statistiche ricercatore

Nome	#
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome	139
PDXK mutations cause polyneuropathy responsive to pyridoxal 5′-phosphate supplementation	124
CHD2 variants are a risk factor for photosensitivity in epilepsy	115
No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1	110
Generalized Epilepsy with Febrile Seizures Plus (GEFS+): Clinical Spectrum in Seven Italian Families Unrelated to SCN1A, SCN1B, and GABRG2 Gene Mutations	103
Benign familial infantile convulsions: Mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity	103
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy	98
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications	88
Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and genetic heterogeneity	71
Dravet syndrome: Early clinical manifestations and cognitive outcome in 37 Italian patients	65
Totale	1.016

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	61	0	0	0	0	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	84	4	10	0	11	8	22	3	9	2	1	4	10
2024/2025	252	4	13	3	18	24	33	25	45	19	18	34	16
2025/2026	244	60	18	107	31	28	0	0	0	0	0	0	0
Totale													1.016