statistiche ricercatore

Continente	#
EU - Europa	489
Totale	489

Nazione	#
IT - Italia	489
Totale	489

Nome	#
CHD2 variants are a risk factor for photosensitivity in epilepsy	77
PDXK mutations cause polyneuropathy responsive to pyridoxal 5′-phosphate supplementation	65
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome	63
No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1	61
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy	57
Benign familial infantile convulsions: Mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity	57
Generalized Epilepsy with Febrile Seizures Plus (GEFS+): Clinical Spectrum in Seven Italian Families Unrelated to SCN1A, SCN1B, and GABRG2 Gene Mutations	47
Dravet syndrome: Early clinical manifestations and cognitive outcome in 37 Italian patients	30
Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and genetic heterogeneity	29
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications	20
Totale	506

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	11	0	0	0	0	0	0	0	0	0	3	4	4
2019/2020	54	2	1	1	2	7	6	11	6	4	8	6	0
2020/2021	125	2	0	3	59	14	5	5	10	7	14	2	4
2021/2022	109	10	2	3	6	6	9	0	25	8	22	2	16
2022/2023	133	8	8	2	13	18	20	14	10	15	5	16	4
2023/2024	70	4	10	0	11	8	22	3	9	2	1	0	0
Totale													506