statistiche ricercatore

Continente	#
NA - Nord America	1.835
EU - Europa	1.361
AS - Asia	490
SA - Sud America	64
Continente sconosciuto - Info sul continente non disponibili	41
AF - Africa	22
OC - Oceania	2
Totale	3.815

Nazione	#
US - Stati Uniti d'America	1.811
GB - Regno Unito	356
RU - Federazione Russa	240
IT - Italia	213
CN - Cina	183
IE - Irlanda	149
SG - Singapore	149
DE - Germania	99
UA - Ucraina	75
SE - Svezia	72
FR - Francia	63
BR - Brasile	51
FI - Finlandia	41
VN - Vietnam	41
HK - Hong Kong	32
KR - Corea	20
CA - Canada	18
ZA - Sudafrica	17
BE - Belgio	13
TR - Turchia	13
ES - Italia	12
IN - India	10
JP - Giappone	9
PL - Polonia	8
BD - Bangladesh	6
IQ - Iraq	6
NL - Olanda	6
PK - Pakistan	5
CZ - Repubblica Ceca	4
ID - Indonesia	4
MX - Messico	4
AR - Argentina	3
AT - Austria	3
SA - Arabia Saudita	3
AU - Australia	2
CL - Cile	2
CO - Colombia	2
EC - Ecuador	2
EG - Egitto	2
IL - Israele	2
VE - Venezuela	2
AE - Emirati Arabi Uniti	1
AL - Albania	1
AM - Armenia	1
BO - Bolivia	1
BY - Bielorussia	1
EU - Europa	1
HN - Honduras	1
JO - Giordania	1
KZ - Kazakistan	1
LT - Lituania	1
LV - Lettonia	1
MA - Marocco	1
MT - Malta	1
MY - Malesia	1
NG - Nigeria	1
NO - Norvegia	1
PH - Filippine	1
PR - Porto Rico	1
PS - Palestinian Territory	1
PY - Paraguay	1
RO - Romania	1
SN - Senegal	1
XK - ???statistics.table.value.countryCode.XK???	1
Totale	3.776

Nome	#
Tarlov cysts: clinical evaluation of an italian cohort of patients.	402
A new thymidine phosphorylase mutation causing elongation of the protein underlies mitochondrial neurogastrointestinal encephalomyopathy	375
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients	351
Cerebellum and neuropsychiatric disorders: insights from ARSACS	330
Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrum	329
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene.	272
Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsies.	268
The first Italian patient with oculopharyngodistal myopathy: Case report and considerations on differential diagnosis.	258
Clinical and biochemical improvement following HSCT in a patient with MNGIE: 1-year follow-up.	256
Hand muscles corticomotor excitability in hereditary spastic paraparesis type 4.	234
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome	212
Neurophthalmologic and Orthoptic Ambulatory Assessments Reveal Ocular and Visual Changes in Patients With Early Alzheimer and Parkinson's Disease	196
null	182
Vitamin D levels in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)	150
Totale	3.815

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	158	0	0	6	9	19	6	18	6	13	19	21	41
2022/2023	263	20	16	41	28	23	52	8	22	25	16	7	5
2023/2024	259	4	2	27	18	7	71	90	7	5	10	2	16
2024/2025	389	5	19	41	21	51	28	11	26	22	20	41	104
2025/2026	1.019	73	128	128	141	230	35	85	36	30	42	15	76
2026/2027	147	41	31	75	0	0	0	0	0	0	0	0	0
Totale													3.815