Results 11 to 20 of about 7,900 (206)
The risk of epilepsy after neonatal seizures. [PDF]
Plain language summary: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.16288 This original article is commented by Nagarajan on pages 1112–1113 of this issue. Abstract Aim To estimate the cumulative risk of epilepsy after neonatal seizures and identify subpopulations at increased risk.
Tinggaard J +6 more
europepmc +2 more sources
Characteristic magnetic resonance imaging (MRI) findings in patients with chronic kernicterus are bilateral and symmetric T2-weighted hyperintensities in the globus pallidus.
Getachew Assefa Neknek, MD +3 more
doaj +1 more source
Clinicopathological Spectrum of Bilirubin Encephalopathy/Kernicterus
Bilirubin encephalopathy/kernicterus is relatively rare, but continues to occur despite universal newborn screening. What is more interesting is the spectrum of clinical and even neuropathological findings that have been reported in the literature to be ...
Sumit Das, Frank K.H. van Landeghem
doaj +1 more source
Brainstem auditory evoked responses in an equine patient population. Part II: foals. [PDF]
BackgroundReports of the use of brainstem auditory evoked response (BAER) as a diagnostic modality in foals have been limited.Hypothesis/objectivesTo describe BAER findings and associated causes of hearing loss in foals.AnimalsStudy group 18 foals (15 ...
Aleman, M +3 more
core +1 more source
Management of late-preterm and term infants with hyperbilirubinaemia in resource-constrained settings. [PDF]
Hyperbilirubinaemia is a ubiquitous transitional morbidity in the vast majority of newborns and a leading cause of hospitalisation in the first week of life worldwide.
Boo, Nem-Yun +7 more
core +2 more sources
Background: Neonatal jaundice has potentially severe side effects such as kernicterus. Prevention of kernicterus and hyperbilirubinemia is based on finding neonates with risk factors and starting treatment as soon as possible. Therefore, this study aimed
Jafar Nasiri +3 more
doaj +1 more source
Genetic Association of UGT1A1 Promoter Variants (c.-3279T>G and c.-3156G>A) with Neonatal Hyperbili-rubinemia in an Iranian Population [PDF]
Background: Several studies have reported that two promoter variants (c.-3279T>G and c.-3156G>A) in UDP-glucuronosyltransferase (UGT1A1) gene may contribute to neonatal hyperbilirubinemia.
Nasim Pouralizadeh +6 more
doaj +1 more source
The magnetic resonance images (MRI) of three children with athetotic cerebral palsy and severe neonatal jaundice were examined in the Department of Pediatric Neurology, Ohzora-no-iye Hospital and Seirei-Mikatahara General Hospital, Shizuoka, Japan.
J Gordon Millichap
doaj +1 more source
Neonatal jaundice (NJ) is common in newborn infants. Severe NJ (SNJ) has potentially negative neurological sequelae that are largely preventable in high resource settings if timely diagnosis and treatment are provided. Advancements in NJ care in low- and
Katherine M. Satrom +4 more
doaj +1 more source
Neonatal hyperbilirubinemia and Rhesus disease of the newborn: incidence and impairment estimates for 2010 at regional and global levels. [PDF]
BACKGROUND: Rhesus (Rh) disease and extreme hyperbilirubinemia (EHB) result in neonatal mortality and long-term neurodevelopmental impairment, yet there are no estimates of their burden.
Bell, Jennifer +17 more
core +2 more sources

