46 results on '"Lortie, Anne"'
Search Results
2. Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic Lymphohistiocytosis
3. Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study
4. Brain language networks and cognitive outcomes in children with frontotemporal lobe epilepsy.
5. Rewarming affects EEG background in term newborns with hypoxic–ischemic encephalopathy undergoing therapeutic hypothermia
6. Developmental outcome after a single episode of status epilepticus
7. Clinical, environmental, and genetic determinants of multiple sclerosis in children with acute demyelination: a prospective national cohort study
8. Maturational changes of 5 Hz SSVEPs elicited by intermittent photic stimulation
9. A retrospective study on aetiology based outcome of infantile spasms
10. Pharmacogenetic testing in pediatric neurology: a pragmatic study evaluating clinician and patient perceptions.
11. The genetic landscape of infantile spasms
12. Breath acetone predicts plasma ketone bodies in children with epilepsy on a ketogenic diet
13. Hemimegalencephaly in an adult with normal intellectual function and mild epilepsy
14. Prochlorperazine in children with migraine: a look at its effectiveness and rate of akathisia
15. Novel α1 and γ2 GABAA receptor subunit mutations in families with idiopathic generalized epilepsy
16. The clinical spectrum of nodular heterotopias in children: Report of 31 patients
17. The combination of subdural and depth electrodes for intracranial EEG investigation of suspected insular (perisylvian) epilepsy
18. What is the optimal duration for vigabatrin monotherapy in patients with infantile spasms: 6 months or longer?
19. Gamma frequency SSVEP components differentiate children with febrile seizures from normal controls
20. Nonlesional Frontal Lobe Epilepsy (FLE) of Childhood: Clinical Presentation, Response to Treatment and Comorbidity
21. Infantile Spasms in Remission May Reemerge as Intractable Epileptic Spasms
22. Adult Alexander Disease With Autosomal Dominant Transmission: A Distinct Entity Caused by Mutation in the Glial Fibrillary Acid Protein Gene
23. Attention, memory, and behavioral adjustment in children with frontal lobe epilepsy
24. Deficits in executive functions and motor coordination in children with frontal lobe epilepsy
25. Characteristics of epilepsy in focal cortical dysplasia in infancy
26. Treatment of Refractory Epilepsy With MEK Inhibitor in Patients With RASopathy.
27. Periictal activity in cooled asphyxiated neonates with seizures.
28. Reye's syndrome: a reappraisal of diagnosis in 49 presumptive cases
29. Efficacy and safety of lacosamide as an adjunctive therapy for refractory focal epilepsy in paediatric patients: a retrospective single-centre study.
30. CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.
31. Novel α1 and γ2 GABAA receptor subunit mutations in families with idiopathic generalized epilepsy.
32. De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy.
33. Neonatal Seizures: Do They Damage the Brain?
34. Genetic influence on the clinical characteristics and outcome of febrile seizures—a retrospective study.
35. Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy.
36. Stroke-like episodes in autosomal recessive cytochrome oxidase deficiency.
37. The potential for increasing seizure frequency, relapse, and appearance of new seizure types with vigabatrin.
38. Optimizing the Indication of Vigabatrin in Children With Refractory Epilepsy.
39. Intellectual disability without epilepsy associated with STXBP1 disruption.
40. Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindness.
41. Seizures in Pediatric Patients With Primary Brain Tumors.
42. 2. Periictal activity in cooled asphyxiated neonates with seizures.
43. Vagus Nerve Stimulation in Pediatric Refractory Epilepsy.
44. Ataxia-Telangiectasia Presenting With a Novel Immunodeficiency
45. Mutations in DOCK7 in Individuals with Epileptic Encephalopathy and Cortical Blindness.
46. Diagnosis of Migraine in the Pediatric Emergency Department.
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