Renzo Guerrini
Renzo Guerrini
Professore di Neuropsichiatria Infantile, Università di Firenze
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The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc task force of the ILAE Diagnostic Methods Commission 1
I Blümcke, M Thom, E Aronica, DD Armstrong, HV Vinters, A Palmini, ...
Epilepsia 52 (1), 158-174, 2011
Epilepsy in children
J Aicardi
International review of child neurology series, 138-146, 1994
Terminology and classification of the cortical dysplasias
A Palmini, I Najm, G Avanzini, T Babb, R Guerrini, N Foldvary-Schaefer, ...
Neurology 62 (6 suppl 3), S2-S8, 2004
A developmental and genetic classification for malformations of cortical development: update 2012
AJ Barkovich, R Guerrini, RI Kuzniecky, GD Jackson, WB Dobyns
Brain 135 (5), 1348-1369, 2012
A developmental and genetic classification for malformations of cortical development
AJ Barkovich, RI Kuzniecky, GD Jackson, R Guerrini, WB Dobyns
Neurology 65 (12), 1873-1887, 2005
The when and how of Src regulation
JA Cooper, B Howell
Cell 73 (6), 1051-1054, 1993
Classification system for malformations of cortical development: update 2001
AJ Barkovich, RI Kuzniecky, GD Jackson, R Guerrini, WB Dobyns
Neurology 57 (12), 2168-2178, 2001
Lamotrigine and seizure aggravation in severe myoclonic epilepsy
R Guerrini, C Dravet, P Genton, A Belmonte, A Kaminska, O Dulac
Epilepsia 39 (5), 508-512, 1998
Epilepsy in children
R Guerrini
The Lancet 367 (9509), 499-524, 2006
Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology
A Arzimanoglou, J French, WT Blume, JH Cross, JP Ernst, M Feucht, ...
The Lancet Neurology 8 (1), 82-93, 2009
Histopathological findings in brain tissue obtained during epilepsy surgery
I Blumcke, R Spreafico, G Haaker, R Coras, K Kobow, CG Bien, M Pfäfflin, ...
New England Journal of Medicine 377 (17), 1648-1656, 2017
Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex
VL Sheen, VS Ganesh, M Topcu, G Sebire, A Bodell, RS Hill, PE Grant, ...
Nature genetics 36 (1), 69-76, 2004
Proposed criteria for referral and evaluation of children for epilepsy surgery: recommendations of the Subcommission for Pediatric Epilepsy Surgery
JH Cross, P Jayakar, D Nordli, O Delalande, M Duchowny, HG Wieser, ...
Epilepsia 47 (6), 952-959, 2006
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly
K Poirier, N Lebrun, L Broix, G Tian, Y Saillour, C Boscheron, E Parrini, ...
Nature genetics 45 (6), 639-647, 2013
Benign familial neonatal‐infantile seizures: characterization of a new sodium channelopathy
SF Berkovic, SE Heron, L Giordano, C Marini, R Guerrini, RE Kaplan, ...
Annals of neurology 55 (4), 550-557, 2004
Congenital bilateral perisylvian syndrome: study of 31 patients
R Kuzniecky, F Andermann, R Guerrini, TCMC Study
The Lancet 341 (8845), 608-612, 1993
Malformations of cortical development: clinical features and genetic causes
R Guerrini, WB Dobyns
The Lancet Neurology 13 (7), 710-726, 2014
The genetics of Dravet syndrome
C Marini, IE Scheffer, R Nabbout, A Suls, P De Jonghe, F Zara, R Guerrini
Epilepsia 52, 24-29, 2011
Mutations of ARX are associated with striking pleiotropy and consistent genotype–phenotype correlation
M Kato, S Das, K Petras, K Kitamura, K Morohashi, DN Abuelo, M Barr, ...
Human mutation 23 (2), 147-159, 2004
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations
E Parrini, A Ramazzotti, WB Dobyns, D Mei, F Moro, P Veggiotti, C Marini, ...
Brain 129 (7), 1892-1906, 2006
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