statistiche ricercatore

Nome	#
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment	93
8q22.1 Microduplication Syndrome: Why the Brain Should Be Spared? A Literature Review and a Case Report	86
A novel SLC1A4 homozygous mutation causing congenital microcephaly, epileptic encephalopathy and spastic tetraparesis: a video-EEG and tractography – case study	69
Electroclinical history of a five-year-old girl with GRIN1-related early-onset epileptic encephalopathy: a video-case study	69
Il Parent Training in età evolutiva	59
Aripiprazole-induced Tardive Dyskinesia in 13 Years Old Girl Successfully Treated with Biperiden: A Case Report.	51
De novo mutation in SLC25A22 gene: expansion of the clinical and electroencephalographic phenotype	50
A de novo truncating mutation in ASXL1 associated with segmental overgrowth	33
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease	25
null	24
Gender affects early psychomotor milestones and long-term neurodevelopment of preterm infants	19
CNTN2 gene: probabile causa di Encefalopatia Epilettica fenotipo Lennox-Gastaut like.	17
Bardet-Biedl Syndrome: A Brief Overview on Clinics and Genetics	6
Totale	601

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	70	0	0	0	0	2	5	3	3	1	43	9	4
2020/2021	104	5	4	21	13	11	3	6	10	16	7	2	6
2021/2022	84	1	4	1	3	5	4	13	3	3	20	6	21
2022/2023	238	16	33	11	14	16	19	3	17	100	3	2	4
2023/2024	71	4	15	3	5	2	23	0	3	0	9	1	6
2024/2025	5	5	0	0	0	0	0	0	0	0	0	0	0
Totale													601