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Recent related articles ( zzrr rtr d ) :
An fhl1-containing complex within the cardiomyocyte sarcomere mediates hypertrophic biomechanical stress responses in mice The response of cardiomyocytes to biomechanical stress can determine the pathophysiology of hypertrophic cardiac disease, and targeting the pathways regulating these responses is a therapeutic goal. However, little is known about how biomechanical stress is sensed by the cardiomyocyte sarcomere to transduce intracellular hypertrophic signals or how the An fhl1-containing complex within the cardiomyocyte sarcomere mediates hypertrophic biomechanical stress responses in mice ...
Therapeutic options in hypertrophic cardiomyopathy: a pediatric perspective Opinion statement Hypertrophic cardiomyopathy (HCM) is the most prevalent genetic cardiomyopathy in children and young adults. Despite advances
in understanding the molecular etiology of this disorder , the clinical phenotypes vary widely from asymptomatic septal hypertrophy,
to frank congestive heart failure due to left ventricular outflow tract obstruction (LVOTO), to Therapeutic options in hypertrophic cardiomyopathy: a pediatric perspective ...
Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in danish hypertrophic cardiomyopathy patients and relatives The American Heart Association (AHA) recommends family screening for hypertrophic cardiomyopathy (HCM). We assessed the outcome of family screening combining clinical evaluation and screening for sarcomere gene mutations in a cohort of 90 Danish HCM patients and their close relatives, in all 451 persons. Index patients were screened Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in danish hypertrophic cardiomyopathy patients and relatives ...
Successful catheter ablation of hemodynamically unstable monomorphic ventricular tachycardia in a patient with hypertrophic cardiomyopathy and apical aneurysm In this report, we describe such a patient with HCM and apical aneurysm in whom the mapping and ablation procedure was effective in identifying and abolishing the VT focus. (J Cardiovasc Electrophysiol, Vol. pp. 1[ndash]3) (Source: Journal of Cardiovascular Electrophysiology) MedWorm Sponsored Message: Find out how you can get Successful catheter ablation of hemodynamically unstable monomorphic ventricular tachycardia in a patient with hypertrophic cardiomyopathy and apical aneurysm ...
A standard echocardiographic and tissue doppler study of morphological and functional findings in children with hypertrophic cardiomyopathy compared to those with left ventricular hypertrophy in the setting of noonan and leopard syndromes Research ArticlesFabiana Cerrato, Giuseppe Pacileo, Giuseppe Limongelli, Maria Giulia Gagliardi, Giuseppe Santoro, Maria Cristina Digilio, Giovanni Di Salvo, Rachele Ardorisio, Tiziana Miele, Raffaele Calabrò, Cardiology in the Young, Volume 18 Issue 06 , pp 575-580AbstractBackground Several clinical and echocardiographic studies describe morphological and functional findings in patients with A standard echocardiographic and tissue doppler study of morphological and functional findings in children with hypertrophic cardiomyopathy compared to those with left ventricular hypertrophy in the setting of noonan and leopard syndromes ...
Mutational analysis of fukutin gene in dilated cardiomyopathy and hypertrophic cardiomyopathy. Conclusions These observations indicated that the compound heterozygous FKTN mutation was a rare cause of DCM. Hyper-CKemia might be indicative of FKTN mutation in DCM.
PMID: 19015585 [PubMed - as supplied by publisher] (Source: Circulation Journal)Mutational analysis of fukutin gene in dilated cardiomyopathy and hypertrophic cardiomyopathy. ...
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