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Quoted phrase not found in phrase index: "Dilated Cardiomyopathy, Dominant"
Page 1
Amyloidosis: prognosis and treatment.
Gertz MA, Kyle RA. Gertz MA, et al. Semin Arthritis Rheum. 1994 Oct;24(2):124-38. doi: 10.1016/s0049-0172(05)80006-x. Semin Arthritis Rheum. 1994. PMID: 7839154 Review.
The objective of this study was to review (1) the factors that have been linked to prediction of clinical outcome and survival in amyloidosis and (2) the available studies on the therapy for localized and systemic forms of amyloidosis. ...Dimethyl sulfoxide provides benefi …
The objective of this study was to review (1) the factors that have been linked to prediction of clinical outcome and survival in amy …
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy.
Barp A, Bello L, Politano L, Melacini P, Calore C, Polo A, Vianello S, Sorarù G, Semplicini C, Pantic B, Taglia A, Picillo E, Magri F, Gorni K, Messina S, Vita GL, Vita G, Comi GP, Ermani M, Calvo V, Angelini C, Hoffman EP, Pegoraro E. Barp A, et al. PLoS One. 2015 Oct 29;10(10):e0141240. doi: 10.1371/journal.pone.0141240. eCollection 2015. PLoS One. 2015. PMID: 26513582 Free PMC article.
OBJECTIVE: Dilated cardiomyopathy (DCM) is a major complication and leading cause of death in Duchenne muscular dystrophy (DMD). ...Cardiological medications were not administered before DCM onset in this population. We observed trends towards a protective effect of …
OBJECTIVE: Dilated cardiomyopathy (DCM) is a major complication and leading cause of death in Duchenne muscular dystrophy (DMD …
A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias.
Yuan F, Qiu XB, Li RG, Qu XK, Wang J, Xu YJ, Liu X, Fang WY, Yang YQ, Liao DN. Yuan F, et al. Int J Mol Med. 2015 Feb;35(2):478-86. doi: 10.3892/ijmm.2014.2029. Epub 2014 Dec 9. Int J Mol Med. 2015. PMID: 25503402 Clinical Trial.
Dilated cardiomyopathy (DCM) is the most prevalent type of primary myocardial disease, which is the third most common cause of heart failure and the most frequent reason for heart transplantation. ...As a result, a novel heterozygous NKX2-5 mutation, p.S146W, was id …
Dilated cardiomyopathy (DCM) is the most prevalent type of primary myocardial disease, which is the third most common cause of …
An updated review of implantable cardioverter/defibrillators, induced anxiety, and quality of life.
Bostwick JM, Sola CL. Bostwick JM, et al. Psychiatr Clin North Am. 2007 Dec;30(4):677-88. doi: 10.1016/j.psc.2007.07.002. Psychiatr Clin North Am. 2007. PMID: 17938040 Review.
Diagnoses as diverse as myocardial infarction in the context of advanced coronary artery disease and dilated cardiomyopathy after acute viral infection may warrant ICD placement. ...Ideally, future research would consist either of large-scale, randomized, pro …
Diagnoses as diverse as myocardial infarction in the context of advanced coronary artery disease and dilated cardiomyopathy af …
Epidemiology and genetics of dilated cardiomyopathy in the Indian context.
Ushasree B, Shivani V, Venkateshwari A, Jain RK, Narsimhan C, Nallari P. Ushasree B, et al. Indian J Med Sci. 2009 Jul;63(7):288-96. Indian J Med Sci. 2009. PMID: 19700909
BACKGROUND: Dilated cardiomyopathy (DCM) still remains to be a poorly understood and less analyzed group of cardiac-muscle disorders when compared to hypertrophic cardiomyopathy (HCM). Also, the vast clinical heterogeneity among the patients has render …
BACKGROUND: Dilated cardiomyopathy (DCM) still remains to be a poorly understood and less analyzed group of cardiac-muscle dis …
DNA analysis in inherited cardiomyopathies: current status and clinical relevance.
van Spaendonck-Zwarts KY, van den Berg MP, van Tintelen JP. van Spaendonck-Zwarts KY, et al. Pacing Clin Electrophysiol. 2008 Feb;31 Suppl 1:S46-9. doi: 10.1111/j.1540-8159.2008.00956.x. Pacing Clin Electrophysiol. 2008. PMID: 18226036 Review.
Most hypertrophic cardiomyopathies and a subset of dilated and arrhythmogenic right ventricular cardiomyopathies are familial diseases. ...Such features help target DNA testing and the results of DNA analysis can be used in making clinical decisions....
Most hypertrophic cardiomyopathies and a subset of dilated and arrhythmogenic right ventricular cardiomyopathies are familial disease …
Antisense-mediated exon skipping: a therapeutic strategy for titin-based dilated cardiomyopathy.
Gramlich M, Pane LS, Zhou Q, Chen Z, Murgia M, Schötterl S, Goedel A, Metzger K, Brade T, Parrotta E, Schaller M, Gerull B, Thierfelder L, Aartsma-Rus A, Labeit S, Atherton JJ, McGaughran J, Harvey RP, Sinnecker D, Mann M, Laugwitz KL, Gawaz MP, Moretti A. Gramlich M, et al. EMBO Mol Med. 2015 May;7(5):562-76. doi: 10.15252/emmm.201505047. EMBO Mol Med. 2015. PMID: 25759365 Free PMC article.
Frameshift mutations in the TTN gene encoding titin are a major cause for inherited forms of dilated cardiomyopathy (DCM), a heart disease characterized by ventricular dilatation, systolic dysfunction, and progressive heart failure. ...Here, we show the beneficial p …
Frameshift mutations in the TTN gene encoding titin are a major cause for inherited forms of dilated cardiomyopathy (DCM), a h …
Synthetic prostacyclin agonist, ONO1301, enhances endogenous myocardial repair in a hamster model of dilated cardiomyopathy: a promising regenerative therapy for the failing heart.
Ishimaru K, Miyagawa S, Fukushima S, Saito A, Sakai Y, Ueno T, Sawa Y. Ishimaru K, et al. J Thorac Cardiovasc Surg. 2013 Dec;146(6):1516-25. doi: 10.1016/j.jtcvs.2013.02.045. J Thorac Cardiovasc Surg. 2013. PMID: 24229503 Free article.
OBJECTIVES: Remodeling of the left ventricle (LV) in idiopathic dilated cardiomyopathy (IDCM) is known to be associated with multiple pathologic changes that endogenous factors, such as hepatocyte growth factor (HGF) and vascular endothelial growth factor (VEGF), pr …
OBJECTIVES: Remodeling of the left ventricle (LV) in idiopathic dilated cardiomyopathy (IDCM) is known to be associated with m …
Diagnosis and management of inherited cardiomyopathies.
Millar L, Sharma S. Millar L, et al. Practitioner. 2014 Oct;258(1775):21-5, 2-3. Practitioner. 2014. PMID: 25591284
Dilated cardiomyopathy (DCM) is characterised by a dilated left ventricle with impaired function that cannot be explained by ischaemic heart disease, hypertension or valvular heart disease. ...Chemotherapy and certain other drugs, alcohol abuse and myocarditi …
Dilated cardiomyopathy (DCM) is characterised by a dilated left ventricle with impaired function that cannot be explain …
Which subgroup of patients with dilated cardiomyopathy would benefit from long-term beta-blocker therapy? A histologic viewpoint.
Yamada T, Fukunami M, Ohmori M, Iwakura K, Kumagai K, Kondoh N, Minamino T, Tsujimura E, Nagareda T, Kotoh K, et al. Yamada T, et al. J Am Coll Cardiol. 1993 Mar 1;21(3):628-33. doi: 10.1016/0735-1097(93)90094-h. J Am Coll Cardiol. 1993. PMID: 8094721 Free article.
BACKGROUND: Long-term beta-blocker therapy has recently been reported to provide a favorable effect in treatment of congestive heart failure due to dilated cardiomyopathy. METHODS: Several measurements including histologic variables before administration of metoprol …
BACKGROUND: Long-term beta-blocker therapy has recently been reported to provide a favorable effect in treatment of congestive heart failure …
25 results