statistiche ricercatore

Continente	#
EU - Europa	874
Totale	874

Nazione	#
IT - Italia	874
Totale	874

Nome	#
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy	132
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy	119
Copy number variations and susceptibility to lateral temporal epilepsy: A study of 21 pedigrees	106
Progressive myoclonic epilepsies Definitive and still undetermined causes	103
In response: DEPDC5 mutations in epilepsy with auditory features	91
Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy	89
Mild Lafora disease: Clinical, neurophysiologic, and genetic findings	76
Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlations	55
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations	50
Cannabidiol in Pharmacoresistant Epilepsy: Clinical Pharmacokinetic Data From an Expanded Access Program	31
Ocular phenotype and electroretinogram abnormalities in Lafora disease and correlation with disease stage	27
Progressive Myoclonus Epilepsies Diagnostic Yield with Next-Generation Sequencing in Previously Unsolved Cases	23
Totale	902

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	172	0	0	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	66	1	12	6	13	2	9	7	2	2	3	2	7
2024/2025	33	13	14	6	0	0	0	0	0	0	0	0	0
Totale													902