Results 31 to 40 of about 26,269 (257)
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 +4 more
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. +3 more
core +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
Restrictive Cardiomyopathy in a Child
Pediatrics and Neonatology, 2008 Restrictive cardiomyopathy in young children is rare and carries a poor prognosis. We report an 18-month-old girl with poor feeding and abdominal distension. Except for hepatomegaly, no other gastrointestinal abnormalities were found. She had normalsized
Shan-Miao Lin +2 more
doaj +1 more source
The current state of biomarker research for Friedreich's ataxia: a report from the 2018 FARA biomarker meeting [PDF]
, 2019 The 2018 FARA Biomarker Meeting highlighted the current state of development of biomarkers for Friedreich's ataxia. A mass spectroscopy assay to sensitively measure mature frataxin (reduction of which is the root cause of disease) is being developed ...
Blair, Ian A. +8 more
core +1 more source
Exercise and hypertrophic cardiomyopathy: Two incompatible entities? [PDF]
, 2020 A greater understanding of the pathogenic mechanisms underpinning hypertrophic cardiomyopathy (HCM) has translated to improved medical care and better survival of affected individuals.
Basu, J, Malhotra, A, Papadakis, M
core +1 more source
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 +5 more
doaj +1 more source
Medicine of Ukraine, 2017 В статье рассматриваются вопросы классификации, этиологии, патогенеза, клиники, диагностики и лечения рестриктивной кардиомиопатии (РКМП) как широкого спектра заболеваний, объединенных одним патофизиологическим механизмом рестриктивной диастолической дисфункции вследствие распространенного фиброза или инфильтрации стенок желудочков различными ...
E. A. Butko, K. Yu. Kinoshenko
openaire +4 more sources
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. +7 more
core +2 more sources
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 +15 more
core +1 more source