Author

Renzo Guerrini

Professore di Neuropsichiatria Infantile, Universit

Biography

Renzo Guerrini is working in Paediatric Neurology Unit and Laboratories, Children's Hospital A. Meyer-University of Florence, Italy. Renzo Guerrini research interests reflect in his wide range of publications in various national and international journals. Renzo Guerrini has authored several articles along with chapters in different books related to studies.
Title
Cited by
Year
Interpretable surface-based detection of focal cortical dysplasias: a Multi-centre Epilepsy Lesion Detection study
H Spitzer, M Ripart, K Whitaker, F D’Arco, K Mankad, AA Chen, ...Brain 145 (11), 3859-3871, 2022202
18
2022
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum
R Guerrini, V Conti, M Mantegazza, S Balestrini, AS Galanopoulou, ...Physiological Reviews 103 (1), 433-513, 2023202
18
2023
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development
C Chung, X Yang, T Bae, KI Vong, S Mittal, C Donkels, H Westley Phillips, ...Nature genetics 55 (2), 209-220, 2023202
10
2023
Epimutations in both the TESK2 and MMACHC promoters in the Epi-cblC inherited disorder of intracellular metabolism of vitamin B12
A Oussalah, Y Siblini, S Hergalant, C Chéry, P Rouyer, C Cavicchi, ...Clinical epigenetics 14 (1), 1-13, 2022202
10
2022
Fenfluramine provides clinically meaningful reduction in frequency of drop seizures in patients with Lennox–Gastaut syndrome: Interim analysis of an open‐label extension study
KG Knupp, IE Scheffer, B Ceulemans, J Sullivan, KC Nickels, L Lagae, ...Epilepsia 64 (1), 139-151, 2023202
7
2023
An examination of the efficacy and safety of fenfluramine in adults, children, and adolescents with Dravet syndrome in a real‐world practice setting: A report from the …
R Guerrini, N Specchio, Á Aledo‐Serrano, M Pringsheim, F Darra, ...Epilepsia Open (4), 58-58, 2022202
7
2022
The clingen brain malformation variant curation expert panel: Rules for somatic variants in AKT3, MTOR, PIK3CA, and PIK3R2
A Lai, A Soucy, CM El Achkar, AJ Barkovich, Y Cao, M DiStefano, ...Genetics in Medicine 24 (11), 2240-2248, 2022202
7
2022
Seizure outcome of temporal lobe epilepsy surgery in adults and children: a systematic review and meta-analysis
C Barba, S Giometto, E Lucenteforte, S Pellacani, G Matta, A Bettiol, ...Neurosurgery 91 (5), 7-83, 2022202
6
2022
Fenfluramine treatment is associated with improvement in everyday executive function in preschool-aged children (< 5 years) with Dravet syndrome
Fenfluramine treatment is associated with improvement in everyday executive function in preschool-aged children (< years) with Dravet syndromeKI Bishop, PK Isquith, GA Gioia, KG Knupp, IE Scheffer, R Nabbout, ...Epilepsy & Behavior 138, 108994, 2023202
5
2023
Dominant ARF3 variants disrupt Golgi integrity and cause a neurodevelopmental disorder recapitulated in zebrafish
G Fasano, V Muto, FC Radio, M Venditti, N Mosaddeghzadeh, S Coppola, ...Nature Communications 13 (1), 6841, 2022202
5
2022
Clinical features, neuropathology, and surgical outcome in patients with refractory epilepsy and brain somatic variants in the SLC35A2 gene
C Barba, I Blumcke, MR Winawer, T Hartlieb, HC Kang, L Grisotto, ...Neurology 100 (5), e528-e52, 2023202
4
2023
The Genetic Landscape of Complex Childhood‐Onset Hyperkinetic Movement Disorders
B Pérez‐Dueñas, K Gorman, A Marcé‐Grau, JD Ortigoza‐Escobar, ...Movement Disorders 7 (11), 2197-2209, 2022202
3
2022
SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance
A Cordovado, M Schaettin, M Jeanne, V Panasenkava, ...Human Molecular Genetics 31 (19), 335-3340, 0
2
2022
Use of cenobamate for the treatment of focal epilepsy: an Italian expert opinion paper
F Villani, V Cianci, C Di Bonaventura, G Di Gennaro, CA Galimberti, ...Expert Review of Neurotherapeutics 22 (-2), 935-940, 2022202
1
2022
Multimodal mapping of regional brain vulnerability to focal cortical dysplasia
HM Lee, SJ Hong, R Gill, B Caldairou, I Wang, J Zhang, F Deleo, ...Brain, awad060, 2023202
1
2023
Phase 2, placebo-controlled clinical study of oral ganaxolone in PCDH19-clustering epilepsy
Phase 2, placebo-controlled clinical study of oral ganaxolone in PCDH9-clustering epilepsyJ Sullivan, B Gunning, M Zafar, R Guerrini, J Gecz, KL Kolc, Y Zhao, ...Epilepsy Research 9, 072, 2023202
1
2023
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice
SE Sheppard, L Bryant, RN Wickramasekara, C Vaccaro, B Robertson, ...Science advances 9 (0), eade463, 2023202
1
2023

Referred From: https://scholar.google.com/citations?user=ZhiXnioAAAAJ&hl=it

Cited by
Citations 49936
h-index 116
i10-index 567
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