Results 21 to 30 of about 27,486 (234)

Absence of Myocardial Thyroid Hormone Inactivating Deiodinase Results in Restrictive Cardiomyopathy in Mice [PDF]

, 2012
Cardiac injury induces myocardial expression of the thyroid hormone inactivating type 3 deiodinase (D3), which in turn dampens local thyroid hormone signaling.
Antonio C. Bianco, Baudenbacher, Behzad N. Oskouei, Brooks, Carvalho-Bianco, Castillo, Cintia B. Ueta, da Rocha, Drazner, Emerson L. Olivares, Freitas, Galton, Gereben, Gordana Simovic, Hagan, Hall, Hernandez, Huang, Jose R. Pinto, Joshua M. Hare, Kinugawa, Klein, Martins, Mayrin M. Correa, Olivares, Oliveira, Peeters, Pol, Sandler, Sandler, Simonides, Simonides, Trivieri, Warner S. Simonides, Wassen, Willott   +35 more
core   +1 more source

Rhabdomyolysis in the Setting of Concomitant Use of Tafamidis, Atorvastatin, and Amiodarone

JACC: Case Reports, 2020
An 85-year-old women with transthyretin cardiac amyloidosis presented with generalized weakness, elevated liver function test levels, and creatinine kinase consistent with rhabdomyolysis 1 week after starting tafamidis.
Jessica Laird, BA, Rodney H. Falk, MD, Melissa Coyle, PharmD, CSP, Sarah A.M. Cuddy, MB BCH, BAO   +3 more
doaj   +1 more source

Improved costs and outcomes with conscious sedation vs general anesthesia in TAVR patients: Time to wake up? [PDF]

, 2017
BackgroundTranscatheter aortic valve replacement (TAVR) has become a commonplace procedure for the treatment of aortic stenosis in higher risk surgical patients.
Aksoy, Olcay, Benharash, Peyman, Fernandez, Josue, Johansen, Daniel, Kwon, Murray, Patel, Komal D, Sareh, Sohail, Satou, Nancy, Shemin, Richard J, Suh, William, Toppen, William   +10 more
core   +3 more sources

Restrictive cardiomyopathy. Report of seven cases

Acta Pediátrica de México, 2014
Restrictive cardiomyopathy is a disease characterized by ventricular diastolic failure with elevation of end-dyastolic pressure and preserved systolic function.
Fonseca Sánchez Luis Alfonso, Camacho Reyes Laura, Bobadilla Aguirre Alfredo   +2 more
doaj   +1 more source

Multimodality imaging of cor triatriatum dexter complicated with hypertrophic cardiomyopathy of restrictive phenotype

Radiology Case Reports, 2022
Cor triatriatum dexter (CTD) is an extremely rare congenital cardiac malformation in which a membrane divides the right atrium into 2 chambers. Hypertrophic cardiomyopathy (HCM) with restrictive phenotype is also a rare cardiomyopathy.
Li Liang, Min-Jie Lu, PhD
doaj   +1 more source

Molecular Characterization of Pediatric Restrictive Cardiomyopathy from Integrative Genomics [PDF]

, 2017
Pediatric restrictive cardiomyopathy (RCM) is a genetically heterogeneous heart disease with limited therapeutic options. RCM cases are largely idiopathic; however, even within families with a known genetic cause for cardiomyopathy, there is striking ...
Hinton, Robert B., Rindler, Tara N., Salomonis, Nathan, Ware, Stephanie M.   +3 more
core   +1 more source

Left Bundle Pacing for Left Bundle Branch Block and Intermittent Third-Degree Atrioventricular Block in a MYH7 Mutation-Related Hypertrophic Cardiomyopathy With Restrictive Phenotype in a Child

Frontiers in Pediatrics, 2020
Hypertrophic cardiomyopathy (HCM) is a group of myocardial diseases defined by cardiac hypertrophy which cannot be explained by secondary causes with a non-dilated left ventricle and preserved or increased ejection fraction.
Luyan Zhang, Xueying Cheng, Jinlong Chen, Ming Zhou, Tianwei Qian, Zhongman Zhang, Jie Yin, Han Zhang, Genyin Dai, Yuming Qin, Shiwei Yang   +10 more
doaj   +1 more source

Desmin-related restrictive cardiomyopathy in a pediatric patient: A case report

Indian Journal of Pathology and Microbiology, 2013
Restrictive cardiomyopathies in the pediatric population have diverse etiologies, including storage diseases like hemosiderosis, glycogenoses and desmin with its associated proteins.
Shruti Sharma, Rajnish Juneja, Gautam Sharma, Sudheer Arava, Ruma Ray   +4 more
doaj   +1 more source

Pediatric restrictive cardiomyopathy: a case report

Journal of International Medical Research, 2023
Restrictive cardiomyopathy (RCM) is a rare childhood cardiomyopathy that is a challenging diagnostic problem for clinicians. We describe a case of an 8-year-old girl with a 2-year history of shortness of breath on exertion.
Hai-Long Dai, Qing-Hui Wang, Xuan Su, Yun-Chuan Ding, Xue-Feng Guang   +4 more
doaj   +1 more source

Restrictive Cardiomyopathy: A Rare Case Report [PDF]

Al Ameen Journal of Medical Sciences, 2011
We report a 28 years old male presenting with heart failure. A thorough clinical evaluation directed us towards restrictive heart disease. Doppler echocardiographic study was used as a main modality of diagnosis and cardiac catheterization confirmed the ...
Bilal Bin Abdullah*, Mehboob.M.Kalburgi, Sahana Shetty and Satyasrinivas
doaj