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Elena Gardella
Elena Gardella
Associate Professor, University of Southern Denmark
Dirección de correo verificada de filadelfia.dk
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Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
M Wolff, KM Johannesen, UBS Hedrich, S Masnada, G Rubboli, ...
Brain 140 (5), 1316-1336, 2017
5142017
Salzburg consensus criteria for non-convulsive status epilepticus–approach to clinical application
M Leitinger, S Beniczky, A Rohracher, E Gardella, G Kalss, E Qerama, ...
Epilepsy & Behavior 49, 158-163, 2015
4182015
Encephalopathy with electrical status epilepticus during slow sleep or ESES syndrome including the acquired aphasia
CA Tassinari, G Rubboli, L Volpi, S Meletti, G d'Orsi, M Franca, ...
Clinical Neurophysiology 111, S94-S102, 2000
3772000
The phenotypic spectrum of SCN8A encephalopathy
J Larsen, GL Carvill, E Gardella, G Kluger, G Schmiedel, N Barisic, ...
Neurology 84 (5), 480-489, 2015
2872015
Diagnostic accuracy of the Salzburg EEG criteria for non-convulsive status epilepticus: a retrospective study
M Leitinger, E Trinka, E Gardella, A Rohracher, G Kalss, E Qerama, ...
The Lancet Neurology 15 (10), 1054-1062, 2016
2702016
Central pattern generators for a common semiology in fronto-limbic seizures and in parasomnias. A neuroethologic approach
CA Tassinari, G Rubboli, E Gardella, G Cantalupo, G Calandra-Buonaura, ...
Neurological Sciences 26, s225-s232, 2005
2652005
Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation
E Gardella, F Becker, RS Møller, J Schubert, JR Lemke, LHG Larsen, ...
Annals of neurology 79 (3), 428-436, 2016
1852016
Mutations in KCNT1 cause a spectrum of focal epilepsies
RS Møller, SE Heron, LHG Larsen, CX Lim, MG Ricos, MA Bayly, ...
Epilepsia 56 (9), e114-e120, 2015
1582015
Phenotypic spectrum of GABRA1 From generalized epilepsies to severe epileptic encephalopathies
K Johannesen, C Marini, S Pfeffer, RS Møller, T Dorn, CE Niturad, ...
Neurology 87 (11), 1140-1151, 2016
1452016
The phenotype of SCN8A developmental and epileptic encephalopathy
E Gardella, C Marini, M Trivisano, MP Fitzgerald, M Alber, KB Howell, ...
Neurology 91 (12), e1112-e1124, 2018
1432018
Clinical spectrum and genotype–phenotype associations of KCNA2-related encephalopathies
S Masnada, UBS Hedrich, E Gardella, J Schubert, C Kaiwar, EW Klee, ...
Brain 140 (9), 2337-2354, 2017
1372017
Epilepsy with myoclonic absences
CA Tassinari, M Bureau, P Thomas
Epileptic syndromes in infancy, childhood and adolescence 2, 151-160, 1992
1321992
Defining the phenotypic spectrum of SLC6A1 mutations
KM Johannesen, E Gardella, T Linnankivi, C Courage, A de Saint Martin, ...
Epilepsia 59 (2), 389-402, 2018
1212018
Neuroethological approach to frontolimbic epileptic seizures and parasomnias: the same central pattern generators for the same behaviours
CA Tassinari, G Cantalupo, B Högl, P Cortelli, L Tassi, S Francione, ...
Revue neurologique 165 (10), 762-768, 2009
1202009
Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease
S Zagaglia, C Selch, JR Nisevic, D Mei, Z Michalak, ...
Neurology 91 (22), e2078-e2088, 2018
1132018
Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability
Y Liu, J Schubert, L Sonnenberg, KL Helbig, CE Hoei-Hansen, M Koko, ...
Brain 142 (2), 376-390, 2019
1072019
Standardized computer-based organized reporting of EEG: SCORE–second version
S Beniczky, H Aurlien, JC Brøgger, LJ Hirsch, DL Schomer, E Trinka, ...
Clinical Neurophysiology 128 (11), 2334-2346, 2017
1062017
Phenotypic and genetic spectrum of SCN8A‐related disorders, treatment options, and outcomes
E Gardella, RS Møller
Epilepsia 60, S77-S85, 2019
892019
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications
KM Johannesen, Y Liu, M Koko, CE Gjerulfsen, L Sonnenberg, J Schubert, ...
Brain 145 (9), 2991-3009, 2022
862022
Patients with epilepsy and patients with psychogenic non-epileptic seizures: video-EEG, clinical and neuropsychological evaluation
K Turner, A Piazzini, V Chiesa, V Barbieri, A Vignoli, E Gardella, G Tisi, ...
Seizure 20 (9), 706-710, 2011
862011
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Artículos 1–20