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Pia Bernardo
Observed names:
Bernardo Pia,
Bernardo, Pia,
P. Bernardo
Institution:
Santobono Children's Hospital
Observed institutions:
University of Campania "Luigi Vanvitelli",
The Francis Crick Institute,
Federico II University Hospital,
Santobono Children's Hospital,
UCL Queen Square Institute of Neurology,
University College London,
University of Naples Federico II,
University of Genoa
show all 8
ORCID:
0000-0002-4150-1624
Observed ORCID:
0000-0002-4150-1624
OpenAlex ID:
A5016228057
Epilepsy in NF1: a systematic review of the literature
2020
·
Pia Bernardo
, Giuseppe Cinalli
, et al.
·
Child s Nervous System
·
57
Seizures in children with neurofibromatosis type 1: is neurofibromatosis type 1 enough?
2018
·
Claudia Santoro
, Pia Bernardo
, et al.
·
The Italian Journal of Pediatrics/Italian journal of pediatrics
·
41
PDF
Neurophysiological Signatures of Motor Impairment in Patients with Rett Syndrome
2020
·
Pia Bernardo
, Stuart Cobb
, et al.
·
Annals of Neurology
·
28
Multiple spinal nerve enlargement and SOS1 mutation: Further evidence of overlap between neurofibromatosis type 1 and Noonan phenotype
2017
·
C. Santoro
, T. Giugliano
, et al.
·
Clinical Genetics
·
23
An Italian consensus on the management of Lennox-Gastaut syndrome
2022
·
Antonella Riva
, Antonietta Coppola
, et al.
·
Seizure
·
20
PDF
CHD2 mutations: Only epilepsy? Description of cognitive and behavioral profile in a case with a new mutation
2017
·
Pia Bernardo
, Diana Galletta
, et al.
·
Seizure
·
20
PDF
Sphingolipid Metabolism Perturbations in Rett Syndrome
2019
·
Gerarda Cappuccio
, Taraka Donti
, et al.
·
Metabolites
·
19
PDF
The Relation of Callous–Unemotional Traits and Bullying in Early Adolescence Is Independent from Sex and Age and Moderated by Conduct Problems
2021
·
Gennaro Catone
, Luisa Almerico
, et al.
·
Brain Sciences
·
17
PDF
X-Linked Epilepsies: A Narrative Review
2024
·
Pia Bernardo
, Claudia Cuccurullo
, et al.
·
International Journal of Molecular Sciences
·
15
PDF
Cognitive Profile, Emotional-Behavioral Features, and Parental Stress in Boys With 47,XYY Syndrome
2019
·
Francesca F. Operto
, Grazia M.G. Pastorino
, et al.
·
Cognitive and Behavioral Neurology
·
14
UBE2A deficiency in two siblings: A novel splicing variant inherited from a maternal germline mosaicism
2017
·
Teresa Giugliano
, Claudia Santoro
, et al.
·
American Journal of Medical Genetics Part A
·
14
Profile of Trofinetide in the Treatment of Rett Syndrome: Design, Development and Potential Place in Therapy
2024
·
Laura Camillo
, Marco Pozzi
, et al.
·
Drug Design Development and Therapy
·
13
PDF
Intrafamilial variability in SPTAN1-related disorder: From benign convulsions with mild gastroenteritis to developmental encephalopathy
2020
·
Gaetano Terrone
, Michele Pinelli
, et al.
·
European Journal of Paediatric Neurology
·
13
Vitamin D deficiency is not related to eating habits in children with Autistic Spectrum Disorder
2020
·
Maria Pia Riccio
, Gennaro Catone
, et al.
·
AIMS Public Health
·
13
Pediatric emergency care admissions for somatic symptom disorders during the COVID-19 pandemic
2022
·
R. Turco
, M. Russo
, et al.
·
European Journal of Pediatrics
·
12
PDF
Neuronal Avalanches to Study the Coordination of Large-Scale Brain Activity: Application to Rett Syndrome
2020
·
Rosaria Rucco
, Pia Bernardo
, et al.
·
Frontiers in Psychology
·
12
PDF
The Treatment of Hypersalivation in Rett Syndrome with Botulinum Toxin: Efficacy and Clinical Implications
2019
·
Pia Bernardo
, Enza Raiano
, et al.
·
Neurology and Therapy
·
12
PDF
Clinical evolution and epilepsy outcome in three patients with CDKL5‐related developmental encephalopathy
2019
·
Pia Bernardo
, Alessandro Ferretti
, et al.
·
Epileptic Disorders
·
11
PDF
Neuropsychiatric syndrome with myoclonus after SARS-CoV-2 infection in a paediatric patient
2022
·
M. Della Corte
, C. Delehaye
, et al.
·
Clinical Neurology and Neurosurgery
·
10
PDF
17q21.31 microdeletion syndrome: Description of a case further contributing to the delineation of Koolen-de Vries syndrome
2016
·
Pia Bernardo
, Francesca Madia
, et al.
·
Brain and Development
·
10
Mystery(n) Phenotypic Presentation in Europeans: Report of Three Further Novel Missense RNF213 Variants Leading to Severe Syndromic Forms of Moyamoya Angiopathy and Literature Review
2022
·
Claudia Santoro
, Giuseppe Mirone
, et al.
·
International Journal of Molecular Sciences
·
9
PDF
A novel RAB39B mutation and concurrent de novo NF1 mutation in a boy with neurofibromatosis type 1, intellectual disability, and autism: a case report
2020
·
Claudia Santoro
, Teresa Giugliano
, et al.
·
BMC Neurology
·
9
PDF
Pain and sleep disturbances in Rett syndrome and other neurodevelopmental disorders
2018
·
Gerarda Cappuccio
, Pia Bernardo
, et al.
·
Acta Paediatrica
·
9
Low‐grade epilepsy‐associated tumors: Epilepsy outcome and antiseizure medication discontinuation after lesionectomies as first‐line surgical approach in pediatric population
2024
·
Pia Bernardo
, Maria Rosaria Scala
, et al.
·
Epileptic Disorders
·
8
Aripiprazole-Induced Oculogyric Crisis: A Pediatric Case Series and A Brief Narrative Review
2021
·
Pia Bernardo
, Alfonso Rubino
, et al.
·
Children
·
8
PDF
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Works count:
54
Citation count:
467
H-index:
13
I10-index:
20
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