Results 101 to 110 of about 1,241,202 (345)

Behavioral and epileptic phenotypes in a CHD2‐related developmental delay model

Epilepsia, EarlyView.
Abstract Objective Heterozygous loss‐of‐function mutations in the CHD2 gene, encoding chromodomain helicase DNA‐binding protein 2, are associated with severe childhood onset epilepsy, global developmental delay, and autistic features. Animal models that accurately recapitulate human phenotypes are crucial for understanding rare neurodevelopmental ...
Anat Mavashov, Shaked Turk, Yael Sarusi, Marina Brusel, Rotem Ben Tov Perry, Shir Quinn, Yael Almog, Karni Vilian, Mor Yam, Igor Ulitsky, Moran Rubinstein   +10 more
wiley   +1 more source

Educational animation about home care with premature newborn infants [PDF]

, 2018
Thais da Rocha Cicero Pinto, Denise Silveira de Castro, Maria Edla de Oliveira Bringuente, Hugo Cristo Sant’Anna, Tânia Vignuda de Souza, Cândida Çaniçali Primo   +5 more
openalex   +1 more source

THE PROBLEM OF THE PREMATURE INFANT [PDF]

BMJ, 1902
openaire   +3 more sources

Epilepsy syndromes classification

Epilepsia 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, Nicola Specchio, Rima Nabbout, Phillip L. Pearl, Kate Riney   +4 more
wiley   +1 more source

Behavioral state and the premature’s readiness performance to begin oral feeding

Revista CEFAC
Objective: to evaluate the influence of behavioral states on the readiness of the premature infant to initiate breastfeeding. Methods: the study was transversal, observational and descriptive with 51 premature infants, attended at the Neonatal Intensive
Cristina Ide Fujinaga, Sabrina Maltauro, Suzelaine Taize Stadler, Eleidiele Rosa Cheffer, Sidelisa Aguiar, Nelma Ellen Zamberlan Amorin, Cleomara Mocelin Salla   +6 more
doaj   +1 more source

Genetic epilepsies with myoclonic seizures: Mechanisms and syndromes

Epilepsia Open, EarlyView.
Abstract Genetic epilepsy with myoclonic seizures encompasses a heterogeneous spectrum of conditions, ranging from benign and self‐limiting forms to severe, progressive disorders. While their causes are diverse, a significant proportion stems from genetic abnormalities.
Antonietta Coppola, Marica Rubino, Antonella Riva, Pasquale Striano   +3 more
wiley   +1 more source

Maternal risk factors associated with the birth of preterm infants in the West of Iran: a matched case-control study

BMC Pregnancy and Childbirth
Background Preterm birth is one of the global most common causes of mortality among infants, especially in developing countries. Therefore, the present study was conducted to determine the maternal risk factors related to the birth of preterm infants ...
Leila Jafarpour, Nasrin Galehdar, Yaser Mokhayeri, Kowsar Qaderi, Mahmood Fakhri   +4 more
doaj   +1 more source

Detecting bursts in the EEG of very and extremely premature infants using a multi-feature approach

, 2017
John M. O’Toole, Geraldine B. Boylan, Rhodri O. Lloyd, Robert M. Goulding, Sampsa Vanhatalo, Nathan J. Stevenson   +5 more
openalex   +1 more source

Digestion of Human Milk Oligosaccharides by Bifidobacterium breve in the Premature Infant

Journal of Pediatric Gastroenterology and Nutrition - JPGN, 2017
M. Underwood, Jasmine C C Davis, K. Kalanetra, S. Gehlot, S. Patole, D. Tancredi, D. Mills, C. Lebrilla, K. Simmer   +8 more
semanticscholar   +1 more source

Precision therapies for genetic epilepsies in 2025: Promises and pitfalls

Epilepsia Open, EarlyView.
Abstract By targeting the underlying etiology, precision therapies offer an exciting paradigm shift to improve the stagnant outcomes of drug‐resistant epilepsies, including developmental and epileptic encephalopathies. Unlike conventional antiseizure medications (ASMs) which only treat the symptoms (seizures) but have no effect on the underlying ...
Shuyu Wang, Emilio Perucca, Samuel F. Berkovic, Piero Perucca   +3 more
wiley   +1 more source