Pia Bernardo
Overview
Explore the profile of Pia Bernardo including associated specialties, affiliations and a list of published articles.
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Articles
34
Citations
122
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Recent Articles
1.
Camillo L, Pozzi M, Bernardo P, Pisano S, Nobile M
Drug Des Devel Ther
. 2024 Nov;
18:5023-5040.
PMID: 39525048
Trofinetide is a first-in-class pharmacological treatment proposed for patients with Rett Syndrome. It is a long half-life derivative of glycine-proline-glutamate, the tripeptide normally excided from Insulin-like Growth Factor 1 upon...
2.
Onorini N, Mirone G, Cicala D, Spennato P, Rubino A, Bernardo P, et al.
World Neurosurg
. 2024 Sep;
192:127-129.
PMID: 39293735
Magnetic resonance-guided laser interstitial thermal therapy (MRgLITT) is a new minimally invasive treatment for tuberous sclerosis complex (TSC)-associated epilepsy in children. This video describes a case of a 17-year-old girl...
3.
Clara-Hwang A, Stefani S, Lau T, Scala M, Aynekin B, Bernardo P, et al.
Neurol Genet
. 2024 Jul;
10(4):e200168.
PMID: 39035822
Objectives: To present a case series of novel variants in patients presenting with genetic epileptic and developmental encephalopathy. Background: CHD2 gene encodes an ATP-dependent enzyme, chromodomain helicase DNA-binding protein 2,...
4.
Bernardo P, Scala M, Rubino A, Spennato P, Mirone G, Russo C, et al.
Epileptic Disord
. 2024 May;
26(4):460-470.
PMID: 38700931
Objective: This study aimed to evaluate epilepsy outcome and antiseizure medication (ASM) discontinuation after lesionectomies as first surgical approach in pediatric population diagnosed with low-grade epilepsy-associated neuroepithelial tumors (LEATs). Methods:...
5.
Bernardo P, Cuccurullo C, Rubino M, De Vita G, Terrone G, Bilo L, et al.
Int J Mol Sci
. 2024 Apr;
25(7).
PMID: 38612920
X-linked epilepsies are a heterogeneous group of epileptic conditions, which often overlap with X-linked intellectual disability. To date, various X-linked genes responsible for epilepsy syndromes and/or developmental and epileptic encephalopathies...
6.
Fetta A, Toni F, Pettenuzzo I, Ricci E, Rocca A, Gambi C, et al.
Orphanet J Rare Dis
. 2024 Mar;
19(1):107.
PMID: 38459574
Background: Pallister-Killian syndrome (PKS) is a rare genetic disorder caused by mosaic tetrasomy of 12p with wide neurological involvement. Intellectual disability, developmental delay, behavioral problems, epilepsy, sleep disturbances, and brain...
7.
Rubino A, Bernardo P, Russo C, Tucci C, DAmato L, Piccolo V, et al.
Brain Dev
. 2022 Sep;
45(1):87-91.
PMID: 36123197
Background: An electrical injury can cause multiple consequences, especially to the nervous system, both peripheral and central. Such consequences may present immediately as well as later on. Aims Of The...
8.
Santoro C, Mirone G, Zanobio M, Ranucci G, DAmico A, Cicala D, et al.
Int J Mol Sci
. 2022 Aug;
23(16).
PMID: 36012218
Moyamoya angiopathy (MMA) is a rare cerebral vasculopathy in some cases occurring in children. Incidence is higher in East Asia, where the heterozygous p.Arg4810Lys variant in (Mysterin) represents the major...
9.
Bernardo P, Rubino A, Santoro C, Bravaccio C, Pozzi M, Pisano S
Children (Basel)
. 2022 Jan;
9(1).
PMID: 35053647
Oculogyric crisis (OGC) represent an unusual type of dystonic movement disorder, usually reported as an adverse event of antipsychotic drugs, with acute or tardive onset, likely due to a functional...
10.
Catone G, Almerico L, Pezzella A, Riccio M, Bravaccio C, Bernardo P, et al.
Brain Sci
. 2021 Aug;
11(8).
PMID: 34439678
In youths, callous-unemotional (CU) traits and conduct problems (CP) are independently associated with bullying perpetration and these effects are also observed when controlling for sex. Moreover, research indicates that the...