statistiche ricercatore

Continente	#
NA - Nord America	866
EU - Europa	818
AS - Asia	680
SA - Sud America	68
AF - Africa	18
OC - Oceania	3
Continente sconosciuto - Info sul continente non disponibili	2
Totale	2.455

Nazione	#
US - Stati Uniti d'America	833
GB - Regno Unito	264
CN - Cina	236
SG - Singapore	229
DE - Germania	158
SE - Svezia	105
IT - Italia	99
HK - Hong Kong	76
BR - Brasile	55
IN - India	40
RU - Federazione Russa	39
CA - Canada	30
NL - Olanda	30
IE - Irlanda	21
FR - Francia	20
FI - Finlandia	19
KR - Corea	18
ID - Indonesia	17
TR - Turchia	17
BE - Belgio	14
JP - Giappone	13
PL - Polonia	11
CI - Costa d'Avorio	10
UA - Ucraina	10
VN - Vietnam	10
DK - Danimarca	6
ES - Italia	6
EU - Europa	6
CH - Svizzera	4
BD - Bangladesh	3
IQ - Iraq	3
KZ - Kazakistan	3
SA - Arabia Saudita	3
TW - Taiwan	3
UZ - Uzbekistan	3
ZA - Sudafrica	3
AR - Argentina	2
AT - Austria	2
AU - Australia	2
CL - Cile	2
CO - Colombia	2
MA - Marocco	2
MX - Messico	2
NO - Norvegia	2
PY - Paraguay	2
TN - Tunisia	2
UY - Uruguay	2
VE - Venezuela	2
A2 - ???statistics.table.value.countryCode.A2???	1
BG - Bulgaria	1
EC - Ecuador	1
EE - Estonia	1
HR - Croazia	1
HU - Ungheria	1
IL - Israele	1
JM - Giamaica	1
KE - Kenya	1
KH - Cambogia	1
KW - Kuwait	1
LU - Lussemburgo	1
MT - Malta	1
NP - Nepal	1
NZ - Nuova Zelanda	1
PH - Filippine	1
PK - Pakistan	1
PT - Portogallo	1
SK - Slovacchia (Repubblica Slovacca)	1
Totale	2.460

Nome	#
A case report with the peculiar concomitance of 2 different genetic syndromes	280
ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases	264
Limb girdle muscular dystrophy due to LAMA2 gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis	254
IgD multiple myeloma paraproteinemia as a cause of myositis	228
Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia	206
Incontinence in late onset pompe disease : an underdiagnosed although potentially treatable condition	197
Longitudinal follow-up and muscle MRI pattern of two siblings with polyglucosan body myopathy due to glycogenin-1 mutation	177
The primary structure of UK114 tumor antigen	175
Steroid-responsive Hashimoto encephalopathy mimicking Creutzfeldt-Jakob disease	164
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families	159
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy	158
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients	147
Spontaneous hydro(syringo)myelic cavity in two unrelated patients with late onset pompe disease: is this a fortuitous association?	138
Sex differences in ischemic stroke during COVID-19 first outbreak in northern Italy	43
Totale	2.590

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	100	0	0	0	0	0	0	10	23	16	9	25	17
2021/2022	191	24	15	7	9	10	8	6	8	31	18	19	36
2022/2023	288	43	38	32	31	25	52	3	21	29	0	10	4
2023/2024	164	6	9	7	6	31	4	16	17	8	14	15	31
2024/2025	471	34	24	17	43	48	18	11	44	30	51	54	97
2025/2026	514	119	82	81	74	82	52	24	0	0	0	0	0
Totale													2.590

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