TAGLIA, ILARIA
 Distribuzione geografica
Continente #
NA - Nord America 818
EU - Europa 318
AS - Asia 76
OC - Oceania 9
AF - Africa 3
SA - Sud America 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 1.228
Nazione #
US - Stati Uniti d'America 817
RU - Federazione Russa 127
IT - Italia 73
IE - Irlanda 47
SE - Svezia 44
SG - Singapore 41
CN - Cina 14
FI - Finlandia 13
HK - Hong Kong 12
AU - Australia 9
IN - India 7
CI - Costa d'Avorio 3
FR - Francia 3
GB - Regno Unito 3
UA - Ucraina 3
BR - Brasile 2
AR - Argentina 1
CA - Canada 1
DE - Germania 1
EE - Estonia 1
EU - Europa 1
JO - Giordania 1
NL - Olanda 1
PH - Filippine 1
PT - Portogallo 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 1.228
Città #
Santa Clara 348
Fairfield 75
Dublin 47
Ashburn 40
Woodbridge 39
Cambridge 38
Singapore 38
Seattle 35
Chandler 34
Houston 30
Wilmington 18
Princeton 14
Altamura 12
Boston 12
Lawrence 12
Ann Arbor 9
Melbourne 9
Siena 8
Florence 7
Beijing 6
Mumbai 6
Shanghai 5
Jacksonville 4
San Diego 4
Abidjan 3
Cisano Bergamasco 3
Laurel 3
Medford 3
Milan 3
Palermo 3
Sesto Fiorentino 3
Bari 2
Cagliari 2
Catanzaro 2
Hong Kong 2
New York 2
Norwalk 2
Perugia 2
Rio Grande 2
San Giovanni Rotondo 2
Andover 1
Bratislava 1
Chennevières-sur-marne 1
Favara 1
Federal 1
Guangzhou 1
Helsinki 1
Hillsboro 1
Islington 1
Kent 1
Lisbon 1
Livorno 1
Lonigo 1
Manila 1
Menlo Park 1
Paris 1
Piediluco 1
Rome 1
Rui'an 1
San Mateo 1
Stockholm 1
Tallinn 1
Toronto 1
Yubileyny 1
Totale 913
Nome #
Neurogenetica clinica 128
Three new mutations in CSF1R gene in 3 italian patients with hereditary diffuse leukoencephalopathy with axonal spheroids 117
Primary familial brain calcification: Genetic analysis and clinical spectrum 116
A Novel CSF1R Mutation in a Patient with Clinical and Neuroradiological Features of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids 116
Two novel HTRA1 mutations in a European CARASIL patient 114
Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R gene 111
Sporadic PEO caused by a novel POLG variation and a Twinkle mutation: digenic inheritance? 111
Two new heterozygous mutations of HTRA1 gene in a caucasian patient affected by CARASIL 100
Hereditary cerebral small vessel diseases: A review 97
Mutation screening of HTRA1 gene in NOTCH3-negative patients with cerebral small vessel disease 81
Mitochondrial abnormalities in neck extensor myopathy: histological and molecular studies of six patients 73
Progressive external ophtalmoplegia in a patient with both a twinkle mutation and a novel polg1 variation: a case of digenic inheritance? 66
Totale 1.230
Categoria #
all - tutte 3.302
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 3.302


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202071 0 0 0 0 0 0 18 18 16 8 9 2
2020/202149 9 4 2 5 3 0 3 3 7 3 5 5
2021/202262 3 4 3 6 1 2 1 5 4 3 2 28
2022/2023205 24 36 19 3 5 48 24 23 4 2 16 1
2023/202457 4 11 19 2 5 5 3 2 0 0 1 5
2024/2025582 16 47 41 74 223 181 0 0 0 0 0 0
Totale 1.230