Results 41 to 50 of about 3,843,610 (234)

Establishing consensus diagnostic criteria for ring chromosome 20 syndrome: A modified electronic Delphi consensus study

open access: yesEpilepsia, EarlyView.
Abstract Objective This study was undertaken to establish expert consensus clinical and diagnostic criteria for ring chromosome 20 syndrome using a modified electronic Delphi process. Methods In this modified two‐round electronic Delphi consensus study, international experts rated candidate statements using a 9‐point Likert scale.
Abizairie Sánchez‐Feliciano   +15 more
wiley   +1 more source

Sudden infant death syndrome: an unrecognized killer in developing countries [PDF]

open access: yes, 2016
Ikenna Kingsley Ndu Department of Paediatrics, Enugu State University Teaching Hospital, Enugu, Nigeria Abstract: Sudden infant death syndrome (SIDS) is defined as the sudden unexpected death of an infant <1 year of age, with onset of the fatal ...
Ndu IK
core  

Sudden infant death syndrome: are we any closer to identifying which infants will be affected?

open access: yesPediatric Health, Medicine and Therapeutics, 2013
Tara L Ramirez, Michael H MalloyDepartment of Pediatrics, The University of Texas Medical Branch, Galveston, TX, USAAbstract: Sudden infant death syndrome is a complex and multifactoral process.
Ramirez TL, Malloy MH
doaj  

Comparative assessment of artificial intelligence chatbots' performance in responding to healthcare professionals' and caregivers' questions about Dravet syndrome

open access: yesEpilepsia Open, EarlyView.
Abstract Objective Artificial intelligence chatbots have been a game changer in healthcare, providing immediate, round‐the‐clock assistance. However, their accuracy across specific medical domains remains under‐evaluated. Dravet syndrome remains one of the most challenging epileptic encephalopathies, with new data continuously emerging in the ...
Joana Jesus‐Ribeiro   +4 more
wiley   +1 more source

Epilepsy syndromes classification

open access: yesEpilepsia Open, EarlyView.
Abstract Epilepsy syndromes are distinct electroclinical entities which have been recently defined by the International League Against Epilepsy Nosology and Definitions Task Force. Each syndrome is associated with “a characteristic cluster of clinical and EEG features, often supported by specific etiologic findings”.
Elaine C. Wirrell   +4 more
wiley   +1 more source

Knowledge of Mothers About Risk Factors Related to Sudden Infant Death Syndrome [PDF]

open access: yes
Objective: Sudden infant death syndrome (SIDS) is unexpected and unexplained sudden death of infants under one year of age. Sleep-related infant deaths can be reduced with the safe sleep environment recommendations of the American Academy of Pediatrics ...
Aybüke YAZICI, Betül SİYAH BİLGİN
core   +1 more source

New insights into epileptic spasm generation and treatment from the TTX animal model

open access: yesEpilepsia Open, EarlyView.
Abstract Currently, we have an incomplete understanding of the mechanisms underlying infantile epileptic spasms syndrome (IESS). However, over the past decade, significant efforts have been made to develop IESS animal models to provide much‐needed mechanistic information for therapy development.
John W. Swann   +2 more
wiley   +1 more source

Sudden Infant Death Syndrome: A Case Report in Pakistan [PDF]

open access: yes, 2019
Sudden infant death syndrome (SIDS) is the sudden death of an infant without any identified cause after a complete autopsy report, death scene investigation and from parent’s history.
Sehar, Sana   +2 more
core  

The role of respiratory failure caused by congenital central nervous system abnormalities and the effect of β-casomorphins in sudden infant death syndrome pathogenesis

open access: yes, 2015
The aim of the paper is to discuss the role of respiratory failure caused by endogenous (both structural and functional) abnormalities in the central nervous system and exogenous food-derived opioid-like peptides in the pathogenesis of sudden infant ...
Tomasz Gos   +2 more
core   +1 more source

Genetic developmental and epileptic encephalopathies in adulthood: Gaps in evidence and care

open access: yesEpilepsia Open, EarlyView.
Abstract Developmental and epileptic encephalopathies (DEEs) are a heterogeneous group of the most severe epilepsies, characterized by seizure onset and neurodevelopmental delay in infancy or childhood, often with additional neurological and systemic comorbidities.
Alex M. Dudley   +5 more
wiley   +1 more source

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