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454 results

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Page 1
Diagnostic imaging in 13 cases of Rasmussen's encephalitis: can early MRI suggest the diagnosis?
Chiapparini L, Granata T, Farina L, Ciceri E, Erbetta A, Ragona F, Freri E, Fusco L, Gobbi G, Capovilla G, Tassi L, Giordano L, Viri M, Dalla Bernardina B, Spreafico R, Savoiardo M. Chiapparini L, et al. Among authors: gobbi g. Neuroradiology. 2003 Mar;45(3):171-83. doi: 10.1007/s00234-002-0923-7. Epub 2003 Feb 12. Neuroradiology. 2003. PMID: 12684722
Rasmussen's encephalitis: early characteristics allow diagnosis.
Granata T, Gobbi G, Spreafico R, Vigevano F, Capovilla G, Ragona F, Freri E, Chiapparini L, Bernasconi P, Giordano L, Bertani G, Casazza M, Dalla Bernardina B, Fusco L. Granata T, et al. Among authors: gobbi g. Neurology. 2003 Feb 11;60(3):422-5. doi: 10.1212/wnl.60.3.422. Neurology. 2003. PMID: 12578922 Clinical Trial.
Experience with immunomodulatory treatments in Rasmussen's encephalitis.
Granata T, Fusco L, Gobbi G, Freri E, Ragona F, Broggi G, Mantegazza R, Giordano L, Villani F, Capovilla G, Vigevano F, Bernardina BD, Spreafico R, Antozzi C. Granata T, et al. Among authors: gobbi g. Neurology. 2003 Dec 23;61(12):1807-10. doi: 10.1212/01.wnl.0000099074.04539.e0. Neurology. 2003. PMID: 14694056
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations.
Striano P, Mancardi MM, Biancheri R, Madia F, Gennaro E, Paravidino R, Beccaria F, Capovilla G, Dalla Bernardina B, Darra F, Elia M, Giordano L, Gobbi G, Granata T, Ragona F, Guerrini R, Marini C, Mei D, Longaretti F, Romeo A, Siri L, Specchio N, Vigevano F, Striano S, Tortora F, Rossi A, Minetti C, Dravet C, Gaggero R, Zara F. Striano P, et al. Among authors: gobbi g. Epilepsia. 2007 Jun;48(6):1092-6. doi: 10.1111/j.1528-1167.2007.01020.x. Epub 2007 Mar 22. Epilepsia. 2007. PMID: 17381446 Free article.
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations.
Canafoglia L, Gennaro E, Capovilla G, Gobbi G, Boni A, Beccaria F, Viri M, Michelucci R, Agazzi P, Assereto S, Coviello DA, Di Stefano M, Rossi Sebastiano D, Franceschetti S, Zara F. Canafoglia L, et al. Among authors: gobbi g. Epilepsia. 2012 Dec;53(12):2120-7. doi: 10.1111/j.1528-1167.2012.03718.x. Epilepsia. 2012. PMID: 23205931 Free article.
White matter and cerebellar involvement in alternating hemiplegia of childhood.
Severino M, Pisciotta L, Tortora D, Toselli B, Stagnaro M, Cordani R, Morana G, Zicca A, Kotzeva S, Zanaboni C, Montobbio G, Rossi A, De Grandis E; IBAHC Consortium. Severino M, et al. J Neurol. 2020 May;267(5):1300-1311. doi: 10.1007/s00415-020-09698-3. Epub 2020 Jan 16. J Neurol. 2020. PMID: 31950366
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution.
Agostinelli S, Traverso M, Accorsi P, Beccaria F, Belcastro V, Capovilla G, Cappanera S, Coppola A, Dalla Bernardina B, Darra F, Ferretti M, Elia M, Galeone D, Giordano L, Gobbi G, Nicita F, Parisi P, Pezzella M, Spalice A, Striano S, Tozzi E, Vignoli A, Minetti C, Zara F, Striano P, Verrotti A. Agostinelli S, et al. Among authors: gobbi g. Eur J Neurol. 2013 May;20(5):856-9. doi: 10.1111/j.1468-1331.2012.03871.x. Epub 2012 Sep 30. Eur J Neurol. 2013. PMID: 23020086 Free article.
Clinical dissection of early onset absence epilepsy in children and prognostic implications.
Agostinelli S, Accorsi P, Beccaria F, Belcastro V, Canevini MP, Capovilla G, Cappanera S, Dalla Bernardina B, Darra F, Del Gaudio L, Elia M, Falsaperla R, Giordano L, Gobbi G, Minetti C, Nicita F, Parisi P, Pavone P, Pezzella M, Sesta M, Spalice A, Striano S, Tozzi E, Traverso M, Vari S, Vignoli A, Zamponi N, Zara F, Striano P, Verrotti A; SINP (Società Italiana Neurologia Pediatrica) Collaborative Working Group. Agostinelli S, et al. Among authors: gobbi g. Epilepsia. 2013 Oct;54(10):1761-70. doi: 10.1111/epi.12341. Epub 2013 Aug 27. Epilepsia. 2013. PMID: 24032425 Free article.
454 results