| P2093 | author name string | Amy Brooks-Kayal | |
| | Yogendra H Raol | |
| | Kevin E Chapman | |
| P2860 | cites work | Subunit composition at the single-cell level explains functional properties of a glutamate-gated channel | Q58051235 |
| | Incidence of Neonatal Seizures in Harris County, Texas, 1992-1994 | Q60213758 |
| | Defining the gap between electrographic seizure burden, clinical expression and staff recognition of neonatal seizures | Q63259550 |
| | The effect of acute hypoglycemia on the cerebral NMDA receptor in newborn piglets | Q71692183 |
| | NBQX blocks acute and late epileptogenic effects of perinatal hypoxia | Q71734538 |
| | The effects of hypoglycaemia on cerebral blood flow and metabolism in the new-born calf | Q72128026 |
| | A population-based study of neonatal seizures in Fayette County, Kentucky | Q72173895 |
| | Seizures accelerate anoxia-induced neuronal death in the neonatal rat hippocampus | Q73064718 |
| | Models of pediatric epilepsies: strategies and opportunities | Q80146631 |
| | EXPERIMENTAL DETERMINATION OF THE ANTICONVULSANT PROPERTIES OF SOME PHENYL DERIVATIVES | Q80932030 |
| | Cognitive function at 3 years of age after fetal exposure to antiepileptic drugs | Q24642570 |
| | The glutamate receptor ion channels | Q28137916 |
| | KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum | Q28208104 |
| | The price of innovation: new estimates of drug development costs | Q28212140 |
| | NKCC1 transporter facilitates seizures in the developing brain | Q28277258 |
| | The K+/Cl- co-transporter KCC2 renders GABA hyperpolarizing during neuronal maturation | Q28296169 |
| | Phenobarbital for febrile seizures--effects on intelligence and on seizure recurrence | Q28332044 |
| | A mouse model of tuberous sclerosis: neuronal loss of Tsc1 causes dysplastic and ectopic neurons, reduced myelination, seizure activity, and limited survival | Q28506116 |
| | Mice lacking the vitamin D receptor exhibit impaired bone formation, uterine hypoplasia and growth retardation after weaning | Q28508915 |
| | Developmental and regional expression in the rat brain and functional properties of four NMDA receptors | Q28570615 |
| | Dose translation from animal to human studies revisited | Q29618049 |
| | Synaptic assembly of the brain in the absence of neurotransmitter secretion | Q29618899 |
| | A triplet repeat expansion genetic mouse model of infantile spasms syndrome, Arx(GCG)10+7, with interneuronopathy, spasms in infancy, persistent seizures, and adult cognitive and behavioral impairment | Q30484137 |
| | A single early-life seizure impairs short-term memory but does not alter spatial learning, recognition memory, or anxiety. | Q30485578 |
| | Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous females | Q30487790 |
| | A model of symptomatic infantile spasms syndrome | Q30493207 |
| | Development of later life spontaneous seizures in a rodent model of hypoxia-induced neonatal seizures | Q30499351 |
| | Hypothermia is correlated with seizure absence in perinatal stroke | Q30537454 |
| | Abnormal vitamin B6 metabolism in alkaline phosphatase knock-out mice causes multiple abnormalities, but not the impaired bone mineralization | Q31910002 |
| | Congenital viral infections of the brain: lessons learned from lymphocytic choriomeningitis virus in the neonatal rat. | Q33308245 |
| | Epileptogenesis in the immature brain: emerging mechanisms | Q33656567 |
| | Challenges in conducting clinical trials in children: approaches for improving performance | Q33717140 |
| | The abnormal phenotypes of cartilage and bone in calcium-sensing receptor deficient mice are dependent on the actions of calcium, phosphorus, and PTH. | Q34037713 |
| | Stressed-out, or in (utero)? | Q34094868 |
| | Trends in risks associated with new drug development: success rates for investigational drugs | Q34096792 |
| | Developmental regulation of alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid receptor subunit expression in forebrain and relationship to regional susceptibility to hypoxic/ischemic injury. II. Human cerebral white matter and cortex | Q34330653 |
| | GABA and glutamate depolarize cortical progenitor cells and inhibit DNA synthesis | Q34400922 |
| | GABAA, NMDA and AMPA receptors: a developmentally regulated 'ménage à trois'. | Q34445759 |
| | Clinical Neonatal Seizures are Independently Associated with Outcome in Infants at Risk for Hypoxic-Ischemic Brain Injury | Q34457628 |
| | The role of glutamate receptor maturation in perinatal seizures and brain injury | Q34783988 |
| | A single episode of neonatal seizures permanently alters glutamatergic synapses. | Q48261425 |
| | Effect of seizures on cerebral hypoxic-ischemic lesions in immature rats | Q48271051 |
| | Postnatal development of hippocampal dentate granule cell gamma-aminobutyric acidA receptor pharmacological properties. | Q48273202 |
| | The epidemiology of clinical neonatal seizures in Newfoundland: a population-based study. | Q48310914 |
| | Effect of treatment of subclinical neonatal seizures detected with aEEG: randomized, controlled trial | Q48333649 |
| | Recurrent seizures and the molecular maturation of hippocampal and neocortical glutamatergic synapses | Q48346582 |
| | Posthemorrhagic ventricular dilation in the neonate: development and characterization of a rat model | Q48363894 |
| | Consequences of pilocarpine-induced recurrent seizures in neonatal rats | Q48410649 |
| | Kainic acid seizures in the developing brain: status epilepticus and spontaneous recurrent seizures | Q48526585 |
| | Expression of the Na-K-2Cl cotransporter is developmentally regulated in postnatal rat brains: a possible mechanism underlying GABA's excitatory role in immature brain | Q48593744 |
| | The current etiologic profile and neurodevelopmental outcome of seizures in term newborn infants | Q48595093 |
| | Comparison between simultaneously recorded amplitude integrated electroencephalogram (cerebral function monitor) and standard electroencephalogram in neonates | Q48617454 |
| | Immature mouse unilateral carotid ligation model of stroke | Q48685188 |
| | At what age is the developing cerebral cortex of the rat comparable to that of the full-term newborn human baby? | Q48695265 |
| | Development of an optimal lidocaine infusion strategy for neonatal seizures | Q48700410 |
| | Epileptogenic effect of hypoxia in the immature rodent brain | Q48712414 |
| | Whole-body hypothermia for neonates with hypoxic-ischemic encephalopathy | Q48732854 |
| | Glutamate-operated channels: developmentally early and mature forms arise by alternative splicing | Q48736461 |
| | NR2A subunit expression shortens NMDA receptor synaptic currents in developing neocortex. | Q48757604 |
| | Excitatory GABA responses in embryonic and neonatal cortical slices demonstrated by gramicidin perforated-patch recordings and calcium imaging | Q48890713 |
| | Development of amplitude-integrated electroencephalography and interburst interval in the rat. | Q48953426 |
| | Selective head cooling with mild systemic hypothermia after neonatal encephalopathy: multicentre randomised trial | Q49032647 |
| | Incidence of epilepsy and unprovoked seizures in Rochester, Minnesota: 1935-1984. | Q51052283 |
| | Giant synaptic potentials in immature rat CA3 hippocampal neurones. | Q51749893 |
| | Tetanus toxin-induced seizures in infant rats and their effects on hippocampal excitability in adulthood | Q52208914 |
| | Developmental changes in human γ‐aminobutyric acida receptor subunit composition | Q52222249 |
| | Neurologic outcome after electroencephalographically proven neonatal seizures. | Q52235764 |
| | Postnatal development of GABA-mediated synaptic inhibition in rat hippocampus. | Q52248285 |
| | Ca2+ Oscillations Mediated by the Synergistic Excitatory Actions of GABAA and NMDA Receptors in the Neonatal Hippocampus | Q57253336 |
| | Rapamycin suppresses seizures and neuronal hypertrophy in a mouse model of cortical dysplasia | Q43099344 |
| | Seizures are associated with brain injury severity in a neonatal model of hypoxia-ischemia | Q43223528 |
| | Focal brain malformations: seizures, signaling, sequencing | Q43275319 |
| | Reduced neurogenesis after neonatal seizures. | Q43540480 |
| | gamma-Aminobutyric acid(A) receptor subunit expression predicts functional changes in hippocampal dentate granule cells during postnatal development | Q43627925 |
| | Topiramate blocks perinatal hypoxia-induced seizures in rat pups | Q43738767 |
| | Prolonged seizures exacerbate perinatal hypoxic-ischemic brain damage | Q43745507 |
| | Timing of cognitive deficits following neonatal seizures: relationship to histological changes in the hippocampus | Q43806146 |
| | Spatial learning deficits without hippocampal neuronal loss in a model of early-onset epilepsy | Q43823532 |
| | Seizure-associated brain injury in term newborns with perinatal asphyxia. | Q43896003 |
| | Deletion of the mouse glycine transporter 2 results in a hyperekplexia phenotype and postnatal lethality | Q44658571 |
| | Suppression of hippocampal neurogenesis is associated with developmental stage, number of perinatal seizure episodes, and glucocorticosteroid level | Q44668508 |
| | Long-term alterations in glutamate receptor and transporter expression following early-life seizures are associated with increased seizure susceptibility | Q44693087 |
| | GABAA receptor function in developing rat thalamic reticular neurons: whole cell recordings of GABA-mediated currents and modulation by clonazepam | Q45100995 |
| | Seizures in the developing brain cause adverse long-term effects on spatial learning and anxiety | Q45168046 |
| | Conditional transgenic suppression of M channels in mouse brain reveals functions in neuronal excitability, resonance and behavior. | Q45194025 |
| | Midazolam in neonatal seizures with no response to phenobarbital | Q45309172 |
| | Inducible nitric oxide synthase and the effect of aminoguanidine in experimental neonatal meningitis. | Q46012150 |
| | Neocortical and hippocampal changes after multiple pilocarpine-induced status epilepticus in rats. | Q46460382 |
| | Kainic acid-induced status epilepticus alters GABA receptor subunit mRNA and protein expression in the developing rat hippocampus. | Q46578519 |
| | Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization. | Q46593538 |
| | Model mice for mild-form glycine encephalopathy: behavioral and biochemical characterizations and efficacy of antagonists for the glycine binding site of N-methyl D-aspartate receptor | Q46643375 |
| | Susceptibility of the developing brain to acute hypoglycemia involving A1 adenosine receptor activation | Q46693610 |
| | Dissociated gender-specific effects of recurrent seizures on GABA signaling in CA1 pyramidal neurons: role of GABA(A) receptors. | Q46755475 |
| | Increased severity of chemically induced seizures in mice with partially deleted Vitamin D receptor gene | Q46779736 |
| | Repetitive and profound insulin-induced hypoglycemia results in brain damage in newborn rats: an approach to establish an animal model of brain injury induced by neonatal hypoglycemia | Q46801412 |
| | Deletion of Pten in mouse brain causes seizures, ataxia and defects in soma size resembling Lhermitte-Duclos disease | Q47198022 |
| | Neurodevelopmental outcome in term infants with status epilepticus detected with amplitude-integrated electroencephalography | Q48087698 |
| | A novel preclinical rodent model of collagenase-induced germinal matrix/intraventricular hemorrhage. | Q48097025 |
| | The effects of epileptic cortical activity on the development of callosal projections | Q48173528 |
| | Levetiracetam for treatment of neonatal seizures | Q34860410 |
| | Talampanel suppresses the acute and chronic effects of seizures in a rodent neonatal seizure model | Q34946029 |
| | Topiramate for the treatment of neonatal seizures | Q34971508 |
| | Models for epilepsy and epileptogenesis: report from the NIH workshop, Bethesda, Maryland. | Q34992474 |
| | Electrographic seizures during therapeutic hypothermia for neonatal hypoxic-ischemic encephalopathy | Q35007565 |
| | Developmental regulation of alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid receptor subunit expression in forebrain and relationship to regional susceptibility to hypoxic/ischemic injury. I. Rodent cerebral white matter and cortex | Q35037490 |
| | Overview of the Current Animal Models for Human Seizure and Epileptic Disorders | Q35074506 |
| | Recurrent neonatal seizures result in long-term increases in neuronal network excitability in the rat neocortex. | Q35140551 |
| | Early-life seizures produce lasting alterations in the structure and function of the prefrontal cortex | Q35256963 |
| | How children's responses to drugs differ from adults | Q35827035 |
| | Neuropathogical features of a rat model for perinatal hypoxic-ischemic encephalopathy with associated epilepsy | Q36165349 |
| | Neuropathogenesis in cytomegalovirus infection: indication of the mechanisms using mouse models | Q36229534 |
| | Nonprimate models of congenital cytomegalovirus (CMV) infection: gaining insight into pathogenesis and prevention of disease in newborns | Q36359756 |
| | Animal models of germinal matrix hemorrhage | Q36562293 |
| | Targeted ablation of the vitamin D receptor: an animal model of vitamin D-dependent rickets type II with alopecia | Q36576317 |
| | Postnatal growth and morphological development of the brain: a species comparison | Q36635203 |
| | Seizures and antiepileptic drugs: does exposure alter normal brain development? | Q36698616 |
| | Effects of status epilepticus on hippocampal GABAA receptors are age-dependent. | Q36740341 |
| | Neonatal seizures: gaps between the laboratory and the clinic | Q36850252 |
| | Seizures in the developing brain: cellular and molecular mechanisms of neuronal damage, neurogenesis and cellular reorganization | Q37037979 |
| | Loss of Tsc2 in radial glia models the brain pathology of tuberous sclerosis complex in the mouse | Q37128350 |
| | A KCNQ channel opener for experimental neonatal seizures and status epilepticus | Q37151699 |
| | Neurogenesis and epilepsy in the developing brain | Q37181305 |
| | Immunotherapy with CpG oligonucleotides and antibodies to TNF-alpha rescues neonatal mice from lethal arenavirus-induced meningoencephalitis | Q37181621 |
| | Cognitive abilities and behaviour of children exposed to antiepileptic drugs in utero | Q37345777 |
| | Long-term suppression of GABAergic activity by neonatal seizures in rat somatosensory cortex. | Q37456824 |
| | Mechanisms of action, physiological effects, and complications of hypothermia | Q37523010 |
| | Using amplitude-integrated EEG in neonatal intensive care | Q37793856 |
| | What is the value of hypothermia in acute neurologic diseases and status epilepticus? | Q37941818 |
| | Phenobarbital compared with phenytoin for the treatment of neonatal seizures. | Q38499446 |
| | Ictal and interictal electrographic seizure durations in preterm and term neonates | Q38512870 |
| | Comparative aspects of the brain growth spurt | Q39707940 |
| | State of the controlled clinical trial enterprise in the United States | Q39800619 |
| | Vitamin D3 and brain development | Q40652918 |
| | Epilepsy in the developing brain: lessons from the laboratory and clinic | Q41344970 |
| | Electrographic seizures in neonates correlate with poor neurodevelopmental outcome | Q41924438 |
| | Mice lacking tissue non-specific alkaline phosphatase die from seizures due to defective metabolism of vitamin B-6. | Q42275955 |
| | Multiple pilocarpine-induced status epilepticus in developing rats: a long-term behavioral and electrophysiological study | Q42634400 |
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1857-1865 | |
| P577 | publication date | 2012-06-01 | |
| P1433 | published in | European Journal of Neuroscience | Q5412733 |
| P1476 | title | Neonatal seizures: controversies and challenges in translating new therapies from the lab to the isolette | |
| P478 | volume | 35 | |