Download Data supplement 2 - Heart

ADDITIONAL REFERENCES (online version)
Bernanke DH, Velkey JM. Development of the coronary blood supply: changing
concepts and current ideas. Anat Rec. 2002;269:198–208
Grant RT. An unusual anomaly of the coronary vessels in the malformed heart of a child.
Heart 1926;13:273–283.
Biagini E, Ragni L, Ferlito M, et al. Different types of cardiomyopathy associated with
isolated ventricular noncompaction. Am J Cardiol 2006; 98:821–824
Monserrat L, Hermida-Prieto M, Fernandez X, et al. Mutation in the alphacardiac actin
gene associated with apical hypertrophic cardiomyopathy, left ventricular
noncompaction, and septal defects. Eur Heart J 2007; 28:1953– 1961.
Lilje C, Razek V, Joyce JJ et al. Complications of noncompaction of the left ventricular
myocardium in a paediatric population: a prospective study. Eur Heart J 2006;27:1855–
1860
Kovacevic-Preradovic T, Jenni R, Oechslin EN et al. Isolated left ventricular
noncompaction as a cause for heart failure and heart transplantation: a single center
experience. Cardiology 2009;112:158–164
Richardson P, McKenna W, Bristow M et al. Report of the 1995 World Health
Organization/ International Society and Federation of Cardiology Task Force on the
Definition and Classification of cardiomyopathies. Circulation 1996;93:841–842.
Maron BJ, Towbin JA, Thiene G et al. 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.
Elliott P, Andersson B, Arbustini E et al. Classification of the cardiomyopathies: A
position statement from the European Society Of Cardiology Working Group on
Myocardial and Pericardial Diseases. Eur Heart J 2008;29:270–276
Finsterer J, Stollberger C. Definite, probable, or possible
hypertrabeculation/noncompaction. Int J Cardiol 2008;123:175–176
left
ventricular
Vrancken Peeters MPFM, Gittenberger-de Groot AC, Mentink MMT et al. The
development of the coronary vessels and their differentiation into arteries and veins in
the embryonic quail heart. Dev Dyn 1997;208:338–348.
Bartram U, Bauer J, Schranz D. Primary noncompaction of the ventricular myocardium
from the morphogenetic standpoint. Pediatr Cardiol 2007;28:325–332.
Burke A, Mont E, Kutys R, Virmani R. Left ventricular noncompaction: a pathological
study of 14 cases. Hum Pathol 2005;36:403–411
Fazio G, Novo G, Casalicchio C et al. Left ventricular non-compaction cardiomyopathy in
children: Is segmental fibrosis the cause of tissue Doppler alterations and of EF
reduction? Int J Cardiol 2009;132:278-80
Soler R, RodrıÍguez E, Monserrat L, Alvarez N. MRI of subendocardial perfusion deficits
in isolated left ventricular noncompaction. J Comput Assist Tomogr 2002;26:373–375
Borges AC, Kivelitz D, Baumann G. Isolated left ventricular non-compaction:
cardiomyopathy with homogeneous transmural and heterogeneous segmental perfusion.
Heart 2003;89:e21
Xing Y, Ichida F, Matsuoka T, et al. Genetic analysis in patients with left ventricular
noncompaction and evidence for genetic heterogeneity. Mol Genet Metab 2006;88:71–
77.
Sasse-Klaassen S, Gerull B, Oechslin E, et al. Isolated noncompaction of the left
ventricular myocardium in the adult is an autosomal dominant disorder in the majority of
patients. Am J Med Genet A 2003;119:162–167.
Bleyl SB, Mumford BR, Thompson V et al. Neonatal, lethal noncompaction of the left
ventricular myocardium is allelic with Barth syndrome. Am J Hum Genet 1997;61:868–
872
Bione S, D’Adamo P, Maestrini E, et al. A novel X-linked gene, G4.5 is responsible for
Barth syndrome. Nat Genet 1996;12:385–389.
Kenton AB, Sanchez X, Coveler KJ, et al. Isolated left ventricular noncompaction is
rarely caused by mutations in G4.5, a-dystrobrevin and FK binding protein-12. Mol
Genet Metab 2004;82:162–166.
Vatta M, Mohapatra B, Jimenez S, et al. Mutations in cypher/ZASP in patientswith
dilated cardiomyopathy and left ventricular noncompaction. J Am Coll Cardiol
2003;42:2014–2027
Hermida-Prieto M, Monserrat L, Castro-Beiras A, et al. Familial dilated cardiomyopathy
and isolated left ventricular noncompaction associated with lamin A/C gene mutations.
Am J Cardiol 2004;94:50–54
Chang B, Nishizawa T, Furutani M et al. Identi!cation of a novel TPM1 mutation in a
family with left ventricular noncompaction and sudden death. Mol Genet Metab
2011;102; 200–206
Pfammatter JP, Paul T, Flik J, et al. Q-fever associated myocarditis in a 14-year-old boy.
Z Kardiol 1995;84:947–950.
Finsterer J, Stöllberger C, Gaismayer K, Janssen B. Acquired noncompaction in
Duchenne muscular dystrophy. Int J Cardiol 2006;106:420–421
Valdes-Dapena M, Gilbert-Barness E. Cardiovascular causes for sudden infant death.
Pediatr Pathol Mol Med 2002;21:195–211.
Chahal NS, Senior R. Clinical applications of left ventricular opacification. J Am Coll
Cardiol Img 2010;3:188–96
Oda Y, Tsunoda S, Doue T, Iida Y, Matsubara H. Clinical characteristics and
morphologic features of isolated noncompaction of the ventricular myocardium:
electrocardiogram-gated magnetic resonance imaging can elucidate more accurate
biventricular structures. Heart Vessels 2005;20:126–127
Steffel J, Kobza R, Oechslin E, Jenni R, Duru F. Electrocardiographic characteristics at
initial diagnosis in patients with isolated left ventricular noncompaction. Am J Cardiol
2009;104:984–989
Ackerman MJ, Priori SG, Willems S 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). Europace. 2011;13:1077-1109
Kovacevic-Preradovic T, Jenni R, Oechslin EN et al. Isolated left ventricular
noncompaction as a cause for heart failure and heart transplantation: a single center
experience. Cardiology 2009;112:158-164
Stöllberger C, Blazek G, Wegner C, Winkler-Dworak M, Finsterer J. Neuromuscular and
cardiac comorbidity determines survival in 140 patients with left ventricular
hypertrabeculation/noncompaction. Int J Cardiol. 2011;150:71-74
Kelley-Hedgepeth A, Towbin JA and Maron MS. Overlapping Phenotypes Left
Ventricular
Noncompaction
and
Hypertrophic
Cardiomyopathy.
Circulation.
2009;119:e588-e589