statistiche ricercatore

Continente	#
NA - Nord America	699
EU - Europa	396
AS - Asia	352
SA - Sud America	59
AF - Africa	12
Continente sconosciuto - Info sul continente non disponibili	2
OC - Oceania	1
Totale	1.521

Nazione	#
US - Stati Uniti d'America	684
SG - Singapore	133
RU - Federazione Russa	132
CN - Cina	87
IT - Italia	83
BR - Brasile	40
FI - Finlandia	40
VN - Vietnam	39
HK - Hong Kong	35
IE - Irlanda	28
DE - Germania	26
PL - Polonia	21
GB - Regno Unito	20
FR - Francia	16
SE - Svezia	12
IN - India	11
JP - Giappone	11
KR - Corea	8
AR - Argentina	6
BD - Bangladesh	6
CA - Canada	6
RO - Romania	6
CO - Colombia	5
MX - Messico	5
ZA - Sudafrica	5
BE - Belgio	4
CL - Cile	4
TN - Tunisia	4
AT - Austria	3
MY - Malesia	3
PK - Pakistan	3
UA - Ucraina	3
EC - Ecuador	2
IQ - Iraq	2
KG - Kirghizistan	2
KZ - Kazakistan	2
UY - Uruguay	2
UZ - Uzbekistan	2
AU - Australia	1
BH - Bahrain	1
CR - Costa Rica	1
DZ - Algeria	1
EU - Europa	1
HN - Honduras	1
HR - Croazia	1
IL - Israele	1
IR - Iran	1
JO - Giordania	1
KE - Kenya	1
LB - Libano	1
MA - Marocco	1
NI - Nicaragua	1
NL - Olanda	1
NP - Nepal	1
PA - Panama	1
PH - Filippine	1
TR - Turchia	1
XK - ???statistics.table.value.countryCode.XK???	1
Totale	1.521

Nome	#
DIAGNOSIS AND FOLLOW-UP OF COMPLEX CONGENITAL MALFORMATIONS/MENTAL RETARDATION (MRA/MR)	237
Intellectual disabilitiy in developmental age	213
12q14.3 microdeletion involving HMGA2 gene cause a Silver-Russell syndrome-like phenotype: A case report and review of the literature	194
INTELLECTUAL DISABILITY, EPILEPSY AND MILD DYSMORPHISMS DUE 22q11.2 DISTAL DUPLICATION: CLINICAL AND MOLECULAR CHARACTERIZATION OF A 0.5 Mb MINIMAL CRITICAL REGION	191
Array CGH identifies a 823 kb Microduplication at 22q 11.22 encompassing the Rab36 gene in a Child with Autism Spectrum Disorder and Mild Dysmorphism	175
Unusual paroxysmal autonomic manifestations in a 22 month old girl	123
CUTANEOUS MANIFESTATIONS IN PEDIATRIC COELIAC DISEASE	121
Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability	108
The “Honeymoon Phase” in Children with Type 1 Diabetes Mellitus (T1DM): Frequency, Duration and Predictive Factors at Onset.	107
Cutis verticis gyrata and Noonan syndrome: report of two cases with pathogenetic variant in SOS1 gene	104
Totale	1.573

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	105	7	19	1	4	1	4	3	7	11	25	4	19
2022/2023	165	16	34	8	22	10	25	7	15	15	1	8	4
2023/2024	70	5	11	2	4	3	12	8	3	0	1	5	16
2024/2025	181	4	15	21	16	12	2	15	8	9	20	19	40
2025/2026	706	64	11	30	63	67	133	112	72	48	57	24	25
2026/2027	4	4	0	0	0	0	0	0	0	0	0	0	0
Totale													1.573

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