016/j.jacc.2016.08.058.

PMID:
27884249
7.

Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complications.

van Rijsingen IA, Bakker A, Azim D, Hermans-van Ast JF, van der Kooi AJ, van Tintelen JP, van den Berg MP, Christiaans I, Lekanne Dit Deprez RH, Wilde AA, Zwinderman AH, Meijers JC, Grootemaat AE, Nieuwland R, Pinto YM, Pinto-Sietsma SJ.

Int J Cardiol. 2013 Sep 20;168(1):472-7. doi: 10.1016/j.ijcard.2012.09.118. Epub 2012 Oct 14.

8.

[A novel lamin A/C mutation in a family with dilated cardiomyopathy and a strong history of sudden cardiac death].

Andreassi MG, Botto N, Vittorini S, Pulignani S, Aquaro G, Sicari R.

Recenti Prog Med. 2010 Mar;101(3):127-30. Italian.

PMID:
20461955
10.

Myocardial fibrosis as a key determinant of left ventricular remodeling in idiopathic dilated cardiomyopathy: a contrast-enhanced cardiovascular magnetic study.

Masci PG, Schuurman R, Andrea B, Ripoli A, Coceani M, Chiappino S, Todiere G, Srebot V, Passino C, Aquaro GD, Emdin M, Lombardi M.

Circ Cardiovasc Imaging. 2013 Sep;6(5):790-9. doi: 10.1161/CIRCIMAGING.113.000438. Epub 2013 Aug 9.

11.

Lamin A/C gene mutations in familial cardiomyopathy with advanced atrioventricular block and arrhythmia.

Saga A, Karibe A, Otomo J, Iwabuchi K, Takahashi T, Kanno H, Kikuchi J, Keitoku M, Shinozaki T, Shimokawa H.

Tohoku J Exp Med. 2009 Aug;218(4):309-16.

12.

Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.

van Rijsingen IA, Nannenberg EA, Arbustini E, Elliott PM, Mogensen J, Hermans-van Ast JF, van der Kooi AJ, van Tintelen JP, van den Berg MP, Grasso M, Serio A, Jenkins S, Rowland C, Richard P, Wilde AA, Perrot A, Pankuweit S, Zwinderman AH, Charron P, Christiaans I, Pinto YM.

Eur J Heart Fail. 2013 Apr;15(4):376-84. doi: 10.1093/eurjhf/hfs191. Epub 2012 Nov 25.

13.

Tetralogy of Fallot: impact of the excursion of the interventricular septum on left ventricular systolic function and fibrosis after surgical repair.

Muzzarelli S, Ordovas KG, Cannavale G, Meadows AK, Higgins CB.

Radiology. 2011 May;259(2):375-83. doi: 10.1148/radiol.10100895. Epub 2011 Jan 19.

PMID:
21248236
14.

N-terminal Pro brain natriuretic peptide is a reliable biomarker of reduced myocardial contractility in patients with lamin A/C gene mutations.

Meune C, Wahbi K, Gobeaux C, Duboc D, Pecker F, Bonne G.

Int J Cardiol. 2011 Sep 1;151(2):160-3. doi: 10.1016/j.ijcard.2010.05.005. Epub 2010 Jul 23.

PMID:
20627339
15.

Prognostic value of myocardial fibrosis in patients with severe aortic valve stenosis.

Milano AD, Faggian G, Dodonov M, Golia G, Tomezzoli A, Bortolotti U, Mazzucco A.

J Thorac Cardiovasc Surg. 2012 Oct;144(4):830-7. doi: 10.1016/j.jtcvs.2011.11.024. Epub 2012 Jan 12.

16.

Impaired hyperemic myocardial blood flow is associated with inducibility of ventricular arrhythmia in ischemic cardiomyopathy.

Rijnierse MT, de Haan S, Harms HJ, Robbers LF, Wu L, Danad I, Beek AM, Heymans MW, van Rossum AC, Lammertsma AA, Allaart CP, Knaapen P.

Circ Cardiovasc Imaging. 2014 Jan;7(1):20-30. doi: 10.1161/CIRCIMAGING.113.001158. Epub 2013 Dec 16.

17.

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.

Fatkin D, MacRae C, Sasaki T, Wolff MR, Porcu M, Frenneaux M, Atherton J, Vidaillet HJ Jr, Spudich S, De Girolami U, Seidman JG, Seidman C, Muntoni F, Müehle G, Johnson W, McDonough B.

N Engl J Med. 1999 Dec 2;341(23):1715-24.

18.

Structural and electrical cardiac abnormalities are prevalent in asymptomatic adults with myotonic dystrophy.

Choudhary P, Nandakumar R, Greig H, Broadhurst P, Dean J, Puranik R, Celermajer DS, Hillis GS.

Heart. 2016 Sep 15;102(18):1472-8. doi: 10.1136/heartjnl-2015-308517. Epub 2016 May 10.

PMID:
27164920
19.

Cardiovascular magnetic resonance of cardiomyopathy in limb girdle muscular dystrophy 2B and 2I.

Rosales XQ, Moser SJ, Tran T, McCarthy B, Dunn N, Habib P, Simonetti OP, Mendell JR, Raman SV.

J Cardiovasc Magn Reson. 2011 Aug 4;13:39. doi: 10.1186/1532-429X-13-39.

20.

Cardiac involvement in patients with lamin A/C gene mutations: a cohort observation.

Carboni N, Sardu C, Cocco E, Marrosu G, Manzi RC, Nissardi V, Isola F, Mateddu A, Solla E, Maioli MA, Oppo V, Piras R, Coghe G, Lai C, Marrosu MG.

Muscle Nerve. 2012 Aug;46(2):187-92. doi: 10.1002/mus.23294.

PMID:
22806367

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