Bernardo Dalla Bernardina
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Explore the profile of Bernardo Dalla Bernardina including associated specialties, affiliations and a list of published articles.
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107
Citations
1806
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Recent Articles
1.
Cossu A, Furia F, Proietti J, Ancora C, Reale C, Darra F, et al.
Epilepsia
. 2024 Oct;
65(12):3595-3606.
PMID: 39463124
Objective: EEG patterns and quantitative EEG (qEEG) features have been poorly explored in monogenic epilepsies. Herein, we investigate regional differences in EEG frequency composition in patients with STXBP1 developmental and...
2.
Proietti J, Di Censo R, Spolverato S, Cossu A, Bucci A, Plebani M, et al.
Neurology
. 2024 Aug;
103(5):e209759.
PMID: 39137382
A 7-year-old right-handed girl presented to the pediatric neurology outpatient clinic after 5 episodes of headache over the previous 3 months. Her family history was positive for migraine in the...
3.
Proietti J, Fiorini E, Cantalupo G, Fontana E, Lo Barco T, Bonin C, et al.
Heliyon
. 2024 Feb;
10(2):e24747.
PMID: 38304836
In epilepsy with myoclonic-atonic seizures (EMA), status epilepticus (SE) may occur during the onset phase, uncommonly in post-puberal patients. We report a post-puberal patient with EMA who presented SE with...
4.
Specchio N, Trivisano M, Lenge M, Ferretti A, Mei D, Parrini E, et al.
Cereb Cortex
. 2023 Jul;
33(17):9709-9717.
PMID: 37429835
The clinical phenotype of Cyclin-Dependent Kinase-Like 5 (CDKL5) deficiency disorder (CDD) has been delineated but neuroimaging features have not been systematically analyzed. We studied brain magnetic resonance imaging (MRI) scans...
5.
Lenge M, Balestrini S, Mei D, Macconi L, Caligiuri M, Cuccarini V, et al.
Cereb Cortex
. 2023 Jun;
33(16):9532-9541.
PMID: 37344172
Mutations of the voltage-gated sodium channel SCN1A gene (MIM#182389) are among the most clinically relevant epilepsy-related genetic mutations and present variable phenotypes, from the milder genetic epilepsy with febrile seizures...
6.
Lo Barco T, Corona L, Solazzi R, Fiorini E, Galati G, Cossu A, et al.
Epileptic Disord
. 2023 May;
25(2):269-273.
PMID: 37194193
No abstract available.
7.
Balestrini S, Doccini V, Giometto S, Lucenteforte E, De Masi S, Giarola E, et al.
Epilepsia Open
. 2023 Mar;
8(2):517-534.
PMID: 36938796
Objectives: We describe the Residras registry, dedicated to Dravet syndrome (DS) and to other phenotypes related to SCN1A mutations, as a paradigm of registry for rare and complex epilepsies. Our...
8.
Cossu A, Santos J, Galati G, Nikanorova M, Costa P, Mang Y, et al.
Neurol Sci
. 2023 Mar;
44(6):2173-2176.
PMID: 36913149
Purpose: Heterozygous variants in PRRT2 are mostly associated with benign phenotypes, being the major genetic cause of benign familial infantile seizures (BFIS), as well as in paroxysmal disorders. We report...
9.
Darra F, Monchelato M, Loos M, Juanes M, Bernardina B, Reyes Valenzuela G, et al.
Epilepsy Res
. 2023 Feb;
190:107098.
PMID: 36739728
Objective: The study was conducted to analyze the possible diagnostic value of the electroclinical semiology of the epileptic seizures. Methods: We evaluated the medical records of 17 females and 5...
10.
Lo Barco T, Offredi F, Castino E, Proietti J, Cossu A, Fiorini E, et al.
Dev Med Child Neurol
. 2022 Nov;
65(6):838-846.
PMID: 36316303
Aim: To explore the feasibility of using an adaptive behaviour profile (ABP) assessment generated from a well-known measure-the Vineland Adaptive Behavior Scales, Second Edition (VABS-II)-as an instrument for outcome measures...