Roberto Gaggero
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Explore the profile of Roberto Gaggero including associated specialties, affiliations and a list of published articles.
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17
Citations
205
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Recent Articles
1.
Lenci G, Calevo M, Gaggero R, Prato G, Pisciotta L, De Grandis E, et al.
Brain Dev
. 2019 Feb;
41(6):522-530.
PMID: 30797668
Introduction: Epilepsy with continuous spike-waves during slow sleep syndrome (CSWSS) is characterized by various seizure types, a characteristic EEG pattern and neuropsychological disorders. The main purpose of this study was...
2.
Gaggero R, Pistorio A, Pignatelli S, Rossi A, Mancardi M, Baglietto M, et al.
Eur J Paediatr Neurol
. 2014 Mar;
18(3):376-80.
PMID: 24589195
Purposes: To evaluate the possibility of early syndrome classification of idiopathic partial epilepsies in children at the first seizure. Patients And Methods: In this observational study we prospectively evaluated 298...
3.
Zara F, Specchio N, Striano P, Robbiano A, Gennaro E, Paravidino R, et al.
Epilepsia
. 2013 Jan;
54(3):425-36.
PMID: 23360469
Purpose: To dissect the genetics of benign familial epilepsies of the first year of life and to assess the extent of the genetic overlap between benign familial neonatal seizures (BFNS),...
4.
Gaggero R, Consales A, Fazzini F, Mancardi M, Baglietto M, Nozza P, et al.
Epilepsy Res
. 2009 Sep;
87(2-3):184-9.
PMID: 19783404
Objective: To investigate the clinical features and outcome of epilepsy in children under 3 years of age with supratentorial brain tumors. Methods: Patients under 3 years with primary supratentorial hemispheric...
5.
Pintaudi M, Baglietto M, Gaggero R, Parodi E, Pessagno A, Marchi M, et al.
Epilepsy Behav
. 2007 Dec;
12(2):326-31.
PMID: 18063413
Clinical features and electroencephalographic findings of two patients affected by a previously unreported cyclin-dependent kinase-like 5 (CDKL5) gene mutation are described. Both patients had the Hanefeld variant phenotype with early-onset...
6.
Mancardi M, Caruso U, Schiaffino M, Baglietto M, Rossi A, Battaglia F, et al.
Epilepsia
. 2007 Jun;
48(6):1211-3.
PMID: 17553121
Disorders of creatine synthesis or its transporter resulting in neurological impairment with mental retardation and epilepsy have only been recognized in recent years. To date, the epileptic disorder observed in...
7.
Striano P, Mancardi M, Biancheri R, Madia F, Gennaro E, Paravidino R, et al.
Epilepsia
. 2007 Mar;
48(6):1092-6.
PMID: 17381446
Introduction: To determine the occurrence of neuroradiological abnormalities and to perform genotype-phenotype correlations in severe myoclonic epilepsy of infancy (SMEI, Dravet syndrome). Patients And Methods: Alpha-subunit type A of voltage-gated...
8.
Striano P, Specchio N, Biancheri R, Cannelli N, Simonati A, Cassandrini D, et al.
Epilepsy Behav
. 2006 Nov;
10(1):187-91.
PMID: 17129765
Neuronal ceroid lipofuscinoses (NCLs) are characterized by epilepsy, visual failure, psychomotor deterioration, and accumulation of autofluorescent lipopigment. CLN8 mutations result in Northern epilepsy and Turkish variant late infantile NCL. We...
9.
Mancardi M, Striano P, Gennaro E, Madia F, Paravidino R, Scapolan S, et al.
Epilepsia
. 2006 Oct;
47(10):1629-35.
PMID: 17054684
Purpose: The role of the familial background in severe myoclonic epilepsy of infancy (SMEI) has been traditionally emphasized in literature, with 25-70% of the patients having a family history of...
10.
Gaggero R, Haupt R, Paola Fondelli M, De Vescovi R, Marino A, Lanino E, et al.
J Child Neurol
. 2006 Sep;
21(10):861-6.
PMID: 17005102
The long-term evolution to intractable epilepsy in children treated with cyclosporine administered for graft-versus-host-disease after hematopoietic stem cell transplantation was evaluated. In a group of 185 children treated with cyclosporine...