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Ictal vomiting as a sign of temporal lobe epilepsy confirmed by stereo-EEG and surgical outcome.Panayiotopoulos syndrome: a clinical, EEG, and neuropsychological study of 93 consecutive patients.Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations.PCDH19-related epilepsy in two mosaic male patients.Bilateral putaminal necrosis and bronopol toxicityCharacterizing PCDH19 in human induced pluripotent stem cells (iPSCs) and iPSC-derived developing neurons: emerging role of a protein involved in controlling polarity during neurogenesis.Documentation of autonomic seizures and autonomic status epilepticus with ictal EEG in Panayiotopoulos syndrome.Epilepsy in ring 14 chromosome syndrome.Peri-ictal water drinking: a rare automatic behaviour in temporal lobe epilepsy.PCDH19-related epilepsy and Dravet Syndrome: Face-off between two early-onset epilepsies with fever sensitivity.Extending the use of stiripentol to other epileptic syndromes: a case of PCDH19-related epilepsy.A novel de novo SCN1A missense mutation in Severe Myoclonic Epilepsy Borderland.Childhood refractory focal epilepsy following acute febrile encephalopathy.Idiopathic West Syndrome followed by childhood absence epilepsy.PRRT2 is mutated in familial and non-familial benign infantile seizures.Diagnosing photosensitive epilepsy: fancy new versus old fashioned techniques in patients with different epileptic syndromes.Cognitive development in females with PCDH19 gene-related epilepsy.Epileptic seizures, movement disorders, and breathing disturbances in Rett syndrome: diagnostic relevance of video-polygraphy.Prolonged episode of dystonia and dyskinesia resembling status epilepticus following acute intrathecal baclofen withdrawal.Rolandic epilepsy: an uncommon presentation with leg motor seizures.Acute intralesional recording in hypothalamic hamartoma: description of 4 cases.Electroencephalographic features in dravet syndrome: five-year follow-up study in 22 patients.Ring 21 chromosome presenting with epilepsy and intellectual disability: clinical report and review of the literature.Mutation ofCHRNA2in a family with benign familial infantile seizures: Potential role of nicotinic acetylcholine receptor in various phenotypes of epilepsyCHD2 mutations are a rare cause of generalized epilepsy with myoclonic-atonic seizuresLacosamide in absence status epilepticusOccipital seizures induced by Intermittent Photic Stimulation in Dravet syndromePartial Trisomy 18q and Epileptic Spasms Induced by Eating Associated With Bilateral Opercular DysplasiaEpileptic encephalopathyMyoclonic astatic epilepsy: An age-dependent epileptic syndrome with favorable seizure outcome but variable cognitive evolutionIctal video-polygraphic features of perioral myoclonia with absencesChanging Times for CLN2 Disease: The Era of Enzyme Replacement Therapy
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Marina Trivisano
@ast
Marina Trivisano
@en
Marina Trivisano
@es
Marina Trivisano
@nl
Marina Trivisano
@sl
type
label
Marina Trivisano
@ast
Marina Trivisano
@en
Marina Trivisano
@es
Marina Trivisano
@nl
Marina Trivisano
@sl
prefLabel
Marina Trivisano
@ast
Marina Trivisano
@en
Marina Trivisano
@es
Marina Trivisano
@nl
Marina Trivisano
@sl
P1053
K-4692-2016
P106
P1153
36132621300
P21
P31
P3829
P496
0000-0002-9841-8581
P569
2000-01-01T00:00:00Z