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Quoted phrase not found in phrase index: "Right ventricular noncompaction cardiomyopathy"
Page 1
Cardiomyopathy: An Overview.
Brieler J, Breeden MA, Tucker J. Brieler J, et al. Am Fam Physician. 2017 Nov 15;96(10):640-646. Am Fam Physician. 2017. PMID: 29431384 Free article. Review.
Hypertrophic cardiomyopathy is the most common primary cardiomyopathy and can cause exertional dyspnea, presyncope, atypical chest pain, heart failure, and sudden cardiac death. ...Family physicians should be alert for acquired variants of cardiomyopathy …
Hypertrophic cardiomyopathy is the most common primary cardiomyopathy and can cause exertional dyspnea, presyncope, atypical c …
Left ventricular non-compaction cardiomyopathy.
Towbin JA, Lorts A, Jefferies JL. Towbin JA, et al. Lancet. 2015 Aug 22;386(9995):813-25. doi: 10.1016/S0140-6736(14)61282-4. Epub 2015 Apr 9. Lancet. 2015. PMID: 25865865 Review.
It can be associated with left ventricular dilation or hypertrophy, systolic or diastolic dysfunction, or both, or various forms of congenital heart disease. Affected individuals are at risk of left or right ventricular failure, or both. Heart f …
It can be associated with left ventricular dilation or hypertrophy, systolic or diastolic dysfunction, or both, or various forms of c …
2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy.
Towbin JA, McKenna WJ, Abrams DJ, Ackerman MJ, Calkins H, Darrieux FCC, Daubert JP, de Chillou C, DePasquale EC, Desai MY, Estes NAM 3rd, Hua W, Indik JH, Ingles J, James CA, John RM, Judge DP, Keegan R, Krahn AD, Link MS, Marcus FI, McLeod CJ, Mestroni L, Priori SG, Saffitz JE, Sanatani S, Shimizu W, van Tintelen JP, Wilde AAM, Zareba W. Towbin JA, et al. Heart Rhythm. 2019 Nov;16(11):e301-e372. doi: 10.1016/j.hrthm.2019.05.007. Epub 2019 May 9. Heart Rhythm. 2019. PMID: 31078652
This designation includes, but is not limited to, arrhythmogenic right/left ventricular cardiomyopathy, cardiac amyloidosis, sarcoidosis, Chagas disease, and left ventricular noncompaction. The ACM phenotype overlaps with other cardiomyopathi …
This designation includes, but is not limited to, arrhythmogenic right/left ventricular cardiomyopathy, cardiac amyloid …
Pediatric Cardiomyopathies.
Lee TM, Hsu DT, Kantor P, Towbin JA, Ware SM, Colan SD, Chung WK, Jefferies JL, Rossano JW, Castleberry CD, Addonizio LJ, Lal AK, Lamour JM, Miller EM, Thrush PT, Czachor JD, Razoky H, Hill A, Lipshultz SE. Lee TM, et al. Circ Res. 2017 Sep 15;121(7):855-873. doi: 10.1161/CIRCRESAHA.116.309386. Circ Res. 2017. PMID: 28912187 Free PMC article. Review.
Pediatric cardiomyopathies are rare diseases with an annual incidence of 1.1 to 1.5 per 100 000. Dilated and hypertrophic cardiomyopathies are the most common; restrictive, noncompaction, and mixed cardiomyopathies occur infrequently; and arrhythmogeni …
Pediatric cardiomyopathies are rare diseases with an annual incidence of 1.1 to 1.5 per 100 000. Dilated and hypertrophic cardiomy …
Cardiomyopathies in children: An overview.
Tsatsopoulou A, Protonotarios I, Xylouri Z, Papagiannis I, Anastasakis A, Germanakis I, Patrianakos A, Nyktari E, Gavras C, Papadopoulos G, Meditskou S, Lazarou E, Miliou A, Lazaros G. Tsatsopoulou A, et al. Hellenic J Cardiol. 2023 Jul-Aug;72:43-56. doi: 10.1016/j.hjc.2023.02.007. Epub 2023 Mar 3. Hellenic J Cardiol. 2023. PMID: 36870438 Free article. Review.
Paediatric cardiomyopathies form a heterogeneous group of disorders characterized by structural and electrical abnormalities of the heart muscle, commonly due to a gene variant of the myocardial cell structure. ...Arrhythmogenic right ventricular ca …
Paediatric cardiomyopathies form a heterogeneous group of disorders characterized by structural and electrical abnormalities of the …
Cardiac MRI of Hereditary Cardiomyopathy.
Fadl SA, Revels JW, Rezai Gharai L, Hanneman K, Dana F, Proffitt EK, Grizzard JD. Fadl SA, et al. Radiographics. 2022 May-Jun;42(3):625-643. doi: 10.1148/rg.210147. Epub 2022 Mar 11. Radiographics. 2022. PMID: 35275782 Review.
T2*-weighted MRI is important in the detection and quantification of iron overload cardiomyopathy. Other hereditary entities for which comprehensive MRI has proven essential include Danon disease, familial dilated cardiomyopathy, hereditary muscular dystrophy, arrhy …
T2*-weighted MRI is important in the detection and quantification of iron overload cardiomyopathy. Other hereditary entities for whic …
Hypertrabeculation; a phenotype with Heterogeneous etiology.
Adabifirouzjaei F, Igata S, DeMaria AN. Adabifirouzjaei F, et al. Prog Cardiovasc Dis. 2021 Sep-Oct;68:60-69. doi: 10.1016/j.pcad.2021.07.007. Epub 2021 Jul 13. Prog Cardiovasc Dis. 2021. PMID: 34265334 Free article. Review.
Left ventricular hypertrabeculation (LVHT) is a phenotype with multiple etiologies and variable clinical presentation and significance. ...However, due to the lack of consensus diagnostic criteria, LVHT has now been reported in a broad spectrum of cardiomyopathies, …
Left ventricular hypertrabeculation (LVHT) is a phenotype with multiple etiologies and variable clinical presentation and significanc …
Cardiac Imaging In Athletes.
Khan AA, Safi L, Wood M. Khan AA, et al. Methodist Debakey Cardiovasc J. 2016 Apr-Jun;12(2):86-92. doi: 10.14797/mdcj-12-2-86. Methodist Debakey Cardiovasc J. 2016. PMID: 27486490 Free PMC article. Review.
Examples of exercise-induced changes in the heart include increases in heart cavity dimensions, augmentation of cardiac output, and increases in heart muscle mass. ...The hemodynamic effects of endurance and strength training exercise lead to these adaptation …
Examples of exercise-induced changes in the heart include increases in heart cavity dimensions, augmentation of cardiac output …
Right ventricular involvement in left ventricular non-compaction cardiomyopathy.
Stämpfli SF, Gotschy A, Kiarostami P, Özkartal T, Gruner C, Niemann M, Manka R, Tanner FC. Stämpfli SF, et al. Cardiol J. 2022;29(3):454-462. doi: 10.5603/CJ.a2020.0095. Epub 2020 Jul 10. Cardiol J. 2022. PMID: 32648250 Free PMC article.
BACKGROUND: Left ventricular non-compaction cardiomyopathy (LVNC) features extensive trabeculations. Involvement of the right ventricle (RV) has been reported; however, distinction from normal RV trabeculation is difficult. ...
BACKGROUND: Left ventricular non-compaction cardiomyopathy (LVNC) features extensive trabeculations. Involvement of the rig …
Cardiomyopathy in neurological disorders.
Finsterer J, Stöllberger C, Wahbi K. Finsterer J, et al. Cardiovasc Pathol. 2013 Sep-Oct;22(5):389-400. doi: 10.1016/j.carpath.2012.12.008. Epub 2013 Feb 22. Cardiovasc Pathol. 2013. PMID: 23433859 Review.
According to the American Heart Association, cardiomyopathies are classified as primary (solely or predominantly confined to heart muscle), secondary (those showing pathological myocardial involvement as part of a neuromuscular disorder) and those in which …
According to the American Heart Association, cardiomyopathies are classified as primary (solely or predominantly confined to …
174 results