statistiche ricercatore

Continente	#
NA - Nord America	1.356
EU - Europa	499
AS - Asia	374
SA - Sud America	49
AF - Africa	9
Continente sconosciuto - Info sul continente non disponibili	1
Totale	2.288

Nazione	#
US - Stati Uniti d'America	1.342
IT - Italia	157
SG - Singapore	140
GB - Regno Unito	123
CN - Cina	88
SE - Svezia	56
HK - Hong Kong	53
DE - Germania	41
BR - Brasile	37
VN - Vietnam	31
RU - Federazione Russa	26
TR - Turchia	22
FI - Finlandia	20
FR - Francia	15
UA - Ucraina	13
ID - Indonesia	12
BG - Bulgaria	8
CZ - Repubblica Ceca	8
AR - Argentina	6
BE - Belgio	6
JP - Giappone	6
NL - Olanda	6
CA - Canada	5
IN - India	5
KR - Corea	5
ES - Italia	4
LT - Lituania	4
MA - Marocco	4
MX - Messico	4
PL - Polonia	4
AT - Austria	3
IR - Iran	3
MY - Malesia	3
ZA - Sudafrica	3
CO - Colombia	2
IE - Irlanda	2
KG - Kirghizistan	2
PE - Perù	2
AZ - Azerbaigian	1
BZ - Belize	1
CH - Svizzera	1
CR - Costa Rica	1
EU - Europa	1
GD - Grenada	1
IQ - Iraq	1
JM - Giamaica	1
KE - Kenya	1
LA - Repubblica Popolare Democratica del Laos	1
NO - Norvegia	1
PA - Panama	1
PK - Pakistan	1
SD - Sudan	1
SK - Slovacchia (Repubblica Slovacca)	1
UY - Uruguay	1
VE - Venezuela	1
Totale	2.288

Nome	#
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes	430
A 5-year clinical follow-up study from the Italian National Registry for FSHD	357
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry	327
Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy.	274
The Italian FSHD registry: An enhanced data integration and analytics framework for smart health care	257
Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis	239
D4Z4 reduced allele in myopathic subjects with no FSHD phenotype: why inconsistency between molecular and clinical data should prompt us to further investigations.	231
Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy	191
Totale	2.306

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	251	0	0	0	0	0	0	68	59	24	44	41	15
2021/2022	236	11	16	46	7	8	10	12	20	28	13	48	17
2022/2023	242	26	30	21	16	39	19	6	23	25	1	19	17
2023/2024	158	2	10	6	14	19	11	11	17	6	11	8	43
2024/2025	381	15	14	3	30	69	57	24	45	47	14	21	42
2025/2026	379	43	18	41	83	132	57	5	0	0	0	0	0
Totale													2.306