Zobrazeno 1 - 10
of 1 050
pro vyhledávání: '"Systolic anterior motion"'
Autor:
Rahul Mehrotra
Publikováno v:
Journal of the Indian Academy of Echocardiography & Cardiovascular Imaging, Vol 8, Iss 2, Pp 100-107 (2024)
Hypertrophic cardiomyopathy (HCM) is a common disorder characterized by unexplained left ventricular hypertrophy. The disease can have different phenotypic expressions and can be genetic in nature with autosomal dominant inheritance. It usually runs
Externí odkaz:
https://doaj.org/article/0993305a4c724103b3431b0794fbf4fd
Publikováno v:
Clinical Case Reports, Vol 12, Iss 1, Pp n/a-n/a (2024)
Key Clinical Message Patients with aortic valve replacement (AVR) for severe aortic stenosis (AS) will cause reversibility systolic anterior motion (SAM). This may occur because of afterload reduction caused by the relief of the AS and the prolonged
Externí odkaz:
https://doaj.org/article/7df52549728841ffb883a62690cb0612
Autor:
Pankaj Garg, Amy Lykins, Mohammad Alomari, Jordan P. Reynolds, Elizabeth Johnson, Basar Sareyyupoglu
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
BackgroundThe pulsed-electron avalanche knife (PEAK) PlasmaBlade provides an atraumatic, scalpel-like cutting precision and electrocautery-like hemostasis. PlasmaBlade operates near body temperature, and its long, thin, and malleable tip can overcome
Externí odkaz:
https://doaj.org/article/c82400fd26434ee3b4028054eae2185a
Autor:
Gaetano Todde, Grazia Canciello, Felice Borrelli, Errico Federico Perillo, Giovanni Esposito, Raffaella Lombardi, Maria Angela Losi
Publikováno v:
Cardiogenetics, Vol 13, Iss 2, Pp 75-91 (2023)
Left ventricular outflow obstruction (LVOTO) and diastolic dysfunction are the main pathophysiological characteristics of hypertrophic cardiomyopathy (HCM)LVOTO, may be identified in more than half of HCM patients and represents an important determin
Externí odkaz:
https://doaj.org/article/3e0e9ddce62e458b95a5cc898f1a3668
Publikováno v:
Indian Heart Journal, Vol 75, Iss 4, Pp 308-310 (2023)
Approximately 2/3 of patients with hypertrophic cardiomyopathy (HCM) have significant left ventricular outflow tract obstruction (LVOTO), which is caused by the interaction mitral valve apparatus and the hypertrophied septum. The contribution of mitr
Externí odkaz:
https://doaj.org/article/541c866d799842c892c2d9b6540c7231
Publikováno v:
Clinical Epidemiology and Global Health, Vol 24, Iss , Pp 101408- (2023)
Background: Myectomy is the surgical procedure for the treatment of hypertrophic cardiomyopathy (HCM) with refractory symptoms There is limited data available regarding the role of myectomy in HCM among the Indian population. This study is intended t
Externí odkaz:
https://doaj.org/article/3f6228e4e79d47e79825530d33b35cd9
Autor:
Yochun Jung, MD, PhD, Sebastian Streukens, MD, PhD, Jindrich Vainer, MD, PhD, Suzanne Kats, MD, PhD, MBA, Peyman Sardari Nia, MD, PhD
Publikováno v:
JACC: Case Reports, Vol 23, Iss , Pp 102005- (2023)
Systolic anterior motion of a mitral leaflet can occur by various mechanisms and it is one of the causes of left ventricular outflow tract obstruction after transcatheter mitral valve replacement. We present a case of systolic anterior motion that re
Externí odkaz:
https://doaj.org/article/bd36678be3af4b5a86c3f04a23946acc
Autor:
Kostiantyn V. Rudenko, Lidiia O. Nevmerzhytska, Olha M. Unitska, Polina A. Danchenko, Nadiia S. Leiko
Publikováno v:
Український журнал серцево-судинної хірургії, Vol 30, Iss 4, Pp 73-80 (2022)
Fabry disease (FD) is an X-linked lysosomal storage disease caused by a mutation in the gene encoding α-galactosidase A and leads to reduced activity or complete absence of this enzyme, which causes the accumulation of globotriaosylceramide (Gb3) an
Externí odkaz:
https://doaj.org/article/06c06706e90e48b3b302a61c91153752
Publikováno v:
Journal of Veterinary Internal Medicine, Vol 36, Iss 6, Pp 1900-1912 (2022)
Abstract Background The natural history of hypertrophic cardiomyopathy (HCM) in cats has been mainly studied in cats referred for suspected heart disease, which can skew the results towards cats with clinical signs. Few data are available on factors
Externí odkaz:
https://doaj.org/article/ca86329b307f43edac0e8441404425fb
Publikováno v:
GAIMS Journal of Medical Sciences, Vol 3, Iss 1, Pp 26-28 (2023)
Hypertrophic cardiomyopathy (HCM) is a genetic disorder characterized by left ventricular hypertrophy not explained by secondary causes, and a non-dilated left ventricle with preserved or increased ejection fraction. It is commonly asymmetric with mo
Externí odkaz:
https://doaj.org/article/2348bd851ba74440a53df92af2869ed3