Results 21 to 30 of about 40,890 (262)
The fundamental need for unifying phenotypes in sudden unexpected pediatric deaths
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
We aimed to study the consequences of chronic exposure to tobacco smoke in utero on the morphological and functional maturation of the brainstem by comparing stillbirths of smoker mothers versus nonsmoker mothers.
Anna Maria Lavezzi +2 more
doaj +1 more source
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
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
Genetics of Heritable Thoracic Aortic Disease
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
Background Interval duration measurements (IDMs) were compared between standard 12‐lead electrocardiograms (ECGs) and 6‐lead ECGs recorded with AliveCor's KardiaMobile 6L, a hand‐held mobile device designed for use by patients at home.
Robert Kleiman +7 more
doaj +1 more source
Factors Associated with Mothers' Knowledge about Sudden Infant Death Syndrome
Sudden Infant Death Syndrome is defined as the death of any infant under one year of age, with a sleeping position, in the prone position, being the most important risk factor.
Mariana Gabriela Anselmo +5 more
doaj +1 more source
Brugada Syndrome and GPD1L: Definite Genotype-Phenotype Association?
The GPD1L gene encodes a small cytoplasmic protein that is involved in the regulation of sodium currents. Alterations in this gene have been associated with Brugada syndrome.
Andrea Greco +10 more
doaj +1 more source

