Giuliana Messina
Overview
Explore the profile of Giuliana Messina including associated specialties, affiliations and a list of published articles.
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Articles
10
Citations
23
Followers
0
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Recent Articles
1.
Filareto I, Mosca I, Freri E, Ragona F, Canafoglia L, Solazzi R, et al.
Front Cell Neurosci
. 2025 Feb;
18:1512365.
PMID: 39926415
Variants in genes encoding for voltage-gated K (Kv) channels are frequent cause of drug-resistant pediatric epilepsies. Obtaining a molecular diagnosis gives the opportunity to assess the efficacy of pharmacological strategies...
2.
Castellotti B, Gellera C, Caputo D, Danti F, Messina G, Corbetta M, et al.
Mov Disord
. 2024 Oct;
39(12):2300-2302.
PMID: 39404500
No abstract available.
3.
Castellotti B, Ragona F, Freri E, Messina G, Magri S, Previtali R, et al.
Epilepsia Open
. 2024 Aug;
9(5):1922-1930.
PMID: 39215763
Objective: The objective of this study is to report the results of the genetic analysis in a large and well-characterized population with pediatric-onset epilepsies and to identify those who could...
4.
Mosca I, Freri E, Ambrosino P, Belperio G, Granata T, Canafoglia L, et al.
Front Cell Neurosci
. 2024 Apr;
18:1367838.
PMID: 38644974
Variants in are associated with a wide spectrum of epileptic phenotypes, including epilepsy of infancy with migrating focal seizures (EIMFS), non-EIMFS developmental and epileptic encephalopathies, autosomal dominant or sporadic sleep-related...
5.
DiFrancesco J, Ragona F, Murano C, Frosio A, Melgari D, Binda A, et al.
Epilepsia
. 2023 Sep;
64(12):e222-e228.
PMID: 37746765
Missense variants of hyperpolarization-activated, cyclic nucleotide-gated (HCN) ion channels cause variable phenotypes, ranging from mild generalized epilepsy to developmental and epileptic encephalopathy (DEE). Although variants of HCN1 are an established...
6.
Ambrosino P, Ragona F, Mosca I, Vannicola C, Canafoglia L, Solazzi R, et al.
Epilepsia
. 2023 May;
64(7):e148-e155.
PMID: 37203213
Variable phenotypes, including developmental encephalopathy with (DEE) or without seizures and myoclonic epilepsy and ataxia due to potassium channel mutation, are caused by pathogenetic variants in KCNC1, encoding for Kv3.1...
7.
Castellotti B, Canafoglia L, Freri E, Tappata M, Messina G, Magri S, et al.
Epilepsia Open
. 2023 Jan;
8(2):645-650.
PMID: 36719163
Variants of SEMA6B have been identified in an increasing number of patients, often presenting with progressive myoclonus epilepsy (PME), and to lesser extent developmental encephalopathy, with or without epilepsy. The...
8.
Solazzi R, Castellotti B, Canafoglia L, Messina G, Magri S, Freri E, et al.
Epileptic Disord
. 2021 Jul;
23(4):643-647.
PMID: 34259158
Pathogenic variants in the SCN8A gene have been associated with a broad phenotypic spectrum, ranging from benign familial infantile seizures to severe, early-onset developmental and epileptic encephalopathy. This spectrum also...
9.
Freri E, Castellotti B, Canafoglia L, Ragona F, Solazzi R, Vannicola C, et al.
Seizure
. 2021 Apr;
88:143-145.
PMID: 33895390
No abstract available.
10.
Canafoglia L, Franceschetti S, Granata T, Messina G, Solazzi R, Ragona F, et al.
Seizure
. 2020 Oct;
82:56-58.
PMID: 33007625
No abstract available.