Results 81 to 90 of about 153,464 (290)

SIDS and infant sleeping position : audit on the advisory campaign in Malta [PDF]

open access: yes, 2008
Background: The baby’s sleeping position is the most important modifiable risk factor in Sudden Infant Death Syndrome (SIDS). The “back to sleep” position is safer than side or prone position.
Attard Montalto, Simon   +2 more
core  

The Laryngeal Auditory Startle Reflex (LASR): A New Component of the Auditory Startle Response

open access: yesThe Laryngoscope, EarlyView.
The auditory startle reflex contains a distinct laryngeal component, termed the laryngeal auditory startle reflex (LASR). In healthy adults, the LASR is modulated by supratentorial influences and habituates to repetitive stimuli. Physiologic and pathologic implications for the LASR as a component of the overall human SR remain to be determined but may ...
Catherine F. Sinclair   +4 more
wiley   +1 more source

Sudden Infant Death Syndrome and Left Ventricular Hypertrabeculation-Hidden Arrhythmogenic Entity?

open access: yesClinical Medicine Insights: Cardiology, 2010
Left ventricular noncompaction/hypertrabeculation is a condition which is characterized by a highly trabeculated, “spongy” myocardium. It can present at any age with heart failure, arrhythmia and/or thromboembolic events. A wide variety of mutations have
G. Saayman   +3 more
doaj   +2 more sources

SUDDEN CHILDREN DEATH SYNDROME (SCDS) AS WELL AS SUDDEN INFANT DEATH SYNDROME (SIDS)

open access: yesМать и дитя в Кузбассе, 2018
The review gives the definition for the syndrome of sudden (and unexpected) death in children (including infants), its prevalence, likely causes and mechanisms of development.
Юрий Иванович Ровда   +3 more
doaj  

Review of nutrition management of pediatric intestinal pseudo‐obstruction

open access: yesNutrition in Clinical Practice, EarlyView.
Abstract Chronic intestinal pseudo‐obstruction (CIPO) is a rare, heterogeneous, and debilitating disorder characterized by profound intestinal dysmotility and severe nutrition challenges. Its presentation resembles that of mechanical bowel obstruction, but CIPO occurs in the absence of luminal obstruction.
Senthilkumar Sankararaman   +5 more
wiley   +1 more source

The Association of Pregnancy and Scurvy in Indigenous Women and Their Children From the Late Holocene in California (USA)

open access: yesInternational Journal of Osteoarchaeology, EarlyView.
ABSTRACT Limited evidence of nutritional deficiencies has been identified in bioarchaeological studies of Native California populations, although isotopic and ethnohistoric research provides evidence of regional, seasonal, and cultural variability in food shortages.
Alyson Caine   +3 more
wiley   +1 more source

Yield of Whole Genome Sequencing for Pathogenic Single Nucleotide Variants in Congenital Heart Disease: A Systematic Review and Meta‐Analysis

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objective This systematic review and meta‐analysis aimed to assess the diagnostic yield of pathogenic or likely pathogenic (P/LP) single nucleotide variants (SNVs) using whole genome sequencing (WGS) in congenital heart disease (CHD). Methods A systematic search of three databases (2000–2024) was conducted, and two reviewers independently ...
Hiba J. Mustafa   +7 more
wiley   +1 more source

Possible role of SCN4A skeletal muscle mutation in apnea during seizure

open access: yesEpilepsia Open, 2019
SCN4A gene mutations cause a number of neuromuscular phenotypes including myotonia. A subset of infants with myotonia‐causing mutations experience severe life‐threatening episodic laryngospasm with apnea.
Dilşad Türkdoğan   +8 more
doaj   +1 more source

KIDS COUNT Indicator Brief: Reducing Infant Mortality [PDF]

open access: yes, 2009
Examines U.S. infant mortality trends by race/ethnicity and among industrialized nations. Outlines strategies to improve women's health, ensure timely prenatal care, address racial/ethnic disparities, and continue prevention efforts past the first ...
Barbara Shore, Rima Shore
core  

Jervell and Lange‐Nielsen Syndrome Related Clinical Genetics and Experimental Models

open access: yesPediatric Discovery, EarlyView.
ABSTRACT Jervell and Lange‐Nielsen syndrome (JLNS) is defined by electrocardiographic QT prolongation and sensorineural hearing loss, caused by homozygous or compound heterozygous variants in KCNQ1 and/or KCNE1. KCNQ1 encodes the alpha subunit Kv7.1 of the ion channels accountable for slow delayed rectifier potassium currents (IKs), whereas KCNE1 ...
Yafei Zhou   +3 more
wiley   +1 more source

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