Results 91 to 100 of about 4,105 (205)

Magnetic resonance imaging of the brain in children with chronic kernicterus

open access: yes, 2006
Advances in perinatal monitoring and early treatment for hyperbilirubinemia in high-risk patients have greatly reduced the incidence of kernicterus. Findings on MRI in patients with kernicterus are characteristic.
Atalar, Mehmet H.   +2 more
core  

Promoterless gene targeting without nucleases rescues lethality of a Crigler‐Najjar syndrome mouse model

open access: yesEMBO Molecular Medicine, 2017
Crigler‐Najjar syndrome type I (CNSI) is a rare monogenic disease characterized by severe neonatal unconjugated hyperbilirubinemia with a lifelong risk of neurological damage and death. Liver transplantation is the only curative option, which has several
Fabiola Porro   +8 more
doaj   +1 more source

Hyperintense globus pallidus on T1-weighted MR imaging in acute kernicterus: is it common or rare?

open access: yes, 2005
Globus pallidus involvement is a well-known magnetic resonance (MR) imaging finding of acute kernicterus. However, it is not clear how early the involvement of globus pallidus occurs and whether or not it is seen in every case.
Kumandas, Sefer   +11 more
core   +1 more source

Kernicterus and Prematurity [PDF]

open access: yesArchives of Disease in Childhood, 1955
V M, CROSSE, T C, MEYER, J W, GERRARD
openaire   +2 more sources

Kernicterus by glucose-6-phosphate dehydrogenase deficiency: a case report and review of the literature-0

open access: yes, 2011
Copyright information:Taken from "Kernicterus by glucose-6-phosphate dehydrogenase deficiency: a case report and review of the literature"http://www.jmedicalcasereports.com/content/2/1/146Journal of Medical Case Reports 2008;2():146-146.Published online ...
Rosalío Ramos-Payán (92165)   +7 more
core   +1 more source

Kernicterus by glucose-6-phosphate dehydrogenase deficiency: a case report and review of the literature

open access: yes, 2008
Introduction Glucose-6-phosphate dehydrogenase deficiency is an X-linked recessive disease that causes acute or chronic hemolytic anemia and potentially leads to severe jaundice in response to oxidative agents.
Gerardo Vaca Pacheco   +15 more
core   +1 more source

Short Term Development and Fate of MGE-Like Neural Progenitor Cells in Jaundiced and Non-Jaundiced Rat Brain

open access: yesCell Transplantation, 2018
Neonatal hyperbilirubinemia targets specific brain regions and can lead to kernicterus. One of the most debilitating symptoms of kernicterus is dystonia, which results from bilirubin toxicity to the globus pallidus (GP).
Fu-Chen Yang   +5 more
doaj   +1 more source

Bilirubin Triggers Calcium Elevations and Dysregulates Giant Depolarizing Potentials During Rat Hippocampus Maturation

open access: yesCells
Neonatal hyperbilirubinemia may result in long-lasting motor, auditory and learning impairments. The mechanisms responsible for the localization of unconjugated bilirubin (UCB) to specific brain areas as well as those involved in potentially permanent ...
Giada Cellot   +5 more
doaj   +1 more source

Kernicterus bij een aterm geboren jongen van enkele dagen oud

open access: yes, 2002
A male baby born at term via an uncomplicated vaginal delivery was presented on the fourth day of life with jaundice, accompanied by neurological symptoms related to kernicterus. Despite extensive investigations, a clear cause for his hyperbilirubinaemia
Van Der Knaap, M. S.   +3 more
core  

New Autopsy Findings in Different Brain Regions of a Preterm Neonate With Kernicterus: Neurovascular Alterations and Up-regulation of Efflux Transporters

open access: yes, 2013
Kernicterus is an irreversible brain damage caused by bilirubin deposition in selective brain regions. Sick and preterm infants with hyperbilirubinemia are particularly susceptible to the condition.
Brito, Maria A.   +4 more
core   +1 more source

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