The implication of coronary artery malformations and congenital heart disease on cardiomyopathy
SE Mason, SE Lipshultz, S Kaushal, S Fisher - Progress in Pediatric …, 2014 - Elsevier
Coronary and congenital heart malformations contribute to and overlap with clinical
cardiomyopathy. As cellular mechanisms and gene associations are better understood …
cardiomyopathy. As cellular mechanisms and gene associations are better understood …
Importanza dell'esame genetico in una popolazione selezionata di pazienti con cardiomiopatia dilatativa
A Carpani - 2020 - unire.unige.it
INTRODUZIONE: Solo nel 50% dei casi di cardiomiopatia dilatativa (CMD) è possibile
individuare un'eziologia specifica. Nei rimanenti casi è sempre più possibile identificare una …
individuare un'eziologia specifica. Nei rimanenti casi è sempre più possibile identificare una …
[PDF][PDF] Diagnosis and Management of Cardiomyopathies-A Focus on Genetics, Cardiac Magnetic Resonance and Clinical Features
G Sinagra, M Moretti, G Vitrella… - European …, 2011 - assets.radcliffecardiology.com
In recent years, outstanding progress has been made in the diagnosis and treatment of
cardiomyopathies. Genetics is emerging as a primary point in the diagnosis and …
cardiomyopathies. Genetics is emerging as a primary point in the diagnosis and …
[PDF][PDF] SUDDEN CARDIAC DEATH IN PEDIATRICS: GENETIC BASIS AND CLINICAL TREATMENT
G Sarquella-Brugada, O Campuzano, P Berne… - novapublishers.com
In last 15 years, cardiology has experienced an amazing progress in genetics and molecular
biology. These advances help to develop new methods of prevention, diagnosis and clinical …
biology. These advances help to develop new methods of prevention, diagnosis and clinical …
Genetische Arrhythmiesyndrome–Teil 2
BM Beckmann, A Curta, S Kääb - Kardiologie up2date, 2017 - thieme-connect.com
Hereditäre Arrhythmiesyndrome mit struktureller Herzerkrankung sind selten. Oft sind relativ
junge, ansonsten gesunde Patienten ohne kardiovaskuläre Risikofaktoren betroffen …
junge, ansonsten gesunde Patienten ohne kardiovaskuläre Risikofaktoren betroffen …
[PDF][PDF] ZBTB17 GENE SINGLE NUCLEOTIDE POLYMORPHISMS IN SLOVAK PATIENTS WITH DILATED CARDIOMYOPATHY
I Boroňová, J Bernasovská, J Kmec… - SLOVENSKÁ …, 2016 - fns.uniba.sk
Dilated cardiomyopathy (DCM) is a primary myocardial disease characterized by
progressive systolic dysfunction due to cardiac chamber dilatation and inefficient myocardial …
progressive systolic dysfunction due to cardiac chamber dilatation and inefficient myocardial …
[PDF][PDF] Targeted Next-Generation Sequencing for the Molecular Genetic Diagnostics of Cardiomyopathies
W Rottbauer - Citeseer
Background–Today mutations in more than 30 different genes have been found to cause
inherited cardiomyopathies, some associated with very poor prognosis. However, due to the …
inherited cardiomyopathies, some associated with very poor prognosis. However, due to the …
[PDF][PDF] Deputy Chief Editor: BA Sidorenko Responsible secretarial: AA Liakishev
KG Adamyan, VA Aziz, OY Atkov… - КАРДИОЛОГИЯ …, 2016 - researchgate.net
Цель—в рамках проведения открытой постмаркетинговой национальной
наблюдательной программы ВЫБОР-2 оценить соответствие между рекомендациями …
наблюдательной программы ВЫБОР-2 оценить соответствие между рекомендациями …
Risk of cardiovascular abnormalities in relatives of SUDEP victims: How should we proceed?
FA Scorza - Epilepsy & Behavior, 2015 - epilepsybehavior.com
Epilepsy is the most common serious neurological condition, and it carries a significant risk
of premature mortality that is 2-to 3-fold higher, on average, than the general population [1 …
of premature mortality that is 2-to 3-fold higher, on average, than the general population [1 …
[PDF][PDF] Homozygous SOD2 mutation as a cause of lethal neonatal dilated cardiomyopathy
R Almomani, A Posafalvi, JC Herkert… - Matters of the heart …, 2015 - research.rug.nl
Although cases are rare, neonatal and paediatric dilated cardiomyopathy (DCM) is a severe
and often lethal disease, in which a genetic factor plays an important role in disease …
and often lethal disease, in which a genetic factor plays an important role in disease …