IRIS
FILLA, ALESSANDRO
 Distribuzione geografica
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Continente #
EU - Europa 1.075
NA - Nord America 561
AS - Asia 390
OC - Oceania 43
AF - Africa 25
SA - Sud America 18
Continente sconosciuto - Info sul continente non disponibili 3
Totale 2.115
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Nazione #
US - Stati Uniti d'America 487
DE - Germania 412
IT - Italia 186
GB - Regno Unito 154
IN - India 96
CN - Cina 83
CA - Canada 69
NL - Olanda 40
RU - Federazione Russa 38
UA - Ucraina 36
AU - Australia 35
VN - Vietnam 32
CZ - Repubblica Ceca 28
FR - Francia 27
ES - Italia 26
JP - Giappone 25
KR - Corea 22
RO - Romania 21
TR - Turchia 20
ID - Indonesia 19
PL - Polonia 16
PT - Portogallo 15
SA - Arabia Saudita 14
BR - Brasile 11
IL - Israele 11
AT - Austria 10
IE - Irlanda 10
PH - Filippine 10
GR - Grecia 9
DK - Danimarca 8
NZ - Nuova Zelanda 8
TH - Thailandia 8
PK - Pakistan 7
BE - Belgio 6
JO - Giordania 6
ZA - Sudafrica 6
AE - Emirati Arabi Uniti 5
DZ - Algeria 5
HK - Hong Kong 5
SE - Svezia 5
TW - Taiwan 5
CI - Costa d'Avorio 4
FI - Finlandia 4
IR - Iran 4
LT - Lituania 4
SG - Singapore 4
HU - Ungheria 3
MA - Marocco 3
MK - Macedonia 3
MY - Malesia 3
AR - Argentina 2
BH - Bahrain 2
CH - Svizzera 2
CO - Colombia 2
CY - Cipro 2
EE - Estonia 2
EU - Europa 2
LK - Sri Lanka 2
LV - Lettonia 2
MX - Messico 2
RS - Serbia 2
TZ - Tanzania 2
A1 - Anonimo 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BG - Bulgaria 1
BO - Bolivia 1
CM - Camerun 1
CU - Cuba 1
EG - Egitto 1
IM - Isola di Man 1
IQ - Iraq 1
KE - Kenya 1
LR - Liberia 1
MO - Macao, regione amministrativa speciale della Cina 1
MT - Malta 1
NP - Nepal 1
PA - Panama 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
SY - Repubblica araba siriana 1
UY - Uruguay 1
VE - Venezuela 1
YE - Yemen 1
Totale 2.115
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Città #
Ashburn 118
Nürnberg 36
Dong Ket 31
Beijing 30
Wuhan 22
Mumbai 18
Houston 17
Ottawa 15
Leawood 13
Tübingen 13
Amsterdam 12
London 12
Milan 11
Naples 11
Tokyo 11
Napoli 9
New York 9
Ann Arbor 8
Bedlington 8
Bangalore 7
Jackson 7
Jakarta 7
Moscow 7
Mountain View 7
Rome 7
Surrey 7
Toronto 7
Woodbridge 7
Colorado Springs 6
Dresden 6
Frignano 6
Illmitz 6
Madrid 6
Seattle 6
Shanghai 6
Stockton 6
Wilmington 6
Ankara 5
Athens 5
Blacktown 5
Chennai 5
Guelph 5
Leeds 5
Lisbon 5
New Delhi 5
Phoenix 5
Boardman 4
Bologna 4
Bristol 4
Cambridge 4
Cape Town 4
Chicago 4
Costa Mesa 4
Dearborn 4
Desio 4
Groningen 4
Gurgaon 4
Paris 4
Puerto Real 4
Riyadh 4
Siena 4
Sydney 4
Atlanta 3
Birmingham 3
Boise 3
Bordeaux 3
Chestertown 3
Chongqing 3
Correzzana 3
Cuiabá 3
District Heights 3
Dublin 3
Florence 3
Indianapolis 3
Islamabad 3
Jeddah 3
Kingston Upon Thames 3
Kumar 3
Lancing 3
Manchester 3
Melbourne 3
Milpitas 3
Mineral Point 3
Mississauga 3
Novosibirsk 3
Parsippany 3
Pisa 3
Polska 3
Pontedera 3
Seoul 3
Shenzhen 3
Springfield 3
St Petersburg 3
Suri 3
Taipei 3
The Dalles 3
Torino 3
Verona 3
Warsaw 3
Wool 3
Totale 744
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Nome #
Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6., file e268a72c-d446-4c8f-e053-1705fe0a812c 567
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study, file e268a72c-bbdf-4c8f-e053-1705fe0a812c 261
Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum., file e268a72c-ba0f-4c8f-e053-1705fe0a812c 245
PINK1 homozygous W437X mutation in a patient with apparent dominant transmission of parkinsonism., file e268a72c-bdf0-4c8f-e053-1705fe0a812c 133
Suppression of myoclonus in SCA2 by piracetam., file e268a72c-d3b1-4c8f-e053-1705fe0a812c 115
Benign hereditary chorea: clinical and neuroimaging features in an Italian family., file e268a72c-d070-4c8f-e053-1705fe0a812c 106
Novel mutation of SACS gene in a Spanish family with autosomal recessive spastic ataxia, file e268a72c-beca-4c8f-e053-1705fe0a812c 92
Ataxia with oculomotor apraxia type 1 in southern italy: late onset and variable phenotype., file e268a72c-b54b-4c8f-e053-1705fe0a812c 86
Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum, file e268a72c-b54a-4c8f-e053-1705fe0a812c 83
Epoetin alfa increases frataxin production in Friedreich's ataxia without affecting hematocrit., file e268a72c-c547-4c8f-e053-1705fe0a812c 82
Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion., file e268a72c-c581-4c8f-e053-1705fe0a812c 68
Very late onset in ataxia oculomotor apraxia type I., file e268a72c-bd70-4c8f-e053-1705fe0a812c 63
A randomized clinical trial of lithium in multiple system atrophy., file e268a72c-d46a-4c8f-e053-1705fe0a812c 55
Complex phenotype in an Italian family with a novel mutation in SPG3A., file e268a72c-cfab-4c8f-e053-1705fe0a812c 54
A novel mutation in SACS gene in a family from southern Italy, file e268a72c-bdb0-4c8f-e053-1705fe0a812c 47
Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms., file e268a72c-c582-4c8f-e053-1705fe0a812c 40
Senataxin, defective in ataxia oculomotor apraxia type 2, is involved in the defense against oxidative DNA damage., file e268a72c-ba10-4c8f-e053-1705fe0a812c 25
Growth hormone response to arginine test differentiates between two subgroups of Huntington's disease patients, file e268a731-198d-4c8f-e053-1705fe0a812c 17
A randomized trial of varenicline (Chantix) for the treatment of spinocerebellar ataxia type 3., file e268a72c-d5cf-4c8f-e053-1705fe0a812c 14
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis., file e268a72d-fb74-4c8f-e053-1705fe0a812c 13
A combined nucleic acid and protein analysis in Friedreich ataxia: implications for diagnosis, pathogenesis and clinical trial design., file e268a72d-fd68-4c8f-e053-1705fe0a812c 8
Self-rated health status in spinocerebellar ataxia--results from a European multicenter study., file e268a72c-c36e-4c8f-e053-1705fe0a812c 3
A novel NKX2.1 mutation in a family with hypothyroidism and benign hereditary chorea., file e268a72c-c02b-4c8f-e053-1705fe0a812c 1
Modifications of resting state networks in spinocerebellar ataxia type 2, file e268a72d-0d56-4c8f-e053-1705fe0a812c 1
Episodic ataxia and severe infantile phenotype in spinocerebellar ataxia type 14: expansion of the phenotype and novel mutations, file f3a3aff3-7c86-4656-9587-85ca29f21062 1
Totale 2.180
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Categoria #
all - tutte 3.831
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 3.831
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201983 0 0 0 0 0 0 0 0 0 24 29 30
2019/2020271 23 22 22 19 26 19 32 19 23 26 20 20
2020/2021326 27 25 36 13 36 22 17 21 17 42 33 37
2021/2022243 36 17 28 16 20 13 13 20 17 22 17 24
2022/2023124 9 8 9 6 8 9 6 12 8 15 23 11
2023/2024304 8 9 17 32 33 34 111 19 13 28 0 0
Totale 2.180