statistiche ricercatore

Nome	#
Mild Lafora disease: Clinical, neurophysiologic, and genetic findings	118
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture	96
Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlations	88
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations	83
Genetic diagnosis in Lafora disease: Genotype-phenotype correlations and diagnostic pitfalls	72
Effects in neocortical neurons of mutations of the Nav1.2 Na+ channel causing benign familial neonatal-infantile seizures	67
Short and long interval cortical inhibition in patients with Unverricht-Lundborg and Lafora body disease	58
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals	57
Expanding sialidosis spectrum by genome-wide screening: NEU1 mutations in adult-onset myoclonus	56
Progressive Myoclonus Epilepsies Diagnostic Yield with Next-Generation Sequencing in Previously Unsolved Cases	51
Totale	746

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	58	0	0	0	0	31	0	0	12	3	12	0	0
2021/2022	83	18	0	0	1	11	7	0	16	1	13	6	10
2022/2023	94	12	0	1	10	16	15	0	7	17	3	13	0
2023/2024	85	0	6	8	12	3	22	6	5	2	5	3	13
2024/2025	254	16	12	3	25	14	22	34	49	9	17	38	15
2025/2026	122	63	11	31	15	2	0	0	0	0	0	0	0
Totale													746