-
1
-
-
84860237424
-
Clonally dominant cardiomyocytes direct heart morphogenesis
-
Gupta V, Poss KD. Clonally dominant cardiomyocytes direct heart morphogenesis. Nature. 2012;484:479-484. doi: 10. 1038/nature11045.
-
(2012)
Nature.
, vol.484
, pp. 479-484
-
-
Gupta, V.1
Poss, K.D.2
-
2
-
-
84908179714
-
Left ventricular noncompaction: A distinct cardiomyopathy or a trait shared by different cardiac diseases?
-
Arbustini E, Weidemann F, Hall JL. Left ventricular noncompaction: a distinct cardiomyopathy or a trait shared by different cardiac diseases? J Am Coll Cardiol. 2014;64:1840-1850. doi: 10. 1016/j. jacc. 2014. 08. 030.
-
(2014)
J Am Coll Cardiol.
, vol.64
, pp. 1840-1850
-
-
Arbustini, E.1
Weidemann, F.2
Hall, J.L.3
-
3
-
-
84880702619
-
Left ventricular non-compaction: Prevalence in congenital heart disease
-
Stähli BE, Gebhard C, Biaggi P, Klaassen S, Valsangiacomo Buechel E, Attenhofer Jost CH, et al. Left ventricular non-compaction: prevalence in congenital heart disease. Int J Cardiol. 2013;167:2477-2481. doi: 10. 1016/j. ijcard. 2012. 05. 095.
-
(2013)
Int J Cardiol.
, vol.167
, pp. 2477-2481
-
-
Stähli, B.E.1
Gebhard, C.2
Biaggi, P.3
Klaassen, S.4
Valsangiacomo Buechel, E.5
Attenhofer Jost, C.H.6
-
4
-
-
33646693410
-
Contemporary definitions and classification of the cardiomyopathies: An American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; And Council on Epidemiology and Prevention
-
American Heart Association; Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; Council on Epidemiology and Prevention
-
Maron BJ, Towbin JA, Thiene G, Antzelevitch C, Corrado D, Arnett D, et al; American Heart Association; Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; Council on Epidemiology and Prevention. Contemporary definitions and classification of the cardiomyopathies: an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention. Circulation. 2006;113:1807-1816. doi: 10. 1161/CIRCULATIONAHA. 106. 174287.
-
(2006)
Circulation.
, vol.113
, pp. 1807-1816
-
-
Maron, B.J.1
Towbin, J.A.2
Thiene, G.3
Antzelevitch, C.4
Corrado, D.5
Arnett, D.6
-
5
-
-
33748039745
-
Different types of cardiomyopathy associated with isolated ventricular noncompaction
-
Biagini E, Ragni L, Ferlito M, Pasquale F, Lofiego C, Leone O, et al. Different types of cardiomyopathy associated with isolated ventricular noncompaction. Am J Cardiol. 2006;98:821-824. doi: 10. 1016/j. amjcard. 2006. 04. 021.
-
(2006)
Am J Cardiol.
, vol.98
, pp. 821-824
-
-
Biagini, E.1
Ragni, L.2
Ferlito, M.3
Pasquale, F.4
Lofiego, C.5
Leone, O.6
-
6
-
-
85006256556
-
Long-term prognostic value of cardiac magnetic resonance in left ventricle noncompaction: A prospective multicenter study
-
Andreini D, Pontone G, Bogaert J, Roghi A, Barison A, Schwitter J, et al. Long-term prognostic value of cardiac magnetic resonance in left ventricle noncompaction: a prospective multicenter study. J Am Coll Cardiol. 2016;68:2166-2181. doi: 10. 1016/j. jacc. 2016. 08. 053.
-
(2016)
J Am Coll Cardiol.
, vol.68
, pp. 2166-2181
-
-
Andreini, D.1
Pontone, G.2
Bogaert, J.3
Roghi, A.4
Barison, A.5
Schwitter, J.6
-
7
-
-
80052752591
-
Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype
-
Probst S, Oechslin E, Schuler P, Greutmann M, Boyé P, Knirsch W, et al. Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype. Circ Cardiovasc Genet. 2011;4:367-374. doi: 10. 1161/CIRCGENETICS. 110. 959270.
-
(2011)
Circ Cardiovasc Genet.
, vol.4
, pp. 367-374
-
-
Probst, S.1
Oechslin, E.2
Schuler, P.3
Greutmann, M.4
Boyé, P.5
Knirsch, W.6
-
8
-
-
44649118695
-
Mutations in sarcomere protein genes in left ventricular noncompaction
-
Klaassen S, Probst S, Oechslin E, Gerull B, Krings G, Schuler P, et al. Mutations in sarcomere protein genes in left ventricular noncompaction. Circulation. 2008;117:2893-2901. doi: 10. 1161/ CIRCULATIONAHA. 107. 746164.
-
(2008)
Circulation.
, vol.117
, pp. 2893-2901
-
-
Klaassen, S.1
Probst, S.2
Oechslin, E.3
Gerull, B.4
Krings, G.5
Schuler, P.6
-
9
-
-
77955880540
-
The importance of genetic counseling, DNA diagnostics, and cardiologic family screening in left ventricular noncompaction cardiomyopathy
-
Hoedemaekers YM, Caliskan K, Michels M, Frohn-Mulder I, van der Smagt JJ, Phefferkorn JE, et al. The importance of genetic counseling, DNA diagnostics, and cardiologic family screening in left ventricular noncompaction cardiomyopathy. Circ Cardiovasc Genet. 2010;3:232-239. doi: 10. 1161/CIRCGENETICS. 109. 903898.
-
(2010)
Circ Cardiovasc Genet.
, vol.3
, pp. 232-239
-
-
Hoedemaekers, Y.M.1
Caliskan, K.2
Michels, M.3
Frohn-Mulder, I.4
Van Der Smagt, J.J.5
Phefferkorn, J.E.6
-
10
-
-
77949887523
-
Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation
-
Dellefave LM, Pytel P, Mewborn S, Mora B, Guris DL, Fedson S, et al. Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation. Circ Cardiovasc Genet. 2009;2:442-449. doi: 10. 1161/ CIRCGENETICS. 109. 861955.
-
(2009)
Circ Cardiovasc Genet.
, vol.2
, pp. 442-449
-
-
Dellefave, L.M.1
Pytel, P.2
Mewborn, S.3
Mora, B.4
Guris, D.L.5
Fedson, S.6
-
11
-
-
84880702275
-
Implications of genetic testing in noncompaction/hypertrabeculation
-
Shieh JT. Implications of genetic testing in noncompaction/hypertrabeculation. Am J Med Genet C Semin Med Genet. 2013;163C:206-211.
-
(2013)
Am J Med Genet C Semin Med Genet.
, vol.163
, Issue.C
, pp. 206-211
-
-
Shieh, J.T.1
-
12
-
-
84860457415
-
Pediatric cardiomyopathy: Importance of genetic and metabolic evaluation
-
Kindel SJ, Miller EM, Gupta R, Cripe LH, Hinton RB, Spicer RL, et al. Pediatric cardiomyopathy: importance of genetic and metabolic evaluation. J Card Fail. 2012;18:396-403. doi: 10. 1016/j. cardfail. 2012. 01. 017.
-
(2012)
J Card Fail.
, vol.18
, pp. 396-403
-
-
Kindel, S.J.1
Miller, E.M.2
Gupta, R.3
Cripe, L.H.4
Hinton, R.B.5
Spicer, R.L.6
-
13
-
-
62049084378
-
Research electronic data capture (REDCap)-a metadata-driven methodology and workflow process for providing translational research informatics support
-
Harris PA, Taylor R, Thielke R, Payne J, Gonzalez N, Conde JG. Research electronic data capture (REDCap)-a metadata-driven methodology and workflow process for providing translational research informatics support. J Biomed Inform. 2009;42:377-381. doi: 10. 1016/j. jbi. 2008. 08. 010.
-
(2009)
J Biomed Inform.
, vol.42
, pp. 377-381
-
-
Harris, P.A.1
Taylor, R.2
Thielke, R.3
Payne, J.4
Gonzalez, N.5
Conde, J.G.6
-
14
-
-
17044449684
-
Left ventricular hypertrabeculation/noncompaction
-
Stöllberger C, Finsterer J. Left ventricular hypertrabeculation/noncompaction. J Am Soc Echocardiogr. 2004;17:91-100. doi: 10. 1016/ S0894-7317(03)00514-5.
-
(2004)
J Am Soc Echocardiogr.
, vol.17
, pp. 91-100
-
-
Stöllberger, C.1
Finsterer, J.2
-
15
-
-
0035185141
-
Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: A step towards classification as a distinct cardiomyopathy
-
Jenni R, Oechslin E, Schneider J, Attenhofer Jost C, Kaufmann PA. Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy. Heart. 2001;86:666-671.
-
(2001)
Heart.
, vol.86
, pp. 666-671
-
-
Jenni, R.1
Oechslin, E.2
Schneider, J.3
Attenhofer Jost, C.4
Kaufmann, P.A.5
-
16
-
-
85015452634
-
Rationale for the cytogenomics of cardiovascular malformations consortium: A phenotype intensive registry based approach
-
Hinton RB, McBride KL, Bleyl SB, Bowles NE, Border WL, Garg V, et al. Rationale for the cytogenomics of cardiovascular malformations consortium: a phenotype intensive registry based approach. J Cardiovasc Dev Dis. 2015;2:76-92.
-
(2015)
J Cardiovasc Dev Dis.
, vol.2
, pp. 76-92
-
-
Hinton, R.B.1
McBride, K.L.2
Bleyl, S.B.3
Bowles, N.E.4
Border, W.L.5
Garg, V.6
-
17
-
-
35348837913
-
Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies
-
National Birth Defects Prevention Study
-
Botto LD, Lin AE, Riehle-Colarusso T, Malik S, Correa A; National Birth Defects Prevention Study. Seeking causes: classifying and evaluating congenital heart defects in etiologic studies. Birth Defects Res A Clin Mol Teratol. 2007;79:714-727. doi: 10. 1002/bdra. 20403.
-
(2007)
Birth Defects Res A Clin Mol Teratol.
, vol.79
, pp. 714-727
-
-
Botto, L.D.1
Lin, A.E.2
Riehle-Colarusso, T.3
Malik, S.4
Correa, A.5
-
18
-
-
84928209346
-
Standards and guidelines for the interpretation of sequence variants: A joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
-
ACMG Laboratory Quality Assurance Committee
-
Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, et al; ACMG Laboratory Quality Assurance Committee. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med. 2015;17:405-424. doi: 10. 1038/gim. 2015. 30.
-
(2015)
Genet Med.
, vol.17
, pp. 405-424
-
-
Richards, S.1
Aziz, N.2
Bale, S.3
Bick, D.4
Das, S.5
Gastier-Foster, J.6
-
19
-
-
0033953776
-
Design and implementation of the North American Pediatric Cardiomyopathy Registry
-
Grenier MA, Osganian SK, Cox GF, Towbin JA, Colan SD, Lurie PR, et al. Design and implementation of the North American Pediatric Cardiomyopathy Registry. Am Heart J. 2000;139(2 pt 3):S86-S95.
-
(2000)
Am Heart J.
, vol.139
, Issue.2
, pp. S86-S95
-
-
Grenier, M.A.1
Osganian, S.K.2
Cox, G.F.3
Towbin, J.A.4
Colan, S.D.5
Lurie, P.R.6
-
20
-
-
84982253941
-
Analysis of protein-coding genetic variation in 60, 706 humans
-
Exome Aggregation Consortium
-
Lek M, Karczewski KJ, Minikel EV, Samocha KE, Banks E, Fennell T, et al; Exome Aggregation Consortium. Analysis of protein-coding genetic variation in 60, 706 humans. Nature. 2016;536:285-291. doi: 10. 1038/ nature19057.
-
(2016)
Nature.
, vol.536
, pp. 285-291
-
-
Lek, M.1
Karczewski, K.J.2
Minikel, E.V.3
Samocha, K.E.4
Banks, E.5
Fennell, T.6
-
21
-
-
84939473792
-
Exon 3 deletion of ryanodine receptor causes left ventricular noncompaction, worsening catecholaminergic polymorphic ventricular tachycardia, and sudden cardiac arrest
-
Campbell MJ, Czosek RJ, Hinton RB, Miller EM. Exon 3 deletion of ryanodine receptor causes left ventricular noncompaction, worsening catecholaminergic polymorphic ventricular tachycardia, and sudden cardiac arrest. Am J Med Genet A. 2015;167A:2197-2200. doi: 10. 1002/ ajmg. a. 37140.
-
(2015)
Am J Med Genet A.
, vol.167
, Issue.A
, pp. 2197-2200
-
-
Campbell, M.J.1
Czosek, R.J.2
Hinton, R.B.3
Miller, E.M.4
-
22
-
-
79960867817
-
HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)
-
Ackerman MJ, Priori SG, Willems S, Berul C, Brugada R, Calkins H, et al. HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA). Heart Rhythm. 2011;8:1308-1339. doi: 10. 1016/j. hrthm. 2011. 05. 020.
-
(2011)
Heart Rhythm.
, vol.8
, pp. 1308-1339
-
-
Ackerman, M.J.1
Priori, S.G.2
Willems, S.3
Berul, C.4
Brugada, R.5
Calkins, H.6
-
23
-
-
84928235886
-
Reference values for left and right ventricular trabeculation and noncompacted myocardium
-
André F, Burger A, Losnitzer D, Buss SJ, Abdel-Aty H, Gianntisis E, et al. Reference values for left and right ventricular trabeculation and noncompacted myocardium. Int J Cardiol. 2015;185:240-247. doi: 10. 1016/j. ijcard. 2015. 03. 065.
-
(2015)
Int J Cardiol.
, vol.185
, pp. 240-247
-
-
André, F.1
Burger, A.2
Losnitzer, D.3
Buss, S.J.4
Abdel-Aty, H.5
Gianntisis, E.6
-
24
-
-
84909588138
-
Characteristics of trabeculated myocardium burden in young and apparently healthy adults
-
Tizón-Marcos H, de la Paz Ricapito M, Pibarot P, Bertrand O, Bibeau K, Le Ven F, et al. Characteristics of trabeculated myocardium burden in young and apparently healthy adults. Am J Cardiol. 2014;114:1094-1099. doi: 10. 1016/j. amjcard. 2014. 07. 025.
-
(2014)
Am J Cardiol.
, vol.114
, pp. 1094-1099
-
-
Tizón-Marcos, H.1
De La Paz Ricapito, M.2
Pibarot, P.3
Bertrand, O.4
Bibeau, K.5
Le Ven, F.6
-
25
-
-
84886727423
-
Left ventricular noncompaction in patients with bicuspid aortic valve
-
Agarwal A, Khandheria BK, Paterick TE, Treiber SC, Bush M, Tajik AJ. Left ventricular noncompaction in patients with bicuspid aortic valve. J Am Soc Echocardiogr. 2013;26:1306-1313. doi: 10. 1016/j. echo. 2013. 08. 003.
-
(2013)
J Am Soc Echocardiogr.
, vol.26
, pp. 1306-1313
-
-
Agarwal, A.1
Khandheria, B.K.2
Paterick, T.E.3
Treiber, S.C.4
Bush, M.5
Tajik, A.J.6
-
26
-
-
84976384440
-
The impact of concomitant left ventricular non-compaction with congenital heart disease on perioperative outcomes
-
Ramachandran P, Woo JG, Ryan TD, Bryant R, Heydarian HC, Jefferies JL, et al. The impact of concomitant left ventricular non-compaction with congenital heart disease on perioperative outcomes. Pediatr Cardiol. 2016;37:1307-1312. doi: 10. 1007/s00246-016-1435-2.
-
(2016)
Pediatr Cardiol.
, vol.37
, pp. 1307-1312
-
-
Ramachandran, P.1
Woo, J.G.2
Ryan, T.D.3
Bryant, R.4
Heydarian, H.C.5
Jefferies, J.L.6
-
27
-
-
84946473891
-
Cardiomyopathy phenotypes and outcomes for children with left ventricular myocardial noncompaction: Results from the Pediatric Cardiomyopathy Registry
-
Jefferies JL, Wilkinson JD, Sleeper LA, Colan SD, Lu M, Pahl E, et al; Pediatric Cardiomyopathy Registry Investigators. Cardiomyopathy phenotypes and outcomes for children with left ventricular myocardial noncompaction: results from the Pediatric Cardiomyopathy Registry. J Card Fail. 2015;21:877-884. doi: 10. 1016/j. cardfail. 2015. 06. 381.
-
(2015)
J Card Fail.
, vol.21
, pp. 877-884
-
-
Jefferies, J.L.1
Wilkinson, J.D.2
Sleeper, L.A.3
Colan, S.D.4
Lu, M.5
Pahl, E.6
-
28
-
-
85011933920
-
Reassessment of Mendelian gene pathogenicity using 7, 855 cardiomyopathy cases and 60, 706 reference samples
-
Walsh R, Thomson KL, Ware JS, Funke BH, Woodley J, McGuire KJ, et al. Reassessment of Mendelian gene pathogenicity using 7, 855 cardiomyopathy cases and 60, 706 reference samples. Genet Med. 2017;19:192-203. doi: 10. 1038/gim. 2016. 90.
-
(2017)
Genet Med.
, vol.19
, pp. 192-203
-
-
Walsh, R.1
Thomson, K.L.2
Ware, J.S.3
Funke, B.H.4
Woodley, J.5
McGuire, K.J.6
-
29
-
-
84867720848
-
Inhibition of Notch2 by Numb/Numblike controls myocardial compaction in the heart
-
Yang J, Bücker S, Jungblut B, Böttger T, Cinnamon Y, Tchorz J, et al. Inhibition of Notch2 by Numb/Numblike controls myocardial compaction in the heart. Cardiovasc Res. 2012;96:276-285. doi: 10. 1093/cvr/cvs250.
-
(2012)
Cardiovasc Res.
, vol.96
, pp. 276-285
-
-
Yang, J.1
Bücker, S.2
Jungblut, B.3
Böttger, T.4
Cinnamon, Y.5
Tchorz, J.6
-
30
-
-
84875981663
-
Fkbp1a controls ventricular myocardium trabeculation and compaction by regulating endocardial Notch1 activity
-
Chen H, Zhang W, Sun X, Yoshimoto M, Chen Z, Zhu W, et al. Fkbp1a controls ventricular myocardium trabeculation and compaction by regulating endocardial Notch1 activity. Development. 2013;140:1946-1957. doi: 10. 1242/dev. 089920.
-
(2013)
Development.
, vol.140
, pp. 1946-1957
-
-
Chen, H.1
Zhang, W.2
Sun, X.3
Yoshimoto, M.4
Chen, Z.5
Zhu, W.6
-
31
-
-
84873536788
-
Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy
-
Luxán G, Casanova JC, Martínez-Poveda B, Prados B, D'Amato G, Mac-Grogan D, et al. Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy. Nat Med. 2013;19:193-201. doi: 10. 1038/nm. 3046.
-
(2013)
Nat Med.
, vol.19
, pp. 193-201
-
-
Luxán, G.1
Casanova, J.C.2
Martínez-Poveda, B.3
Prados, B.4
D'Amato, G.5
Mac-Grogan, D.6
|