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1 metanide might be an effective treatment for neonatal seizures.
2 l mechanism for the early crescendo phase of neonatal seizures.
3 nic acid and flurothyl models of symptomatic neonatal seizures.
4 l and diazepam, two drugs in current use for neonatal seizures.
5 Q channels may be effective for treatment of neonatal seizures.
6 etanide should be useful in the treatment of neonatal seizures.
7 ng the diagnosis, aetiology and treatment of neonatal seizures.
8 irth weight is a significant risk factor for neonatal seizures.
9 f these infants were diagnosed with clinical neonatal seizures.
10  an add-on to phenobarbital for treatment of neonatal seizures.
11 0 minutes, meconium aspiration syndrome, and neonatal seizures, adjusted for maternal height, materna
12             There were 207 cases of clinical neonatal seizures among 116,048 live births (an incidenc
13 is study estimated the incidence of clinical neonatal seizures among infants born between 1992 and 19
14 h, an Apgar score of 3 or less at 5 minutes, neonatal seizure, an umbilical-artery blood pH of 7.05 o
15 c encephalopathy is the most common cause of neonatal seizures and can lead to chronic epilepsy.
16  In one family, the phenotype extends beyond neonatal seizures and includes rolandic seizures, and a
17 le deleterious effects of GABAergic drugs on neonatal seizures and on excitotoxic neuronal injury in
18 ng mutations responsible for benign familial neonatal seizures and/or peripheral nerve hyperexcitabil
19 re often hypotensive, needed intubation, had neonatal seizures, and received a clinical diagnosis of
20                                              Neonatal seizures are a naturally occurring source of ne
21                                      Whereas neonatal seizures are a predictor of adverse neurologica
22                                              Neonatal seizures are most commonly the clinical finding
23                                     Although neonatal seizures are quite common, there is controversy
24   This is of particular concern for treating neonatal seizures, as early life exposure to drugs such
25      Finally, human hippocampal samples from neonatal seizure autopsy cases also showed an increase i
26  known to be responsible for benign familial neonatal seizures (BFNS).
27 nt compounds inhibit motor manifestations of neonatal seizures but not cortical seizure activity.
28 ear in understanding the basis for a form of neonatal seizures can be attributed to the successful po
29                                              Neonatal seizures can lead to epilepsy and long-term cog
30                                              Neonatal seizures can lead to later life epilepsy and ne
31                                              Neonatal seizures can permanently disrupt neuronal devel
32 GABAergic) drugs, the standard treatment for neonatal seizures, can have excitatory effects in the ne
33                                              Neonatal seizures caused by hypoxia can be refractory to
34 ificates, death certificates, and a study of neonatal seizures conducted concurrently with this study
35                                              Neonatal seizures continue to present a diagnostic and t
36 nked lethal disorder involving cleft palate, neonatal seizures, contractures, central nervous system
37 nfant with ISOD who initially presented with neonatal seizures, diffusion restriction noted on magnet
38                                    Rats with neonatal seizures had a significant reduction in the num
39    Compared with controls, rats subjected to neonatal seizures had impaired learning and decreased ac
40                    Although the treatment of neonatal seizures has not significantly changed in the p
41 odent model of the most common form of human neonatal seizures, hypoxia-induced seizures (HS), we aim
42 approaches to the diagnosis and treatment of neonatal seizures, identifies some of the critical facto
43                             The incidence of neonatal seizures in Harris County was lower than the in
44 iventricular leukomalacia in the preterm and neonatal seizures in the term infant.
45 s 0-3 at 5 minutes, meconium aspiration, and neonatal seizures increased similarly with maternal BMI.
46 lifetime is found in the neonatal period and neonatal seizures lead to a propensity for epilepsy and
47                    Whether better control of neonatal seizures leads to a reduction in neurodisabilit
48 d KV 7.3, are known to cause benign familial neonatal seizures mainly by haploinsufficiency.
49                                              Neonatal seizures occur frequently, are often refractory
50 luded in the diagnostic workup of refractory neonatal seizures of unknown origin.
51 se to antidepressant exposure; the impact of neonatal seizures on dentate gyrus neurogenesis; and the
52 ted channelopathies, such as benign familial neonatal seizures or peripheral nerve hyperexcitability
53 of an unknown prior diagnosis of epilepsy or neonatal seizures) or classified as not having epilepsy
54 pothesis that neonatal encephalopathy, early neonatal seizures, or both result from early antenatal i
55 nd in children affected with benign familial neonatal seizures (R213W mutation) or with neonatal epil
56                Electroclinical uncoupling of neonatal seizures refers to electrographic seizure activ
57  [corrected] and need for resuscitation, and neonatal seizures-signs commonly attributed to birth asp
58 sted the hypothesis that a single episode of neonatal seizures (sNS) on rat postnatal day (P) 7 perma
59 recent insights about the pathophysiology of neonatal seizures that may provide the foundation for be
60      Using a rodent model of hypoxia-induced neonatal seizures that results in a persistent increase
61 eptic disorders ranging from benign familial neonatal seizures to severe epileptic encephalopathies.
62                         In a rodent model of neonatal seizures, we have shown previously that adminis
63                                 The odds for neonatal seizure were higher and the odds for admission
64                                 Infants with neonatal seizures were ascertained from four sources: ho
65                             Risk factors for neonatal seizures were evaluated in 116,048 infants born
66 ve mutation in KCNQ2 that has a phenotype of neonatal seizures without permanent clinical CNS impairm

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