statistiche ricercatore

Continente	#
NA - Nord America	1.696
EU - Europa	1.296
AS - Asia	483
SA - Sud America	60
AF - Africa	22
Continente sconosciuto - Info sul continente non disponibili	2
OC - Oceania	2
Totale	3.561

Nazione	#
US - Stati Uniti d'America	1.673
GB - Regno Unito	356
RU - Federazione Russa	240
CN - Cina	183
IT - Italia	152
IE - Irlanda	149
SG - Singapore	149
DE - Germania	99
UA - Ucraina	75
SE - Svezia	69
FR - Francia	62
BR - Brasile	49
FI - Finlandia	41
VN - Vietnam	40
HK - Hong Kong	31
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
IQ - Iraq	6
NL - Olanda	6
BD - Bangladesh	5
CZ - Repubblica Ceca	4
MX - Messico	4
PK - Pakistan	4
AR - Argentina	3
AT - Austria	3
SA - Arabia Saudita	3
AU - Australia	2
CL - Cile	2
EG - Egitto	2
ID - Indonesia	2
IL - Israele	2
VE - Venezuela	2
AE - Emirati Arabi Uniti	1
AL - Albania	1
AM - Armenia	1
BO - Bolivia	1
BY - Bielorussia	1
CO - Colombia	1
EC - Ecuador	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
PS - Palestinian Territory	1
PY - Paraguay	1
RO - Romania	1
SN - Senegal	1
XK - ???statistics.table.value.countryCode.XK???	1
Totale	3.561

Nome	#
A new thymidine phosphorylase mutation causing elongation of the protein underlies mitochondrial neurogastrointestinal encephalomyopathy	364
Tarlov cysts: clinical evaluation of an italian cohort of patients.	347
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients	342
Cerebellum and neuropsychiatric disorders: insights from ARSACS	314
Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrum	307
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene.	257
Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsies.	256
Clinical and biochemical improvement following HSCT in a patient with MNGIE: 1-year follow-up.	245
The first Italian patient with oculopharyngodistal myopathy: Case report and considerations on differential diagnosis.	244
Hand muscles corticomotor excitability in hereditary spastic paraparesis type 4.	217
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome	203
Neurophthalmologic and Orthoptic Ambulatory Assessments Reveal Ocular and Visual Changes in Patients With Early Alzheimer and Parkinson's Disease	185
null	182
Vitamin D levels in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)	137
Totale	3.600

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	24	0	0	0	0	0	0	0	0	0	0	0	24
2021/2022	208	17	33	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	951	73	128	128	141	230	35	85	36	30	42	15	8
Totale													3.600