نتایج جستجو برای: روش dcm

تعداد نتایج: 372718  

Journal: :Circulation journal : official journal of the Japanese Circulation Society 2008
Yen-Wen Wu Masanao Naya Takahiro Tsukamoto Hiroshi Komatsu Koichi Morita Keiichiro Yoshinaga Yuji Kuge Hiroyuki Tsutsui Nagara Tamaki

BACKGROUND The 11C-acetate positron emission tomography can estimate myocardial oxidative metabolism, but previous studies have only evaluated small populations and the difference between ischemic (ICM) and idiopathic dilated cardiomyopathy (DCM) has not been fully investigated. The present aims were to evaluate global and regional myocardial oxidative metabolism in a well-characterized, large ...

2018
Carolina Gil-Cayuela Ana Ortega Estefanía Tarazón Luis Martínez-Dolz Juan Cinca José Ramón González-Juanatey Francisca Lago Esther Roselló-Lletí Miguel Rivera Manuel Portolés

BACKGROUND The association between dilated cardiomyopathy (DCM) and low thyroid hormone (TH) levels has been previously described. In these patients abnormal thyroid function is significantly related to impaired left ventricular (LV) function and increased risk of death. Although TH was originally thought to be produced exclusively by the thyroid gland, we recently reported TH biosynthesis in t...

Journal: :Bosnian journal of basic medical sciences 2015
Zhengdong Guo Donghui Huang Xiange Tang Jingjing Han Jing Li

Diabetic cardiomyopathy (DCM) is one of the most severe complications of diabetes without a clear pathogenesis. Th is study investigated the adiponectin (APN) and leptin levels in type II DCM, as well as their correlation with advanced glycation end-products (AGEs). From 2011-2013, 78 type II diabetes mellitus (T2DM) cases (40-65 years old) in the Taian region were randomly selected. Based on t...

Journal: :Plant physiology 1987
W E Shafer M J Bukovac

Sorption characteristics of 2-(1-naphthyl)acetic acid (NAA), 2-(1-naphthyl)acetamide (NAAm), and 2,4-dichlorophenoxyacetic acid (2,4-D) were determined for cuticles enzymically isolated from mature tomato (Lycopersicon esculentum Mill. cv Sprinter) and pepper (Capsicum annuum L.) fruit. Sorption equilibrium for NAA and 2,4-D by tomato cuticular membranes (CM) and dewaxed cuticular membranes (DC...

Journal: :Biotechnology and bioengineering 2008
Maria A E Emanuelsson M Begoña Osuna Jan Sipma Paula M L Castro

Two up-flow fixed bed reactors (UFBR) were operated for 8 months treating a model synthetic wastewater containing 2-fluorobenzoate (2-FB) and dichloromethane (DCM). The stability of the reactors under dynamic conditions, that is, sequentially alternating pollutants (SAP), shock loads, and starvation periods was assessed. Two support materials were used: expanded clay (EC) that does not adsorb 2...

Journal: :American journal of physiology. Heart and circulatory physiology 2007
Danilo Neglia Alberto De Caterina Paolo Marraccini Andrea Natali Marco Ciardetti Cecilia Vecoli Amalia Gastaldelli Demetrio Ciociaro Paola Pellegrini Roberto Testa Luca Menichetti Antonio L'Abbate William C Stanley Fabio A Recchia

Under resting conditions, the failing heart shifts fuel use toward greater glucose and lower free fatty acid (FFA) oxidation. We hypothesized that chronic metabolic abnormalities in patients with dilated cardiomyopathy (DCM) are associated with the absence of the normal increase in myocardial glucose uptake and maintenance of cardiac mechanical efficiency in response to pacing stress. In 10 DCM...

Journal: :Circulation. Cardiovascular genetics 2011
Jeanne L Theis Katharine M Sharpe Martha E Matsumoto High Seng Chai Asha A Nair Jason D Theis Mariza de Andrade Eric D Wieben Virginia V Michels Timothy M Olson

BACKGROUND Dilated cardiomyopathy (DCM) is a heritable, genetically heterogeneous disorder that typically exhibits autosomal dominant inheritance. Genomic strategies enable discovery of novel, unsuspected molecular underpinnings of familial DCM. We performed genome-wide mapping and exome sequencing in a unique family wherein DCM segregated as an autosomal recessive (AR) trait. METHODS AND RES...

Journal: :Circulation. Cardiovascular genetics 2010
Ray E Hershberger Nadine Norton Ana Morales Duanxiang Li Jill D Siegfried Jorge Gonzalez-Quintana

BACKGROUND Rare variants in >30 genes have been shown to cause idiopathic or familial dilated cardiomyopathy (DCM), but the frequency of genetic causation remains poorly understood. We have previously resequenced 9 genes in a cohort of idiopathic or familial DCM probands for rare variants, and now we report resequencing results for 5 more genes with established relationships to DCM. METHODS A...

Journal: :Journal of the American College of Cardiology 2007
Sudhir Gupta

diopathic dilated cardiomypathy (DCM) is characterized y the progressive depression of cardiac function and left entricular dilation in the absence of coronary artery disease. here is evidence to suggest that humoral immunity plays n important role in the pathogenesis of DCM. In particlar, the role of autoantibodies in the pathogenesis of DCM as been emphasized (1). Sera from patients with DCM ...

Journal: :European journal of heart failure 2006
Michael Schupp Ulrich Kintscher Jens Fielitz Jennifer Thomas Reinhard Pregla Roland Hetzer Thomas Unger Vera Regitz-Zagrosek

BACKGROUND The peroxisome proliferator-activated receptor alpha (PPARalpha) is a central regulator of myocardial fatty acid (FA) metabolism implicated in the pathogenesis of heart failure. AIMS To characterize PPARalpha regulation in human dilated cardiomyopathy (DCM), we studied the expression of cardiac PPARalpha, cardiac carnitine palmitoyl-transferase I (CPT-1), a major PPARalpha target g...

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