statistiche ricercatore

Continente	#
EU - Europa	832
Totale	832

Nazione	#
IT - Italia	832
Totale	832

Nome	#
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy	130
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy	117
Copy number variations and susceptibility to lateral temporal epilepsy: A study of 21 pedigrees	104
Progressive myoclonic epilepsies Definitive and still undetermined causes	100
In response: DEPDC5 mutations in epilepsy with auditory features	89
Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy	86
Mild Lafora disease: Clinical, neurophysiologic, and genetic findings	72
Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlations	50
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations	45
Cannabidiol in Pharmacoresistant Epilepsy: Clinical Pharmacokinetic Data From an Expanded Access Program	25
Ocular phenotype and electroretinogram abnormalities in Lafora disease and correlation with disease stage	21
Progressive Myoclonus Epilepsies Diagnostic Yield with Next-Generation Sequencing in Previously Unsolved Cases	21
Totale	860

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	45	0	0	0	0	0	0	0	0	0	0	24	21
2019/2020	191	9	10	8	13	15	21	31	20	17	27	16	4
2020/2021	129	4	4	3	25	23	1	9	27	1	21	2	9
2021/2022	133	16	0	5	7	11	11	0	27	8	16	12	20
2022/2023	170	21	0	1	15	30	29	0	10	33	7	22	2
2023/2024	57	1	12	6	13	2	9	7	2	2	3	0	0
Totale													860