Massimo Mastrangelo
Overview
Explore the profile of Massimo Mastrangelo including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
50
Citations
567
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Furia F, Johannesen K, Bonardi C, Previtali R, Aledo-Serrano A, Mastrangelo M, et al.
Epilepsia Open
. 2024 Oct;
9(6):2186-2197.
PMID: 39361253
No abstract available.
2.
Dilena R, Molisso M, De Carli A, Mauri E, Circiello A, Di Benedetto A, et al.
Epilepsy Behav
. 2024 Aug;
159:109971.
PMID: 39094245
Objective: We aimed to evaluate epidemiology, seizure type, EEG, and etiology of neonatal seizures (NS) in a tertiary neonatal intensive care unit. Methods: Data on infants with a neurophysiological confirmation...
3.
Rosati A, LErario M, Bianchi R, Olivotto S, Battaglia D, Darra F, et al.
Epilepsia Open
. 2022 Jul;
7(3):532-540.
PMID: 35833327
Objective: To discuss the results of the KETASER01 trial and the reasons for its failure, particularly in view of future studies. Methods: KETASER01 is a multicenter, randomized, controlled, open-label, sequentially...
4.
Balagura G, Xian J, Riva A, Marchese F, Ben Zeev B, Rios L, et al.
Neurol Genet
. 2022 Jun;
8(3):e676.
PMID: 35655584
Background And Objectives: Clinical manifestations in developmental and epileptic encephalopathy (DEE) vary in severity and outcome, and the genotypic spectrum is diverse. We aim to trace the neurodevelopmental trajectories in...
5.
Minghetti S, Giorda R, Mastrangelo M, Tassi L, Zanotta N, Galbiati S, et al.
Epileptic Disord
. 2021 Nov;
24(1):176-182.
PMID: 34787083
Dynamin-1-like (DNM1L) is a gene located on chromosome 12p11.21 that encodes for dynamin-related protein (DRP1), a GTPase involved in mitochondrial and peroxisomal fusion, which plays a pivotal role in brain...
6.
Johannesen K, Liu Y, Koko M, Gjerulfsen C, Sonnenberg L, Schubert J, et al.
Brain
. 2021 Aug;
145(9):2991-3009.
PMID: 34431999
We report detailed functional analyses and genotype-phenotype correlations in 392 individuals carrying disease-causing variants in SCN8A, encoding the voltage-gated Na+ channel Nav1.6, with the aim of describing clinical phenotypes related...
7.
De Liso P, Pironi V, Mastrangelo M, Battaglia D, Craiu D, Trivisano M, et al.
Brain Sci
. 2021 Jul;
11(6).
PMID: 34207311
It has been an honor for us to receive a comment on our article "Fatal Status Epilepticus in Dravet Syndrome" [...].
8.
Raviglione F, Douzgou S, Scala M, Mingarelli A, DArrigo S, Freri E, et al.
Seizure
. 2021 Apr;
88:60-72.
PMID: 33831796
Purpose: Epilepsy is a main manifestation in the autosomal dominant mental retardation syndrome caused by heterozygous variants in MEF2C. We aimed to delineate the electro-clinical features and refine the genotype-phenotype...
9.
Dilena R, Raviglione F, Cantalupo G, Cordelli D, De Liso P, Di Capua M, et al.
Clin Neurophysiol
. 2021 Mar;
132(4):886-903.
PMID: 33684728
The aim of this work is to establish inclusive guidelines on electroencephalography (EEG) applicable to all neonatal intensive care units (NICUs). Guidelines on ideal EEG monitoring for neonates are available,...
10.
Masnada S, Pichiecchio A, Formica M, Arrigoni F, Borrelli P, Accorsi P, et al.
Neurology
. 2020 Dec;
96(9):e1319-e1333.
PMID: 33277420
Objective: Aiming to detect associations between neuroradiologic and EEG evaluations and long-term clinical outcome in order to detect possible prognostic factors, a detailed clinical and neuroimaging characterization of 67 cases...