IRIS
GALLO, VERA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 744
EU - Europa 312
AS - Asia 267
AF - Africa 15
OC - Oceania 3
Totale 1.341
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 732
IT - Italia 145
CN - Cina 114
SG - Singapore 89
UA - Ucraina 36
VN - Vietnam 36
IE - Irlanda 28
FI - Finlandia 22
SE - Svezia 19
FR - Francia 18
DE - Germania 16
NL - Olanda 13
CA - Canada 12
TR - Turchia 12
CI - Costa d'Avorio 9
GB - Regno Unito 9
IN - India 9
EG - Egitto 6
AU - Australia 3
CH - Svizzera 2
HK - Hong Kong 2
SA - Arabia Saudita 2
SI - Slovenia 2
IL - Israele 1
JP - Giappone 1
MT - Malta 1
PL - Polonia 1
TW - Taiwan 1
Totale 1.341
Salva come PNG Salva come JPEG
Città #
Chandler 198
Singapore 83
Beijing 42
Dong Ket 36
Jacksonville 35
Napoli 34
Nanjing 32
Millbury 29
Princeton 26
Des Moines 25
Santa Clara 25
Wilmington 25
Houston 15
Ashburn 14
Boston 13
Amsterdam 10
Milan 10
Ottawa 9
Pune 8
Falls Church 7
Hebei 7
Neenah 7
Seattle 7
Woodbridge 7
Boardman 6
Naples 5
Rome 5
Xi'an 5
Dallas 4
Mcallen 4
Nanchang 4
Shenyang 4
Brescia 3
Cairo 3
Lawrence 3
Tianjin 3
Ann Arbor 2
Frankfurt Am Main 2
Genova 2
Hanover 2
Hong Kong 2
Indiana 2
Livorno 2
Los Angeles 2
Montréal 2
Redwood City 2
Riyadh 2
San Giorgio a Cremano 2
Sydney 2
Tappahannock 2
Benevento 1
Birzebbuga 1
Brisbane 1
Casapulla 1
Casoria 1
Castellana Grotte 1
Changchun 1
Changsha 1
Cologne 1
Coquitlam 1
Cormeilles-en-Parisis 1
Council Bluffs 1
Duino-Aurisina 1
Edinburgh 1
Fairfield 1
Fisciano 1
Gesualdo 1
Ghedi 1
Grumo Nevano 1
Guiyang 1
Gulf Breeze 1
Harbin 1
Jupiter 1
Kaohsiung 1
Kingwood 1
Lincoln 1
London 1
Marigliano 1
Mazzano Romano 1
Mercato San Severino 1
Monmouth Junction 1
Monterotondo 1
Mountain View 1
Mumbai 1
Nocera Inferiore 1
Nola 1
Norwalk 1
Providence 1
Qingdao 1
Salerno 1
San Giovanni Rotondo 1
San Mateo 1
Seregno 1
Shaoxing 1
Stockholm 1
Teddington 1
Urbino 1
Wuhan 1
Zurich 1
Totale 830
Salva come PNG Salva come JPEG
Nome #
DiGeorge-like syndrome in a child with a 3p12.3 deletion involving miRNA-4273 born to a diabetic mother 110
TLR9 signaling in patients with ectodermal dysplasia and immunodeficiency associated with Nuclear Factor Essential Modulator (NEMO) mutations 74
Intrathecal amphotericin B therapy in a patient with X-linked chronic granulomatous disease and refractory cerebral invasive aspergillosis 72
Chronic mucocutaneous candidiasis, recurrent herpetic infections and suppurative eyelid infections in a patient carrying a novel gain-of-function mutation in the STAT1 DNA-binding domain 67
Gastrointestinal involvement in patients affected with 22q11.2 deletion syndrome 66
DiGeorge-like Syndrome in a Child with a 3p12.3 Deletion Involving MIR4273 Gene Born to a Mother with Gestational Diabetes Mellitus 60
Clinical, Immunological, and Functional Characterization of Six Patients with Very High IgM Levels 59
Unraveling the link between ectodermal disorders and primary immunodeficiencies 55
Otolarylogical features in a cohort of patients affected with 22q11.2 deletion syndrome: a monocentric survey 53
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects 52
Diagnostics of Primary immunodeficiencies through next-generation sequencing 51
Unbalanced Immune System: Immunodeficiencies and Autoimmunity 47
Severe combined immunodeficiency-an update 45
FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches 45
In Ataxia-Telangiectasia, Oral Betamethasone Administration Ameliorates Lymphocytes Functionality through Modulation of the IL-7/IL-7Rα Axis Paralleling the Neurological Behavior: A Comparative Report of Two Cases 45
Phenotypic characterization and outcome of paediatric patients affected with haemophagocytic syndrome of unknown genetic cause. 44
Immunodeficienze primitive: cosa c’è di nuovo 41
DiGeorge Syndrome 41
B cells from nuclear factor kB essential modulator deficient patients fail to differentiate to antibody secreting cells in response to TLR9 ligand 40
FOXN1 in cell development and human diseases 37
A Bronchovascular Anomaly in a Patient With 22q11.2 Deletion Syndrome 37
FOXN1: a master regulator gene of thymic epithelial development program 35
Intergenerational familial phenotipic variability in 22Q11.2 subjects: a multicenter study within the italian primary immunodeficiencies network (IPINET) 35
Targeted next-generation sequencing revealed MYD88 deficiency in a child with chronic yersiniosis and granulomatous lymphadenitis 34
NADPH Oxidase Deficiency: A Multisystem Approach 34
Evaluation of executive functions in subjects affected with 22Q11.2 deletion syndrome: a neuroanatomical hypothesis 33
Biweekly Hizentra® in Primary Immunodeficiency: a Multicenter, Observational Cohort Study (IBIS) 33
Elevated IgM levels in a patient with a de novo 13Q12.3Q14.11 deletion, mimicking an A-T like phenotype 30
Retrospective analysis of 21 pediatric patients affected with hemophagocytic syndrome of unknown genetic cause: clinical features and outcome 20
The Inborn Errors of Immunity—Virtual Consultation System Platform in Service for the Italian Primary Immunodeficiency Network: Results from the Validation Phase 15
Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET) 13
Totale 1.423
Salva come PNG Salva come JPEG
Categoria #
all - tutte 5.440
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 5.440
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202095 0 0 0 0 9 8 0 0 2 28 34 14
2020/2021138 4 7 11 11 24 10 7 2 8 2 15 37
2021/2022210 7 0 0 6 4 14 1 5 31 25 45 72
2022/2023358 36 44 8 46 54 41 1 33 70 11 10 4
2023/2024150 10 31 8 8 16 15 1 17 10 3 23 8
2024/2025151 40 52 17 10 32 0 0 0 0 0 0 0
Totale 1.423