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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
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
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
24 This is of particular concern for treating neonatal seizures, as early life exposure to drugs such
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
32 GABAergic) drugs, the standard treatment for neonatal seizures, can have excitatory effects in the ne
34 ificates, death certificates, and a study of neonatal seizures conducted concurrently with this study
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
39 Compared with controls, rats subjected to neonatal seizures had impaired learning and decreased ac
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
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
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
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
61 eptic disorders ranging from benign familial neonatal seizures to severe epileptic encephalopathies.
66 ve mutation in KCNQ2 that has a phenotype of neonatal seizures without permanent clinical CNS impairm
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