Results 41 to 50 of about 26,229 (182)

Restrictive cardiomyopathy: difficulties desminopathy diagnostics

Российский кардиологический журнал, 2019
The article provides a brief overview of the problems of diagnostics and etiological verification of restrictive cardiomyopathy (RCMP). Multiple causes lead to the restrictive phenotype of intracardiac hemodynamics and diastolic dysfunction of the heart:
T. G. Vaikhanskaya, T. M. Kaptsiukh, T. V. Kurushko, L. N. Sivitskaya, O. D. Liaudanski, N. G. Danilenko   +5 more
doaj   +1 more source

N-terminal prohormone brain natriuretic peptide (NT-proBNP) as a noninvasive marker for restrictive syndromes [PDF]

, 2008
Constrictive pericarditis (CP) and restrictive cardiomyopathy share many similarities in both their clinical and hemodynamic characteristics and N-terminal prohormone brain natriuretic peptide (NT-proBNP) is a sensitive marker of cardiac diastolic ...
ARTEAGA, E., BUCK, P.C., FERNANDES, F., IANNI, B.M., MADY, C., NASTARI, L., RAMIRES, F.J.A., SALEMI, V.M.C.   +7 more
core   +2 more sources

Successful management of diastolic heart failure in a patient with restrictive cardiomyopathy following an anterior communicating artery aneurysm clipping

Journal of Neuroanaesthesiology and Critical Care, 2017
Perioperative management of neurosurgical patients with an underlying myocardial dysfunction poses a unique challenge to the neuroanaesthesiologist and the neurointensivist.
Rajasekar Arumugam, Georgene Singh, Krishnaprabhu Raju, Ramamani Mariappan   +3 more
doaj   +3 more sources

Genomic insights into cardiomyopathies: a comparative cross-species review [PDF]

, 2017
n the global human population, the leading cause of non-communicable death is cardiovascular disease. It is predicted that by 2030, deaths attributable to cardiovascular disease will have risen to over 20 million per year.
Beffagna, Carrier, Cruz, Elliott, Fox, Fox, Gallego-Delgado, Hilfiker-Kleiner, Huang, Inagaki, Kimura, Kucerova, Lacuata, Maekawa, Maron, Meurs, Niss, Qu, Sakamoto, Sandusky, Wang, Zeviani   +21 more
core   +1 more source

Himalayan P in a Toddler with Idiopathic Restrictive Cardiomyopathy with a Brief Electrocardiographic Review

Indian Journal of Clinical Cardiology
Although Himalayan P waves are not uncommon in congenital heart diseases involving the tricuspid valve, it is rare in pediatric idiopathic restrictive cardiomyopathy.
Sedhupathi Shanmugam, Sudipta Mondal, Saurav Banerjee   +2 more
doaj   +1 more source

Idiopathic restrictive cardiomyopathy - perspectives from genetics studies. Is it time to redefine these disorders?

Cardiogenetics, 2012
Idiopathic restrictive cardiomyopathy (IRC) is a rare form of heart muscle disease. Genetic studies have revealed that in about half the cases, IRC forms part of the hereditary sarcomeric contractile protein disease spectrum.
Ajay Bahl, Uma Nahar Saikia, Madhu Khullar   +2 more
doaj   +1 more source

Senile Systemic Amyloidosis: Clinical Features at Presentation and Outcome [PDF]

, 2013
Background Cardiac amyloidosis is a fatal disease whose prognosis and treatment rely on identification of the amyloid type. In our aging population transthyretin amyloidosis (ATTRwt) is common and must be differentiated from other amyloid types.
Banypersad, SM, Dungu, J, Gibbs, SD, Gilbertson, JA, Gillmore, JD, Hawkins, PN, Lachmann, HJ, McCarthy, CA, Petrie, A, Pinney, JH, Rowczenio, D, Sattianayagam, P, Venner, CP, Wassef, N, Wechalekar, A, Whelan, CJ   +15 more
core   +1 more source

Clinical Exome Sequencing Revealed a De Novo FLNC Mutation in a Child with Restrictive Cardiomyopathy

Cardiogenetics, 2022
Restrictive cardiomyopathy (RCM) is a rare disease of the myocardium caused by mutations in several genes including TNNT2, DES, TNNI3, MYPN and FLNC.
Francesca Girolami, Silvia Passantino, Adelaide Ballerini, Alessia Gozzini, Giulio Porcedda, Iacopo Olivotto, Silvia Favilli   +6 more
doaj   +1 more source

Sudden cardiac death in inherited cardiomyopathy [PDF]

, 2017
Cardiomyopathy is an important cause of sudden cardiac death particularly in adolescents and young adults. The risk of sudden cardiac death varies between individual cardiomyopathies and is dependent on the severity of disease, age and gender.
Collis, R, Elliott, PM
core   +1 more source

Restrictive cardiomyopathy. Presentation of seven cases

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