| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1016/S0896-6273(00)80642-X |
| P8608 | Fatcat ID | release_y2dxmchwhbcrjibz4td7irkvye |
| P698 | PubMed publication ID | 9883716 |
| P2093 | author name string | Holmes GL | |
| Ben-Ari Y | |||
| P2860 | cites work | GABAergic cells are the major postsynaptic targets of mossy fibers in the rat hippocampus | Q28267960 |
| GABA and glutamate depolarize cortical progenitor cells and inhibit DNA synthesis | Q34400922 | ||
| Dentate granule cell neurogenesis is increased by seizures and contributes to aberrant network reorganization in the adult rat hippocampus | Q34424431 | ||
| GABAA, NMDA and AMPA receptors: a developmentally regulated 'ménage à trois'. | Q34445759 | ||
| Apoptosis and proliferation of dentate gyrus neurons after single and intermittent limbic seizures | Q36587338 | ||
| Developmental mechanisms that generate precise patterns of neuronal connectivity | Q40873406 | ||
| Phenobarbital modifies seizure-related brain injury in the developing brain | Q42284193 | ||
| Neurogenesis in neonatal rat brain is regulated by peripheral injection of basic fibroblast growth factor (bFGF). | Q42528459 | ||
| Induction of brain derived neurotrophic factor mRNA by seizures in neonatal and juvenile rat brain | Q42550771 | ||
| Infrapyramidal mossy fibers and two-way avoidance learning: developmental modification of hippocampal circuitry and adult behavior of rats and mice. | Q44900786 | ||
| Consequences of neonatal seizures in the rat: morphological and behavioral effects. | Q48330345 | ||
| Acute and chronic increases in excitability in rat hippocampal slices after perinatal hypoxia In vivo | Q48531318 | ||
| An association between granule cell density in the dentate gyrus and two-way avoidance conditioning in the house mouse | Q48708773 | ||
| Age-dependent effects of glutamate toxicity in the hippocampus | Q48827474 | ||
| Recurrent seizures in immature rats: effect on auditory and visual discrimination | Q48921069 | ||
| Developmental changes in intracellular calcium regulation in rat cerebral cortex during hypoxia. | Q51658113 | ||
| Covariations between hippocampal mossy fibres and working and reference memory in spatial and non-spatial radial maze tasks in mice. | Q52060884 | ||
| Ca2+ Oscillations Mediated by the Synergistic Excitatory Actions of GABAA and NMDA Receptors in the Neonatal Hippocampus | Q57253336 | ||
| Effect of status epilepticus on hypoxic-ischemic brain damage in the immature rat | Q71527774 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1231-1234 | |
| P577 | publication date | 1998-12-01 | |
| P1433 | published in | Neuron | Q3338676 |
| P1476 | title | Seizures in the developing brain: perhaps not so benign after all. | |
| P478 | volume | 21 |
| Q92563853 | A Screen for Synaptic Growth Mutants Reveals Mechanisms That Stabilize Synaptic Strength |
| Q44462473 | A new model for prenatal brain damage. I. GABAA receptor activation induces cell death in developing rat hippocampus |
| Q37909914 | A new neurological focus in neonatal intensive care |
| Q44462476 | A novel model for prenatal brain damage. II. Long-term deficits in hippocampal cell number and hippocampal-dependent behavior following neonatal GABAA receptor activation |
| Q35985022 | A rat model of nerve agent exposure applicable to the pediatric population: The anticonvulsant efficacies of atropine and GluK1 antagonists |
| Q36656367 | AED Treatment Through Different Ages: As Our Brains Change, Should Our Drug Choices Also? |
| Q35070078 | Age-dependent long-term structural and functional effects of early-life seizures: evidence for a hippocampal critical period influencing plasticity in adulthood |
| Q46586561 | Anticonvulsant action of GABA in the high potassium-low magnesium model of ictogenesis in the neonatal rat hippocampus in vivo and in vitro |
| Q57028097 | Assessing the Feasibility of Providing a Real-Time Response to Seizures Detected With Continuous Long-Term Neonatal Electroencephalography Monitoring |
| Q34763891 | Assessing the behavioral and cognitive effects of seizures on the developing brain |
| Q36294301 | Brain development and susceptibility to damage; ion levels and movements |
| Q35145963 | Brain plasticity in paediatric neurology |
| Q34016647 | Bumetanide, an NKCC1 antagonist, does not prevent formation of epileptogenic focus but blocks epileptic focus seizures in immature rat hippocampus |
| Q38066220 | Changing global trends in seizure outcomes following resective surgery for tuberous sclerosis in children with medically intractable epilepsy |
| Q30428208 | Clinical Seizures in Neonatal Hypoxic-Ischemic Encephalopathy Have No Independent Impact on Neurodevelopmental Outcome: Secondary Analyses of Data from the Neonatal Research Network Hypothermia Trial |
| Q35703988 | Clinical disorders of brain plasticity |
| Q45194025 | Conditional transgenic suppression of M channels in mouse brain reveals functions in neuronal excitability, resonance and behavior. |
| Q40485495 | Decrease of hippocampal GABA B receptor-mediated inhibition after hyperthermia-induced seizures in immature rats |
| Q34017315 | Decreased seizure activity in a human neonate treated with bumetanide, an inhibitor of the Na(+)-K(+)-2Cl(-) cotransporter NKCC1. |
| Q34253274 | Developing networks play a similar melody |
| Q36916620 | Developmental emergence of transient and persistent hippocampal events and oscillations and their association with infant seizure susceptibility |
| Q42572157 | Differential effects of AMPA receptor activation on survival and neurite integrity during neuronal development. |
| Q34318412 | Disruption of rolandic gamma-band functional connectivity by seizures is associated with motor impairments in children with epilepsy |
| Q36174187 | Does one neonatal seizure alter synaptic plasticity and cause lifelong cognitive impairment? |
| Q43819989 | Early development of neuronal activity in the primate hippocampus in utero. |
| Q35116253 | Early life seizures: evidence for chronic deficits linked to autism and intellectual disability across species and models |
| Q44007066 | Effect of prenatal pentylenetetrazol-induced kindling on learning and memory of male offspring |
| Q46646817 | Epileptiform activity triggers long-term plasticity of GABA(B) receptor signalling in the developing rat hippocampus |
| Q44066388 | Epileptogenesis during development: injury, circuit recruitment, and plasticity |
| Q44440504 | Estradiol Exacerbates Hippocampal Damage in a Model of Preterm Infant Brain Injury |
| Q37920349 | Ethical issues in surgical decision making concerning children with medically intractable epilepsy |
| Q40525389 | Febrile convulsions affect ultrasonic vocalizations in the rat pup. |
| Q36057730 | Febrile seizures in the developing brain result in persistent modification of neuronal excitability in limbic circuits |
| Q34094861 | Formation of heteromeric hyperpolarization-activated cyclic nucleotide-gated (HCN) channels in the hippocampus is regulated by developmental seizures |
| Q43562304 | Gamma-hydroxybutyric acid-induced absence seizures in GluR2 null mutant mice. |
| Q48158817 | Glial activation links early-life seizures and long-term neurologic dysfunction: evidence using a small molecule inhibitor of proinflammatory cytokine upregulation |
| Q35400199 | Hyper-excitability and epilepsy generated by chronic early-life stress |
| Q40575747 | Hyperthermia induces age-dependent changes in rat hippocampal excitability |
| Q44591656 | In vitro formation of a secondary epileptogenic mirror focus by interhippocampal propagation of seizures |
| Q41881245 | Invulnerability of the immature brain to seizures: do dogmas have nine lives? |
| Q36178989 | Ion channel development, spontaneous activity, and activity-dependent development in nerve and muscle cells |
| Q34763878 | Is neuronal death required for seizure-induced epileptogenesis in the immature brain? |
| Q36935512 | Living or dying in three quarter time: neonatal orchestration of hippocampal cell death pathways by androgens and excitatory GABA. |
| Q59807517 | Long-Term Effects of Early Life Seizures on Endogenous Local Network Activity of the Mouse Neocortex |
| Q30354960 | Long-term neuropathological and behavioral impairments after exposure to nerve agents |
| Q42362629 | Long-term neuroplasticity and functional consequences of single versus recurrent early-life seizures |
| Q40552011 | Long-term plasticity of endocannabinoid signaling induced by developmental febrile seizures. |
| Q34114394 | Maturation of channels and receptors: consequences for excitability |
| Q51433712 | Maturation of kainate-induced epileptiform activities in interconnected intact neonatal limbic structures in vitro. |
| Q35001724 | Mechanisms of late-onset cognitive decline after early-life stress |
| Q34094796 | Mitochondrial uncoupling protein-2 protects the immature brain from excitotoxic neuronal death. |
| Q36293677 | Models of epilepsy in the developing and adult brain: implications for neuroprotection |
| Q40467633 | Mother's Milk Protects the Immature Brain from Seizure-induced Cell Death. |
| Q44308130 | NMDA-induced seizures in developing rats cause long-term learning impairment and increased seizure susceptibility |
| Q37781440 | Neonatal Status Epilepticus |
| Q36176392 | Neonatal encephalopathy, MRI lesions, and later epilepsy: no harm, no foul? |
| Q48231376 | Neonatal seizures: characteristics of EEG ictal activity in preterm and fullterm infants |
| Q28565660 | Neural (N-) cadherin, a synaptic adhesion molecule, is induced in hippocampal mossy fiber axonal sprouts by seizure |
| Q48831416 | Pathogenesis of learning disabilities in epilepsy |
| Q34562044 | Pediatric posttraumatic seizures: epidemiology, putative mechanisms of epileptogenesis and promising investigational progress |
| Q42214350 | Persistently modified h-channels after complex febrile seizures convert the seizure-induced enhancement of inhibition to hyperexcitability |
| Q28533906 | Pregabalin attenuates excitotoxicity in diabetes |
| Q24185787 | Prophylactic barbiturate use for the prevention of morbidity and mortality following perinatal asphyxia |
| Q43540480 | Reduced neurogenesis after neonatal seizures. |
| Q36875594 | Seizure recurrence and developmental disabilities after neonatal seizures: outcomes are unrelated to use of phenobarbital prophylaxis |
| Q34572483 | Seizure suppression by gain-of-function escargot mutations |
| Q34763848 | Seizure-induced damage in the developing human: relevance of experimental models. |
| Q33165796 | Seizures and epilepsy: an overview for neuroscientists |
| Q34130234 | Seizures in extremely low birth weight infants are associated with adverse outcome. |
| Q43585716 | Surgical Treatment of Refractory Epilepsy |
| Q44781461 | Taurine as a modulator of excitatory and inhibitory neurotransmission |
| Q42100024 | Technical standards for recording and interpretation of neonatal electroencephalogram in clinical practice |
| Q44354663 | Temporal specific patterns of semaphorin gene expression in rat brain after kainic acid-induced status epilepticus. |
| Q34554344 | The clinical conundrum of neonatal seizures |
| Q24648473 | The endocannabinoid system as an emerging target of pharmacotherapy |
| Q37328931 | The epileptic hypothesis: developmentally related arguments based on animal models |
| Q48478694 | The functional significance of gap junction channels in the epileptogenicity and seizure susceptibility of juvenile rats |
| Q30707607 | The neurodevelopmental impact of childhood onset temporal lobe epilepsy on brain structure and function and the risk of progressive cognitive effects |
| Q48498785 | The neurodevelopmental impact of childhood-onset temporal lobe epilepsy on brain structure and function |
| Q51899741 | Tonic GABAergic control of mouse dentate granule cells during postnatal development |
| Q44566040 | Transition from interictal to ictal activity in limbic networks in vitro. |
| Q90625649 | Treatment of early life status epilepticus: What can we learn from animal models? |
| Q74076159 | [Neuropathologic consequences of status epilepticus] |
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