Results 21 to 30 of about 855,287 (330)
Inherited Arrhythmogenic Syndromes
Cardiogenetics, 2023 Inherited arrhythmogenic syndromes (IASs) are a heterogeneous group of rare cardiac entities of genetic origin [...]
Georgia Sarquella-Brugada +1 more
doaj +1 more source
The role of sodium channels in sudden unexpected death in pediatrics
Molecular Genetics & Genomic Medicine, 2020 Background Sudden Unexpected Death in Pediatrics (SUDP) is a tragic event, likely caused by the complex interaction of multiple factors. The presence of hippocampal abnormalities in many children with SUDP suggests that epilepsy‐related mechanisms may ...
Anne M. Rochtus +7 more
doaj +1 more source
Clinical course of patients with hypertrophic cardiomyopathy away from tertiary referral care
ESC Heart Failure, 2023 Aims Data on the clinical course of hypertrophic cardiomyopathy (HCM) are mainly derived from tertiary HCM centre studies, and knowledge of clinical outcomes of patients leaving specialty care and returning to local physicians is limited due to gaps ...
Ramin Garmany +4 more
doaj +1 more source
The fundamental need for unifying phenotypes in sudden unexpected pediatric deaths
Frontiers in Medicine, 2023 A definitive, authoritative approach to evaluate the causes of unexpected, and ultimately unexplained, pediatric deaths remains elusive, relegating final conclusions to diagnoses of exclusion in the vast majority of cases.
Monica H. Wojcik +15 more
doaj +1 more source
Frontiers in Pediatrics, 2016 Crib death, or sudden infant death syndrome (SIDS), is the most frequent form of death in the first year of life, striking one baby in every 1,700–2,000.
Giulia Ottaviani
doaj +1 more source
Entanglement sudden death and sudden birth in two uncoupled spins [PDF]
, 2009 We investigate the entanglement evolution of two qubits interacting with a common environment trough an Heisenberg XX mechanism. We reveal the possibility of realizing the phenomenon of entanglement sudden death as well as the entanglement sudden birth ...
A Messina +5 more
core +1 more source
Scientific Reports, 2023 Hypertrophic cardiomyopathy (HCM) is a genetically heterogenous condition with about half of cases remaining genetically elusive or non-genetic in origin.
Ramin Garmany +10 more
doaj +1 more source
The Cerebellum and SIDS: Disordered Breathing in a Mouse Model of Developmental Cerebellar Purkinje Cell Loss during Recovery from Hypercarbia. [PDF]
, 2016 The cerebellum assists coordination of somatomotor, respiratory, and autonomic actions. Purkinje cell alterations or loss appear in sudden infant death and sudden death in epilepsy victims, possibly contributing to the fatal event. We evaluated breathing
Calton, Michele A +4 more
core +2 more sources
Genetics of Heritable Thoracic Aortic Disease
Cardiogenetics, 2022 Genetic testing plays an increasing diagnostic and prognostic role in the management of patients with heritable thoracic aortic disease (HTAD). The identification of a specific variant can establish or confirm the diagnosis of syndromic HTAD, dictate ...
Efstathios Papatheodorou +2 more
doaj +1 more source