statistiche ricercatore

Nome	#
STXBP1 Encephalopathy: A Neurodevelopmental Disorder Including Epilepsy	134
Dramatic effect of levetiracetam in early-onset epileptic encephalopathy due to STXBP1 mutation	122
Efficacy of sodium channel blockers in SCN2A early infantile epileptic encephalopathy	111
Epilepsy Course and Developmental Trajectories in STXBP1-DEE	85
Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies	72
Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations: Functional Studies, Clinical Responses, and Critical Issues for Personalized Therapy	70
Epilepsy features in ARID1B-related Coffin-Siris syndrome	64
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders	62
Sleep-related hypermotor epilepsy (SHE): Contribution of known genes in 103 patients	60
“EPINEO” Monocentric Retrospective Study on Neonatal Seizures: Incidence, ILAE Seizure Type, Epileptic Syndrome, EEG and Etiology	58
Consensus protocol for EEG and amplitude-integrated EEG assessment and monitoring in neonates	32
Case Report: Effect of Targeted Therapy With Carbamazepine in KCNQ2 Neonatal Epilepsy	31
DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders	1
Totale	902

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	88	0	0	0	26	1	3	2	10	6	18	20	2
2021/2022	87	7	2	4	1	3	9	0	20	10	13	4	14
2022/2023	140	13	7	3	10	15	30	0	10	26	1	23	2
2023/2024	94	6	14	7	20	4	12	2	8	5	1	3	12
2024/2025	252	19	13	6	19	21	24	18	33	7	21	36	35
2025/2026	96	56	6	16	18	0	0	0	0	0	0	0	0
Totale													902