statistiche ricercatore

Continente	#
NA - Nord America	1.744
EU - Europa	1.355
AS - Asia	486
SA - Sud America	62
Continente sconosciuto - Info sul continente non disponibili	41
AF - Africa	22
OC - Oceania	2
Totale	3.712

Nazione	#
US - Stati Uniti d'America	1.721
GB - Regno Unito	356
RU - Federazione Russa	240
IT - Italia	208
CN - Cina	183
IE - Irlanda	149
SG - Singapore	149
DE - Germania	99
UA - Ucraina	75
SE - Svezia	72
FR - Francia	62
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
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	3.673

Nome	#
A new thymidine phosphorylase mutation causing elongation of the protein underlies mitochondrial neurogastrointestinal encephalomyopathy	371
Tarlov cysts: clinical evaluation of an italian cohort of patients.	366
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients	346
Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrum	323
Cerebellum and neuropsychiatric disorders: insights from ARSACS	322
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene.	262
Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsies.	260
Clinical and biochemical improvement following HSCT in a patient with MNGIE: 1-year follow-up.	252
The first Italian patient with oculopharyngodistal myopathy: Case report and considerations on differential diagnosis.	252
Hand muscles corticomotor excitability in hereditary spastic paraparesis type 4.	227
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome	210
Neurophthalmologic and Orthoptic Ambulatory Assessments Reveal Ocular and Visual Changes in Patients With Early Alzheimer and Parkinson's Disease	193
null	182
Vitamin D levels in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)	146
Totale	3.712

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	191	0	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	1.019	73	128	128	141	230	35	85	36	30	42	15	76
2026/2027	44	41	3	0	0	0	0	0	0	0	0	0	0
Totale													3.712