IRIS
LONGO, ILARIA
 Distribuzione geografica
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Continente #
NA - Nord America 918
EU - Europa 732
AS - Asia 112
OC - Oceania 3
SA - Sud America 2
Totale 1.767
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Nazione #
US - Stati Uniti d'America 915
GB - Regno Unito 228
IE - Irlanda 170
CN - Cina 86
SE - Svezia 74
UA - Ucraina 64
DE - Germania 54
IT - Italia 45
FR - Francia 37
FI - Finlandia 24
BE - Belgio 15
TR - Turchia 10
SG - Singapore 9
RU - Federazione Russa 7
CZ - Repubblica Ceca 4
IN - India 4
AU - Australia 3
CA - Canada 3
ES - Italia 3
IR - Iran 3
NL - Olanda 2
AR - Argentina 1
BR - Brasile 1
EE - Estonia 1
GR - Grecia 1
ME - Montenegro 1
MK - Macedonia 1
RO - Romania 1
Totale 1.767
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Città #
Southend 207
Dublin 169
Fairfield 111
Chandler 98
Ann Arbor 96
Ashburn 72
Woodbridge 65
Jacksonville 54
Houston 52
Cambridge 51
Wilmington 51
Seattle 46
New York 30
Beijing 27
Princeton 23
Nanjing 17
Menlo Park 15
Helsinki 14
Brussels 13
Boardman 12
Shanghai 12
Siena 12
Izmir 10
Dearborn 8
San Diego 8
Milan 7
San Mateo 7
Tianjin 5
Brno 4
Shenyang 4
Singapore 4
Venezia 4
Brindisi 3
Changsha 3
Düsseldorf 3
Hebei 3
Jiaxing 3
Moscow 3
Málaga 3
Nanchang 3
Toronto 3
Trieste 3
Canberra 2
Chiswick 2
Falls Church 2
Kunming 2
Lanzhou 2
London 2
Los Angeles 2
Mestre 2
Nagpur 2
Waanrode 2
Zanjan 2
Acton 1
Augusta 1
Bari 1
Buenos Aires 1
Casoria 1
Caulonia 1
Dallas 1
Falkenstein 1
Florence 1
Gatchina 1
Hangzhou 1
Hendon 1
Hounslow 1
Jinan 1
Lancaster 1
Leawood 1
Melbourne 1
Munich 1
Ningbo 1
Norwalk 1
Palermo 1
Perugia 1
Podgorica 1
Pune 1
Rio Saliceto 1
Sacramento 1
Saint Petersburg 1
San Francisco 1
Skopje 1
Southwark 1
St Petersburg 1
Statte 1
São Paulo 1
Tallinn 1
Trento 1
Washington 1
Totale 1.396
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Nome #
null 182
Genomic differences between retinoma and retinoblastoma 179
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome 165
A 2.6 Mb deletion of 6q24.3-25.1 in a patient with growth failure, cardiac septal defect, thin upperlip and asymmetric dysmorphic ears 163
Private inherited microdeletion/microduplications: implications in clinical practice 160
Autosomal-dominant Alport syndrome: natural history of a disease due to COL4A3 or COL4A4 gene. 151
Advances in Alport syndrome diagnosis using next-generation sequencing 150
Retinoblastoma and mental retardation microdeletion syndrome: clinical characterization and molecular dissection using array CGH 124
Type-IV collagen related diseases 118
Thin glomerular basement membrane disease: clinical significance of a morphological diagnosis a collaborative study of the Italian Renal Immunopathology Group 112
MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness 109
17p13.3 microdeletion including YWHAE and CRK genes: towards a clinical characterization 62
Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array-based detection rate 56
13q Deletion Syndrome Involving RB1: Characterization of a New Minimal Critical Region for Psychomotor Delay 32
Urine-derived podocytes-lineage cells: A promising tool for precision medicine in Alport Syndrome 28
Totale 1.791
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Categoria #
all - tutte 5.521
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 5.521
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020353 51 10 21 53 29 34 31 42 25 26 10 21
2020/2021254 12 30 14 32 9 30 4 34 32 16 29 12
2021/2022201 10 32 9 17 7 6 10 12 8 20 25 45
2022/2023298 17 39 35 40 36 50 12 19 27 10 8 5
2023/2024275 4 9 36 19 5 84 97 3 0 3 1 14
2024/20258 8 0 0 0 0 0 0 0 0 0 0 0
Totale 1.791