statistiche ricercatore

Nazione	#
US - Stati Uniti d'America	529
DE - Germania	128
SG - Singapore	122
BR - Brasile	100
CN - Cina	95
IT - Italia	94
IE - Irlanda	85
SE - Svezia	71
FI - Finlandia	63
HK - Hong Kong	34
PL - Polonia	34
IN - India	15
FR - Francia	11
VN - Vietnam	11
CA - Canada	10
GB - Regno Unito	9
RU - Federazione Russa	7
AR - Argentina	6
MX - Messico	5
BE - Belgio	4
CZ - Repubblica Ceca	4
EC - Ecuador	4
ID - Indonesia	4
MA - Marocco	4
AT - Austria	3
AZ - Azerbaigian	3
CO - Colombia	3
IQ - Iraq	3
BD - Bangladesh	2
CI - Costa d'Avorio	2
LT - Lituania	2
UZ - Uzbekistan	2
VE - Venezuela	2
ZA - Sudafrica	2
AE - Emirati Arabi Uniti	1
BA - Bosnia-Erzegovina	1
CY - Cipro	1
DO - Repubblica Dominicana	1
EG - Egitto	1
FJ - Figi	1
HN - Honduras	1
HR - Croazia	1
KG - Kirghizistan	1
KR - Corea	1
KZ - Kazakistan	1
LA - Repubblica Popolare Democratica del Laos	1
ME - Montenegro	1
NL - Olanda	1
NP - Nepal	1
PA - Panama	1
PE - Perù	1
PH - Filippine	1
PT - Portogallo	1
PY - Paraguay	1
SA - Arabia Saudita	1
SN - Senegal	1
TR - Turchia	1
UA - Ucraina	1
UY - Uruguay	1
Totale	1.498

Nome	#
De novo mutation in SLC25A22 gene: expansion of the clinical and electroencephalographic phenotype	232
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment	157
A novel SLC1A4 homozygous mutation causing congenital microcephaly, epileptic encephalopathy and spastic tetraparesis: a video-EEG and tractography – case study	155
8q22.1 Microduplication Syndrome: Why the Brain Should Be Spared? A Literature Review and a Case Report	153
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease	124
Aripiprazole-induced Tardive Dyskinesia in 13 Years Old Girl Successfully Treated with Biperiden: A Case Report.	120
Electroclinical history of a five-year-old girl with GRIN1-related early-onset epileptic encephalopathy: a video-case study	108
Il Parent Training in età evolutiva	106
A de novo truncating mutation in ASXL1 associated with segmental overgrowth	96
Alstrom's Syndrome: Neurological Manifestations and Genetics	71
Bardet-Biedl Syndrome: A Brief Overview on Clinics and Genetics	58
Gender affects early psychomotor milestones and long-term neurodevelopment of preterm infants	47
null	46
CNTN2 gene: probabile causa di Encefalopatia Epilettica fenotipo Lennox-Gastaut like.	45
null	24
Totale	1.542

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	50	0	0	0	0	0	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	78	4	15	6	6	2	25	0	3	0	9	1	7
2024/2025	510	7	4	13	25	16	58	65	84	104	38	41	55
2025/2026	429	74	57	137	62	86	13	0	0	0	0	0	0
Totale													1.542