نتایج جستجو برای: diabetic cardiomyopathy dcm

تعداد نتایج: 149719  

Journal: :The Tohoku journal of experimental medicine 1992
T Kanda T Yokoyama T Suzuki K Murata

We investigated abnormalities in natural killer (NK) cells in the myocardium and circulating blood of 38 patients with idiopathic dilated cardiomyopathy (DCM), 18 patients with hypertrophic cardiomyopathy, 8 patients with primary amyloidosis, and 12 age-matched normal control subjects. Immunohistochemical staining of myocardial biopsies revealed a significantly greater number of CD57-positive N...

Journal: :Journal of the American College of Cardiology 2004
Takeharu Hayashi Takuro Arimura Manatsu Itoh-Satoh Kazuo Ueda Shigeru Hohda Natsuko Inagaki Megumi Takahashi Hisae Hori Michio Yasunami Hirofumi Nishi Yoshinori Koga Hiroshi Nakamura Masunori Matsuzaki Bo Yoon Choi Sung Won Bae Cheol Woon You Kyung Hoon Han Jeong Euy Park Ralph Knöll Masahiko Hoshijima Kenneth R Chien Akinori Kimura

OBJECTIVES We sought to explore the relationship between a Tcap gene (TCAP) abnormality and cardiomyopathy. BACKGROUND Hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) cause severe heart failure and sudden death. Recent genetic investigations have revealed that mutations of genes encoding Z-disc components, including titin and muscle LIM protein (MLP), are the primary cause ...

2010
Karin Y. van Spaendonck-Zwarts Peter van Tintelen Dirk J. van Veldhuisen Walter J. Paulus

Background—Anecdotal cases of familial clustering of peripartum cardiomyopathy (PPCM) and familial occurrences of PPCM and idiopathic dilated cardiomyopathy (DCM) together have been observed, suggesting that genetic factors play a role in the pathogenesis of PPCM. We hypothesized that some cases of PPCM are part of the spectrum of familial DCM, presenting in the peripartum period. Methods and R...

2010
Karin Y. van Spaendonck-Zwarts Peter van Tintelen Dirk J. van Veldhuisen Rik van der Werf

Background—Anecdotal cases of familial clustering of peripartum cardiomyopathy (PPCM) and familial occurrences of PPCM and idiopathic dilated cardiomyopathy (DCM) together have been observed, suggesting that genetic factors play a role in the pathogenesis of PPCM. We hypothesized that some cases of PPCM are part of the spectrum of familial DCM, presenting in the peripartum period. Methods and R...

Journal: :Circulation 2010
Alban-Elouen Baruteau Erwan Donal Jean-Claude Daubert

BACKGROUND Anecdotal cases of familial clustering of peripartum cardiomyopathy (PPCM) and familial occurrences of PPCM and idiopathic dilated cardiomyopathy (DCM) together have been observed, suggesting that genetic factors play a role in the pathogenesis of PPCM. We hypothesized that some cases of PPCM are part of the spectrum of familial DCM, presenting in the peripartum period. METHODS AND...

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...

Journal: :Circulation. Cardiovascular genetics 2009
Ray E Hershberger Jose Renato Pinto Sharie B Parks Jessica D Kushner Duanxiang Li Susan Ludwigsen Jason Cowan Ana Morales Michelle S Parvatiyar James D Potter

BACKGROUND A key issue for cardiovascular genetic medicine is ascertaining if a putative mutation indeed causes dilated cardiomyopathy (DCM). This is critically important as genetic DCM, usually presenting with advanced, life-threatening disease, may be preventable with early intervention in relatives known to carry the mutation. METHODS AND RESULTS We recently undertook bidirectional reseque...

2016
Gino A. Kurian Rashmi Rajagopal Srinivasan Vedantham Mohanraj Rajesh

Oxidative and reductive stress are dual dynamic phases experienced by the cells undergoing adaptation towards endogenous or exogenous noxious stimulus. The former arises due to the imbalance between the reactive oxygen species production and antioxidant defenses, while the latter is due to the aberrant increase in the reducing equivalents. Mitochondrial malfunction is the common denominator ari...

2015
Siobhan Simpson Jennifer Edwards Thomas F. N. Ferguson-Mignan Malcolm Cobb Nigel P. Mongan Catrin S. Rutland

Cardiovascular disease is a leading cause of death in both humans and dogs. Dilated cardiomyopathy (DCM) accounts for a large number of these cases, reported to be the third most common form of cardiac disease in humans and the second most common in dogs. In human studies of DCM there are more than 50 genetic loci associated with the disease. Despite canine DCM having similar disease progressio...

Journal: :Archives of disease in childhood 2005
S M Taibjee P Ramani R Brown C Moss

There are previous reports of dilated cardiomyopathy (DCM) in recessive dystrophic epidermolysis bullosa (RDEB), a debilitating blistering skin disorder. The pathogenesis of DCM in RDEB remains uncertain, although dietary deficiency of selenium and carnitine have been implicated. A 6 year old girl with RDEB who died of DCM is reported; attention is drawn to the possible role of two potentially ...

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