Giuseppe Gobbi
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Explore the profile of Giuseppe Gobbi including associated specialties, affiliations and a list of published articles.
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70
Citations
831
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Recent Articles
1.
Mercante A, Pizza F, Pondrelli F, Zini A, Cirillo L, Tinuper P, et al.
Clin Med Insights Pediatr
. 2024 Sep;
18:11795565241249596.
PMID: 39281040
Stretch syncope (SS) is a benign, uncommon, distinct condition described mainly in adolescent males. It is responsible for paroxysmal events started by stereotyped stretching actions with neck hyperextension, culminating in...
2.
Riva A, Coppola A, Bisulli F, Verrotti A, Bagnasco I, Elia M, et al.
Epilepsia Open
. 2024 Aug;
9(5):1857-1867.
PMID: 39176980
Objective: Rare and complex epilepsies encompass a diverse range of disorders characterized by seizures. We aimed to establish a consensus on key issues related to these conditions through collaboration among...
3.
Coppola A, Krithika S, Iacomino M, Bobbili D, Balestrini S, Bagnasco I, et al.
Epilepsia
. 2023 Dec;
65(3):779-791.
PMID: 38088023
Objective: Epilepsy with eyelid myoclonia (EEM) spectrum is a generalized form of epilepsy characterized by eyelid myoclonia with or without absences, eye closure-induced seizures with electroencephalographic paroxysms, and photosensitivity. Based...
4.
Rossi J, Russo M, Gobbi G, Terracciano A, Zuntini R, Caraffi S, et al.
Brain Dev
. 2023 Jun;
45(8):445-450.
PMID: 37271660
Introduction: Raynaud-Claes syndrome is a very rare X-linked condition, characterized by intellectual disability, impaired language development, brain abnormalities, facial dysmorphisms and drug-resistant epilepsy. It is caused by loss-of-function variants in...
5.
Castriota F, Gobbi G, Squeri A, Nerla R
J Invasive Cardiol
. 2022 Dec;
34(12):E884.
PMID: 36476821
To the best of our knowledge, this is the first report of simultaneous grasping of the 3 leaflets during TriClip (Abbott Cardiovascular) implantation. The final valve configuration with a triple...
6.
Riva A, Coppola A, Di Bonaventura C, Elia M, Ferlazzo E, Gobbi G, et al.
Seizure
. 2022 Aug;
101:134-140.
PMID: 35981474
Purpose: Although international guidelines exist, the clinical heterogeneity of Lennox-Gastaut syndrome (LGS) and the increasing availability of new and repurposed drugs (e.g., fenfluramine and cannabidiol) requires a practical guide to...
7.
Russo A, Cuteri V, Bansal L, Bonanni P, Danieli A, Pini A, et al.
Iran J Child Neurol
. 2021 Nov;
15(4):95-104.
PMID: 34782846
Objectives: To analyze the efficacy and safety of Brivaracetam in pediatric patients with epileptic encephalopathy or unresponsive focal epilepsy. Materials & Methods: This retrospective study included eight pediatric patients with...
8.
Russo A, Francione S, Martinoni M, Zucchelli M, Guerra A, Terrone G, et al.
Epileptic Disord
. 2021 Sep;
23(5):775-785.
PMID: 34519651
We describe a patient with focal epilepsy characterized by ictal asystole episodes and low-grade tumour over the left temporal neocortex. Non-invasive pre-surgical evaluation showed an epileptogenic zone extended beyond the...
9.
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...
10.
Malerba F, Alberini G, Balagura G, Marchese F, Amadori E, Riva A, et al.
Neurol Genet
. 2021 Mar;
6(6):e528.
PMID: 33659638
Objective: Early identification of de novo variants in patients with epilepsy raises prognostic issues toward optimal management. We analyzed the clinical and genetic information from a cohort of patients with...