statistiche ricercatore

Continente	#
NA - Nord America	867
AS - Asia	737
EU - Europa	702
Continente sconosciuto - Info sul continente non disponibili	55
AF - Africa	53
SA - Sud America	45
OC - Oceania	2
Totale	2.461

Nazione	#
US - Stati Uniti d'America	849
IT - Italia	327
SG - Singapore	211
CN - Cina	205
VN - Vietnam	129
GB - Regno Unito	75
DE - Germania	57
HK - Hong Kong	49
SE - Svezia	43
IN - India	39
KR - Corea	35
FR - Francia	28
RU - Federazione Russa	28
NL - Olanda	27
BR - Brasile	25
CH - Svizzera	23
CI - Costa d'Avorio	21
IE - Irlanda	21
BD - Bangladesh	19
FI - Finlandia	14
CA - Canada	12
ZA - Sudafrica	12
JP - Giappone	11
BG - Bulgaria	10
SC - Seychelles	10
TG - Togo	9
AR - Argentina	7
PL - Polonia	7
BE - Belgio	6
TW - Taiwan	6
UA - Ucraina	6
AT - Austria	5
CL - Cile	5
CZ - Repubblica Ceca	5
EE - Estonia	5
ES - Italia	5
ID - Indonesia	5
JO - Giordania	5
EC - Ecuador	4
IR - Iran	3
LT - Lituania	3
MY - Malesia	3
PH - Filippine	3
TR - Turchia	3
AU - Australia	2
CO - Colombia	2
CR - Costa Rica	2
DK - Danimarca	2
HR - Croazia	2
IQ - Iraq	2
PK - Pakistan	2
TH - Thailandia	2
VE - Venezuela	2
AL - Albania	1
AZ - Azerbaigian	1
BB - Barbados	1
CY - Cipro	1
JM - Giamaica	1
LA - Repubblica Popolare Democratica del Laos	1
LB - Libano	1
MX - Messico	1
NG - Nigeria	1
PA - Panama	1
PS - Palestinian Territory	1
RO - Romania	1
SK - Slovacchia (Repubblica Slovacca)	1
Totale	2.406

Nome	#
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy	327
Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy	295
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism	276
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy	252
Liver transplantation in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical long-term follow-up and pathogenic implications	215
ITA-MNGIE: an Italian regional and national survey for mitochondrial neuro-gastro-intestinal encephalomyopathy.	213
Author Correction: Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome (Scientific Reports, (2020), 10, 1, (4785), 10.1038/s41598-020-61735-3)	211
Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys	200
A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function	194
Metformin as an adjuvant drug against pediatric sarcomas: hypoxia limits therapeutic effects of the drug.	172
A novel ALG14 missense variant in an alive child with myopathy, epilepsy, and progressive cerebral atrophy	106
Totale	2.461

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	214	0	5	13	7	12	13	9	21	28	16	49	41
2022/2023	315	34	37	8	42	21	20	9	15	40	6	43	40
2023/2024	143	5	13	5	5	14	39	3	5	21	16	12	5
2024/2025	416	45	42	24	29	41	28	17	19	8	34	41	88
2025/2026	899	87	99	74	89	106	45	81	27	149	64	56	22
2026/2027	42	30	12	0	0	0	0	0	0	0	0	0	0
Totale													2.461

CRIS Current Research Information System