statistiche ricercatore

Nazione	#
US - Stati Uniti d'America	931
CN - Cina	293
SG - Singapore	227
IT - Italia	203
GB - Regno Unito	162
DE - Germania	101
BD - Bangladesh	98
SE - Svezia	87
HK - Hong Kong	68
VN - Vietnam	65
BR - Brasile	58
IN - India	57
RU - Federazione Russa	43
FR - Francia	35
IE - Irlanda	28
DK - Danimarca	27
CA - Canada	26
NL - Olanda	25
FI - Finlandia	23
ID - Indonesia	18
BE - Belgio	14
JP - Giappone	13
KR - Corea	12
UA - Ucraina	8
CI - Costa d'Avorio	7
AR - Argentina	5
AT - Austria	5
MY - Malesia	5
BG - Bulgaria	4
ES - Italia	4
TR - Turchia	4
AU - Australia	3
BJ - Benin	3
CZ - Repubblica Ceca	3
MX - Messico	3
ZA - Sudafrica	3
AL - Albania	2
CH - Svizzera	2
CO - Colombia	2
EC - Ecuador	2
GR - Grecia	2
IQ - Iraq	2
MA - Marocco	2
RO - Romania	2
SA - Arabia Saudita	2
UZ - Uzbekistan	2
BB - Barbados	1
CL - Cile	1
ET - Etiopia	1
GP - Guadalupe	1
JM - Giamaica	1
KE - Kenya	1
LB - Libano	1
ML - Mali	1
NI - Nicaragua	1
NO - Norvegia	1
NP - Nepal	1
OM - Oman	1
PE - Perù	1
PH - Filippine	1
PK - Pakistan	1
PT - Portogallo	1
QA - Qatar	1
SK - Slovacchia (Repubblica Slovacca)	1
TN - Tunisia	1
TW - Taiwan	1
VE - Venezuela	1
Totale	2.712

Nome	#
Autophagy controls neonatal myogenesis by regulating the GH-IGF1 system through a NFE2L2- and DDIT3-mediated mechanism	341
Deficient nitric oxide signalling impairs skeletal muscle growth and performance : involvement of mitochondrial dysregulation	317
The Fine Tuning of Drp1-Dependent Mitochondrial Remodeling and Autophagy Controls Neuronal Differentiation	308
Acid sphingomyelinase controls early phases of skeletal muscle regeneration by shaping the macrophage phenotype	271
ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis	243
The role of clinical and neuroimaging features in the diagnosis of CADASIL	227
Clinical and genetic features of a cohort of patients with MFN2-related neuropathy	206
The emerging role of acid sphingomyelinase in autophagy	205
ZFYVE26/SPASTIZIN : a close link between complicated hereditary spastic paraparesis and autophagy	171
Case Reports: Novel Missense Variants in the Filamin C Actin Binding Domain Cause Variable Phenotypes	149
Aberrant supracallosal longitudinal bundle : MR features, pathogenesis and associated clinical phenotype	137
Cerebroretinal microangiopathy with calcifications and cysts associated with CTC1 and NDP mutations	123
The spectrum of brainstem malformations associated to mutations of the tubulin genes family : MRI and DTI analysis	109
Totale	2.807

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	8	0	0	0	0	0	0	0	0	0	0	0	8
2021/2022	256	18	16	11	9	16	19	26	17	39	32	12	41
2022/2023	320	41	39	29	21	32	50	6	26	47	2	20	7
2023/2024	164	2	15	12	17	43	14	5	8	2	4	14	28
2024/2025	444	22	26	12	38	49	30	21	50	19	51	44	82
2025/2026	1.005	92	57	105	91	84	62	126	40	80	52	162	54
Totale													2.807

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