statistiche ricercatore

Continente	#
AS - Asia	351
NA - Nord America	344
EU - Europa	209
SA - Sud America	69
Continente sconosciuto - Info sul continente non disponibili	11
AF - Africa	5
AN - Antartide	1
Totale	990

Nazione	#
US - Stati Uniti d'America	324
SG - Singapore	145
IT - Italia	91
CN - Cina	70
BR - Brasile	61
HK - Hong Kong	43
BD - Bangladesh	30
DE - Germania	27
VN - Vietnam	27
FI - Finlandia	16
RU - Federazione Russa	15
GB - Regno Unito	14
FR - Francia	12
TR - Turchia	12
UA - Ucraina	10
CA - Canada	9
IN - India	9
MX - Messico	7
PL - Polonia	6
AR - Argentina	3
NL - Olanda	3
PT - Portogallo	3
AT - Austria	2
EC - Ecuador	2
ID - Indonesia	2
JP - Giappone	2
LT - Lituania	2
PY - Paraguay	2
SA - Arabia Saudita	2
SE - Svezia	2
TH - Thailandia	2
ZA - Sudafrica	2
AE - Emirati Arabi Uniti	1
AO - Angola	1
AQ - Antartide	1
AZ - Azerbaigian	1
BB - Barbados	1
CH - Svizzera	1
CO - Colombia	1
CR - Costa Rica	1
CZ - Repubblica Ceca	1
ES - Italia	1
ET - Etiopia	1
GT - Guatemala	1
IE - Irlanda	1
IL - Israele	1
JM - Giamaica	1
JO - Giordania	1
LA - Repubblica Popolare Democratica del Laos	1
LV - Lettonia	1
MY - Malesia	1
PS - Palestinian Territory	1
RO - Romania	1
SN - Senegal	1
Totale	979

Nome	#
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome	149
ACOX1 gain‐of‐function variation in a 10‐years‐old patient responsive to immunomodulating therapy	124
Family History in Parkinson's Disease: A National Cross-Sectional Study	116
Joubert syndrome-derived induced pluripotent stem cells show altered neuronal differentiation in vitro	102
Novel molecular, structural and clinical findings in an Italian cohort of congenital cataract	82
Establishment of three Joubert syndrome-derived induced pluripotent stem cell (iPSC) lines harbouring compound heterozygous mutations in CC2D2A gene	81
Benign Hereditary Chorea as a Manifestation of HPCA Mutation	79
Heterozygous APTX mutation associated with atypical multiple system atrophy-like phenotype: A case report	79
Expanding the spectrum of clinical severity of AICA-ribosiduria: Report of two siblings with mild phenotype caused by a novel pathogenic variant in ATIC gene	71
Prenatal findings in oral-facial-digital syndrome type VI: Report of three cases and literature review	60
Letter to the Editors: Concerning “SSR4-CDG, an ultra-rare X-linked congenital disorder of glycosylation affecting the TRAP complex: Review of 22 affected individuals including the first adult patient” by Johnsen et al	47
Totale	990

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	12	0	8	0	0	0	0	1	0	0	0	1	2
2022/2023	26	1	0	1	2	0	5	8	3	4	0	2	0
2023/2024	54	3	2	1	6	1	5	2	0	8	0	15	11
2024/2025	255	5	10	7	31	19	16	28	17	20	18	32	52
2025/2026	572	50	63	34	71	57	51	72	35	32	54	32	21
2026/2027	33	28	5	0	0	0	0	0	0	0	0	0	0
Totale													990