|3.||Hypertrophic Cardiomyopathy (Asymmetric Septal Hypertrophy)
|5.||Dilated Cardiomyopathy (Cardiomyopathy, Congestive)
|1.||Potter, James D: 7 articles (06/2011 - 09/2005)|
|2.||Pinto, Jose Renato: 6 articles (02/2015 - 10/2009)|
|3.||Parvatiyar, Michelle S: 5 articles (02/2015 - 01/2008)|
|4.||Liang, Jingsheng: 5 articles (06/2011 - 09/2005)|
|5.||Towbin, Jeffrey A: 4 articles (12/2014 - 05/2002)|
|6.||Morimoto, Sachio: 4 articles (12/2014 - 12/2005)|
|7.||Goldfarb, Lev G: 4 articles (06/2009 - 04/2005)|
|8.||Mogensen, Jens: 3 articles (11/2015 - 01/2003)|
|9.||Huang, Xupei: 3 articles (05/2015 - 09/2010)|
|10.||Metzger, Joseph M: 3 articles (09/2014 - 05/2007)|
|1.||Brain Natriuretic Peptide (Natrecor)FDA Link
08/01/2008 - "Brain (B-type) natriuretic peptide (BNP) and tissue Doppler imaging may distinguish restrictive cardiomyopathy (RCMP) from idiopathic constrictive pericardial disease (CP). "
08/01/2008 - "Comparison of usefulness of tissue Doppler imaging versus brain natriuretic peptide for differentiation of constrictive pericardial disease from restrictive cardiomyopathy."
06/07/2005 - "The efficacy of brain natriuretic peptide levels in differentiating constrictive pericarditis from restrictive cardiomyopathy."
01/01/2015 - "NT pro B type natriuretic peptide levels in constrictive pericarditis and restrictive cardiomyopathy."
04/04/2006 - "Brain natriuretic peptide levels in constrictive pericarditis and restrictive cardiomyopathy."
04/01/2001 - "Clinical and molecular studies of a large family with desmin-associated restrictive cardiomyopathy."
10/01/2015 - "The course of desmin-related restrictive cardiomyopathy (DRCM) during pregnancy has not been described previously because of the rarity of the condition. "
10/01/2013 - "Desmin-related restrictive cardiomyopathy in a pediatric patient: a case report."
12/01/2007 - "The investigation led to the diagnosis of restrictive cardiomyopathy due to desmin accumulation."
12/01/2007 - "Restrictive cardiomyopathies may have different etiologies, among which we can point out storage diseases by accumulation of different materials such as desmin. "
|3.||Amyloid (Amyloid Fibrils)IBA
05/01/2015 - "An amyloid restrictive cardiomyopathy was also present, responsible for the life-threatening conduction disturbance, but without patent cardioembolic disease. "
01/01/2009 - "Amyloid deposition in the myocardium causes restrictive cardiomyopathy. "
03/01/1999 - "Assessment of restrictive cardiomyopathy of amyloid or idiopathic etiology by magnetic resonance imaging."
01/01/1990 - "To assess left ventricular (LV) diastolic function in idiopathic restrictive cardiomyopathy (IRCM) and amyloid restrictive cardiomyopathy (ARCM), we analyzed LV cineangiograms and pressures (tip manometer) in two patients, one with IRCM and the other with ARCM. "
01/01/1990 - "Analysis of left ventricular diastolic function by the pressure-volume relation in cases with idiopathic restrictive cardiomyopathy and amyloid restrictive cardiomyopathy."
09/01/2010 - "Correcting diastolic dysfunction by Ca2+ desensitizing troponin in a transgenic mouse model of restrictive cardiomyopathy."
01/01/2010 - "Cardiac troponin mutations and restrictive cardiomyopathy."
09/03/2010 - "Cardiac diseases associated with mutations in troponin subunits include hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), and restrictive cardiomyopathy (RCM). "
01/17/2014 - "As a result of troponin-tropomyosin dysinhibition, upheld(101) hearts exhibited cardiac dysfunction and remodeling comparable to that observed during human restrictive cardiomyopathy. "
01/25/2008 - "A troponin T mutation that causes infantile restrictive cardiomyopathy increases Ca2+ sensitivity of force development and impairs the inhibitory properties of troponin."
12/01/2001 - "The Ile122 transthyretin variant associated with restrictive cardiomyopathy has been described in African-Americans and estimated to be present in approximately 4% of the Black population. "
03/01/1991 - "This individual, who died with restrictive cardiomyopathy, was found to be homozygous for this transthyretin variant and his son heterozygous for the variant. "
05/01/2006 - "Transthyretin (TTR) amyloidosis, the most common form of hereditary systemic amyloidosis, is characterized clinically by adult-onset axonal neuropathy and restrictive cardiomyopathy. "
01/01/1997 - "Transthyretin Ile 122 is a common amyloidogenic variant in African-Americans (present as a heterozygous variant in 4% of this population); therefore, the diagnosis of transthyretin Ile 122 cardiac amyloidosis should be considered in African-Americans with unexplained restrictive cardiomyopathy or arrhythmias."
03/01/2014 - "Transthyretin amyloidosis (ATTR) is either a hereditary disease related to a mutation in the transthyretin gene that leads to neuropathy and/or cardiomyopathy or an acquired disease of the elderly that leads to restrictive cardiomyopathy. "
03/01/2008 - "Because of the location of the mutation in the hinge region between the rod part and the globular head of the myosin molecule, it is possible that restrictive cardiomyopathy resulted from an impairment of flexion/extension of myosin heads during the contraction/relaxation cycle."
02/01/2008 - "Enhanced myosin performance generates a phenotype apparently analogous to that of human restrictive cardiomyopathy, possibly indicating myosin-based origins for the disease. "
09/02/2005 - "To determine whether five mutations in cTnI (L144Q, R145W, A171T, K178E, and R192H) associated with restrictive cardiomyopathy were distinguishable from hypertrophic cardiomyopathy-causing mutations in cTnI, actomyosin ATPase activity and skinned fiber studies were carried out. "
11/01/2004 - "Dystrophic cardiac calcinosis, an age-related cardiomyopathy, is associated with elevated bone resorption markers and it may cause alterations in cellular calcium hemostasis with initiation of deleterious events leading to aggravate dilated and restrictive cardiomyopathy and may result in intractable congestive heart failure. "
05/01/2015 - "Calcium desensitizer catechin reverses diastolic dysfunction in mice with restrictive cardiomyopathy."
05/01/2015 - "The present study investigates the effect of the green tea extract catechins on myofibril calcium desensitization and restoration of diastolic function in a restrictive cardiomyopathy (RCM) mouse model with cardiac troponin mutations. "
09/02/2005 - "Mutations in human cardiac troponin I that are associated with restrictive cardiomyopathy affect basal ATPase activity and the calcium sensitivity of force development."
|8.||tranilast (N 5')IBA
03/01/2010 - "Genetic analyses excluded familial CA. All patients (AL-lambda (n = 22), AL-kappa (n = 3), senile amyloidosis (n = 5)) had echocardiographic signs of restrictive cardiomyopathy (RCM), typical TDI and strain parameters (E'septal; E' lateral < 8 cm/s; E/E' > 8; S' < or =9 cm/s; global longitudinal strain (GLS) -7.9 +/- 3.8%). "
03/01/2005 - "Real-time cine MRI studies, using the steady-state free precession (SSFP) technique, were performed in the cardiac short-axis during operator-guided deep inspiration and expiration in normal volunteers (N = 6), and in patients with constrictive pericarditis (CP; N = 6), restrictive cardiomyopathy (RCM; N = 4), chronic cor pulmonale (N = 5), and pericardial effusion. "
10/01/2006 - "In 50 reported cases, LVHT has been overlooked and misdiagnosed as dilated (n = 20), hypertrophic (n = 14) or restrictive cardiomyopathy (n = 2), endocardial fibroelastosis (n = 5), endomyocardial fibrosis (n = 1), myocarditis (n = 3), thrombus (n = 2), localised left ventricular hypertrophy (n = 1), left ventricular mass (n = 1) or myocardial/pericardial disease (n = 1). "
|9.||Methionine (L-Methionine)FDA Link
09/06/1999 - "The aims of the study were to identify carriers and non-carriers of the mutant transthyretin methionine 111 linked familial amyloid disease, to detect early signs of the restrictive cardiomyopathy and other clinical manifestations of this disease. "
05/01/1998 - "To identify carriers and non-carriers of the mutant transthyretin methionine 111 linked familial amyloid disease, to detect early signs of the restrictive cardiomyopathy and other clinical manifestations characteristic of this inheritable disease. "
04/01/1998 - "The purpose of this study was to analyze the subpopulation of collagen fibers and determine the expression of matrix metalloproteinase in restrictive cardiomyopathy. "
04/01/1998 - "The matrix metalloproteinase appeared to be involved in a cascade of collagen synthesis and the remodeling of the heart in patients with restrictive cardiomyopathy."
04/01/1998 - "Collagen subtypes and matrix metalloproteinase in idiopathic restrictive cardiomyopathy."
01/01/1986 - "Besides elastic and collagen fibres, numerous smooth muscle (SM) cells were found in the thickened endocardium in 3 cases of restrictive cardiomyopathy and in 1 case of congenital endocardial fibroelastosis. "
04/01/1998 - "In endomyocardial biopsy specimens obtained from seven patients with restrictive cardiomyopathy, collagen fiber types I, III, and IV, and matrix metalloproteinase- and two were observed by light and electron microscopy, using monoclonal antibodies. "
01/01/2011 - "A comprehensive evaluation by noninvasive and invasive studies facilitated the differentiation of CP from restrictive cardiomyopathy and the patient was effectively treated with pericardectomy. "
07/01/1994 - "A diagnosis of restrictive cardiomyopathy was arrived at in 4 instances, always after pericardiectomy. "
01/01/2005 - "Whereas constrictive pericarditis has the potential of being cured with pericardiectomy, restrictive cardiomyopathy is usually incurable. "
05/01/2013 - "The aim of our study was to compare myocardial mechanics of constrictive pericarditis (CP) with restrictive cardiomyopathy (RCM), or healthy controls; to assess the impact of pericardial thickening detected by cardiac magnetic resonance on regional myocardial mechanics in CP; and to quantitate the effect of pericardiectomy on myocardial mechanics in CP. "
05/01/2013 - "Biventricular mechanics in constrictive pericarditis comparison with restrictive cardiomyopathy and impact of pericardiectomy."
11/01/1990 - "Thoracotomy continues, however, to be the gold standard by which to make the distinction, carrying with it significant risk in patients with underlying restrictive cardiomyopathy."
08/01/1999 - "Notoriously difficult to diagnose and distinguish from restrictive cardiomyopathy (RCM), the use of cardiac catheterization, echocardiography (transthoracic and transesophageal), central venous (hepatic and pulmonary) and transvalvular Doppler measurements, and magnetic resonance imaging should secure the diagnosis in most cases, eliminating the need for diagnostic thoracotomy. "
05/01/1987 - "It identifies a large subset of patients with specific forms of restrictive cardiomyopathy in whom thoracotomy should be avoided. "
05/01/1987 - "Restrictive cardiomyopathy versus constrictive pericarditis: role of endomyocardial biopsy in avoiding unnecessary thoracotomy."
12/01/1980 - "A restrictive cardiomyopathy, which developed in the patient described in this report, was due to hemochromatosis which mimicked constrictive pericarditis clinically, echocardiographically and hemodynamically, and resulted in a thoracotomy for attempted surgical therapy. "
12/01/2009 - "Outcomes of children with restrictive cardiomyopathy listed for heart transplant: a multi-institutional study."
11/01/2014 - "No patient with restrictive cardiomyopathy survived; 1 patient (13%) in ECPR group after late cardiac graft failure survived to discharge. "
01/18/2013 - "failed or burned-out transplants, infiltrative and restrictive cardiomyopathies and failed ventricular assist devices. "
05/01/2012 - "Restrictive Cardiomyopathy is managed either conservatively or cardiac transplant may be offered. "
10/01/2011 - "A 9-year-old boy with restrictive cardiomyopathy, a PA pressure of 85/53 mmHg, received a HHT because he would probably not be able to tolerate an orthotopic heart transplant secondary to elevated PA pressure. "
|4.||Heart Transplantation (Grafting, Heart)
10/01/2014 - "[Myocardial changes in heart transplantation recipients with primary restrictive cardiomyopathy]."
05/01/2013 - "Pediatric heart transplantation for congenital and restrictive cardiomyopathy."
12/01/2012 - "Outcomes of adults with restrictive cardiomyopathy after heart transplantation."
01/01/2012 - "A teenage boy with endstage restrictive cardiomyopathy underwent the first heart transplantation with a pediatric donor heart in Japan on April 12, 2011. "
01/01/2008 - "Twenty-year experience with heart transplantation for infants and children with restrictive cardiomyopathy: 1986-2006."
|5.||Transplantation (Transplant Recipients)
09/01/2005 - "Without transplantation, most children with restrictive cardiomyopathy have a very poor prognosis. "
04/01/2002 - "The mean age of diagnosis of restrictive cardiomyopathy was 6.3 years and the mean interval from diagnosis to referral for transplantation was 3.6 years. "
04/01/2002 - "We reviewed our experience with the presentation, evaluation, and short-term outcome in 8 pediatric patients with restrictive cardiomyopathy referred for transplantation. "
04/01/2002 - "Because of the poor prognosis of pediatric restrictive cardiomyopathy, transplantation has been proposed as the treatment of choice for this disease. "
01/01/2001 - "One patient required transplantation at 40 months for restrictive cardiomyopathy. "