statistiche ricercatore

Continente	#
EU - Europa	768
NA - Nord America	701
AS - Asia	457
SA - Sud America	46
AF - Africa	5
Continente sconosciuto - Info sul continente non disponibili	2
OC - Oceania	2
Totale	1.981

Nazione	#
US - Stati Uniti d'America	670
GB - Regno Unito	262
CN - Cina	168
DE - Germania	151
SG - Singapore	123
SE - Svezia	104
IT - Italia	85
HK - Hong Kong	60
BR - Brasile	38
IN - India	37
CA - Canada	29
RU - Federazione Russa	27
NL - Olanda	25
IE - Irlanda	21
FI - Finlandia	19
FR - Francia	18
TR - Turchia	16
KR - Corea	15
BE - Belgio	14
ID - Indonesia	14
UA - Ucraina	10
JP - Giappone	8
PL - Polonia	8
DK - Danimarca	6
EU - Europa	6
CH - Svizzera	4
UZ - Uzbekistan	3
AT - Austria	2
AU - Australia	2
ES - Italia	2
IQ - Iraq	2
KZ - Kazakistan	2
MA - Marocco	2
NO - Norvegia	2
SA - Arabia Saudita	2
TW - Taiwan	2
UY - Uruguay	2
VE - Venezuela	2
ZA - Sudafrica	2
A2 - ???statistics.table.value.countryCode.A2???	1
AR - Argentina	1
BD - Bangladesh	1
BG - Bulgaria	1
CL - Cile	1
CO - Colombia	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
LU - Lussemburgo	1
MT - Malta	1
MX - Messico	1
NP - Nepal	1
PH - Filippine	1
PT - Portogallo	1
SK - Slovacchia (Repubblica Slovacca)	1
Totale	1.986

Nome	#
ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases	228
A case report with the peculiar concomitance of 2 different genetic syndromes	226
Limb girdle muscular dystrophy due to LAMA2 gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis	200
IgD multiple myeloma paraproteinemia as a cause of myositis	198
Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia	171
Incontinence in late onset pompe disease : an underdiagnosed although potentially treatable condition	166
The primary structure of UK114 tumor antigen	148
Longitudinal follow-up and muscle MRI pattern of two siblings with polyglucosan body myopathy due to glycogenin-1 mutation	146
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families	133
Steroid-responsive Hashimoto encephalopathy mimicking Creutzfeldt-Jakob disease	133
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients	127
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy	119
Spontaneous hydro(syringo)myelic cavity in two unrelated patients with late onset pompe disease: is this a fortuitous association?	118
Sex differences in ischemic stroke during COVID-19 first outbreak in northern Italy	1
Totale	2.114

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	166	5	6	18	11	16	10	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	38	38	0	0	0	0	0	0	0	0	0	0	0
Totale													2.114

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