IRIS
GIARDINO, GIULIANA
 Distribuzione geografica
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Continente #
AS - Asia 3.293
NA - Nord America 2.679
EU - Europa 2.657
SA - Sud America 497
AF - Africa 92
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 3
Totale 9.226
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Nazione #
US - Stati Uniti d'America 2.577
SG - Singapore 1.750
RU - Federazione Russa 1.455
CN - Cina 764
BR - Brasile 396
IT - Italia 395
VN - Vietnam 296
HK - Hong Kong 249
DE - Germania 194
FI - Finlandia 105
IE - Irlanda 81
FR - Francia 80
GB - Regno Unito 75
NL - Olanda 72
IN - India 56
UA - Ucraina 55
CA - Canada 54
SE - Svezia 40
AR - Argentina 39
MX - Messico 38
TR - Turchia 28
ZA - Sudafrica 27
CI - Costa d'Avorio 25
AT - Austria 24
KR - Corea 24
EC - Ecuador 20
ID - Indonesia 19
CO - Colombia 18
IQ - Iraq 18
PL - Polonia 18
BD - Bangladesh 17
ES - Italia 17
EG - Egitto 16
JP - Giappone 15
BE - Belgio 9
LT - Lituania 8
MA - Marocco 7
AE - Emirati Arabi Uniti 6
KE - Kenya 6
KZ - Kazakistan 6
AU - Australia 5
PE - Perù 5
PY - Paraguay 5
SA - Arabia Saudita 5
UZ - Uzbekistan 5
AZ - Azerbaigian 4
IL - Israele 4
PK - Pakistan 4
CH - Svizzera 3
CL - Cile 3
DK - Danimarca 3
GR - Grecia 3
OM - Oman 3
SI - Slovenia 3
SK - Slovacchia (Repubblica Slovacca) 3
TN - Tunisia 3
UY - Uruguay 3
VE - Venezuela 3
AD - Andorra 2
BA - Bosnia-Erzegovina 2
BO - Bolivia 2
CR - Costa Rica 2
CY - Cipro 2
DZ - Algeria 2
EU - Europa 2
GY - Guiana 2
JM - Giamaica 2
LB - Libano 2
LV - Lettonia 2
MT - Malta 2
MY - Malesia 2
NP - Nepal 2
PS - Palestinian Territory 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
AL - Albania 1
AM - Armenia 1
BB - Barbados 1
BY - Bielorussia 1
CV - Capo Verde 1
CW - ???statistics.table.value.countryCode.CW??? 1
CZ - Repubblica Ceca 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GF - Guiana Francese 1
GM - Gambi 1
HR - Croazia 1
HU - Ungheria 1
IR - Iran 1
KG - Kirghizistan 1
LA - Repubblica Popolare Democratica del Laos 1
LC - Santa Lucia 1
MW - Malawi 1
PA - Panama 1
PH - Filippine 1
RO - Romania 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
TJ - Tagikistan 1
TZ - Tanzania 1
Totale 9.225
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Città #
Singapore 819
Chandler 441
Moscow 334
Beijing 279
Hong Kong 242
Santa Clara 235
Ashburn 187
Hefei 144
Millbury 91
Ho Chi Minh City 80
Dong Ket 76
Los Angeles 76
Nanjing 54
Naples 53
Princeton 52
Amsterdam 48
Boston 47
Munich 47
Jacksonville 42
Wilmington 42
Napoli 41
Des Moines 40
Redondo Beach 40
The Dalles 40
Buffalo 38
Hanoi 37
São Paulo 33
New York 32
Frankfurt am Main 31
Dallas 28
Helsinki 28
Seattle 27
Lawrence 26
Turku 26
Houston 25
Brooklyn 23
Seoul 23
London 22
Falkenstein 20
Woodbridge 20
Pune 19
Rio de Janeiro 19
Milan 18
Orem 18
Ottawa 18
Nuremberg 17
Chicago 16
Düsseldorf 16
Mexico City 16
Atlanta 15
Nanchang 15
Boardman 14
Poplar 14
Tokyo 14
Warsaw 14
Montreal 13
Phoenix 13
Da Nang 11
Falls Church 11
Rome 11
Tianjin 11
Hebei 10
Manchester 10
Quito 10
Stockholm 10
Vienna 10
Belo Horizonte 9
Biên Hòa 9
Bologna 9
Cairo 9
Chennai 9
Johannesburg 9
Kochi 9
Denver 8
Haiphong 8
Querétaro 8
Toronto 8
Ankara 7
Bogotá 7
Brasília 7
Dublin 7
Neenah 7
Roubaix 7
Shenyang 7
Thái Bình 7
Afragola 6
Baghdad 6
Brussels 6
Fairfield 6
Jiaxing 6
Lauterbourg 6
Medellín 6
Nairobi 6
Porto Alegre 6
Quận Bình Thạnh 6
Xi'an 6
Castellana Grotte 5
Florence 5
Manaus 5
Norwalk 5
Totale 4.589
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Nome #
DiGeorge-like syndrome in a child with a 3p12.3 deletion involving miRNA-4273 born to a diabetic mother 215
De novo 13q12.3q14.11 deletion involving BRCA2 gene in a patient with developmental delay, elevated IgM levels, transient ataxia and cerebellar hypoplasia, mimicking an A-T like phenotype. 163
Clinical, Immunological, and Functional Characterization of Six Patients with Very High IgM Levels 150
Intrathecal amphotericin B therapy in a patient with X-linked chronic granulomatous disease and refractory cerebral invasive aspergillosis 140
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 138
TLR9 signaling in patients with ectodermal dysplasia and immunodeficiency associated with Nuclear Factor Essential Modulator (NEMO) mutations 138
Steroid treatment in Ataxia-Telangiectasia induces alterations of functional magnetic resonance imaging during prono-supination task. 135
DiGeorge-like Syndrome in a Child with a 3p12.3 Deletion Involving MIR4273 Gene Born to a Mother with Gestational Diabetes Mellitus 134
Gastrointestinal involvement in patients affected with 22q11.2 deletion syndrome 131
CD4+ T Cell Defects in a Mulibrey Patient With Specific TRIM37 Mutations 127
The Inborn Errors of Immunity—Virtual Consultation System Platform in Service for the Italian Primary Immunodeficiency Network: Results from the Validation Phase 123
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet) 123
Novel STAT1 gain of function mutation and suppurative infections 123
Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis 121
Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency 119
Phenotypic characterization and outcome of paediatric patients affected with haemophagocytic syndrome of unknown genetic cause. 117
Severe combined immunodeficiency-an update 115
Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network 113
Case report: EBV-related eye orbits and sinuses lymphohistiocytic infiltration responsive to rituximab in a patient with X lymphoproliferative syndrome type 1 112
Diagnostics of Primary immunodeficiencies through next-generation sequencing 112
Immunophenotype anomalies predict the development of autoimmune cytopenia in 22q11.2 Deletion Syndrome 112
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects 111
Unraveling the link between ectodermal disorders and primary immunodeficiencies 110
Immunodeficienze primitive: cosa c’è di nuovo 109
Unbalanced Immune System: Immunodeficiencies and Autoimmunity 109
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors 108
Severe combined immunodeficiences: new and old scenarios 108
Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy: insights into genotype-phenotype correlation 108
Clinical outcome, incidence, and SARS-CoV-2 infection-fatality rates in Italian patients with inborn errors of immunity 108
Altered signaling through IL-12 receptor in children with very high serum IgE levels 107
FOXN1: a master regulator gene of thymic epithelial development program 106
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 106
Consensus of the Italian Primary Immunodeficiency Network on transition management from pediatric to adult care in patients affected with childhood-onset inborn errors of immunity 106
Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network 106
From murine to human Nude/SCID: the thymus, T-cell development and the missing link. 105
Intergenerational familial phenotipic variability in 22Q11.2 subjects: a multicenter study within the italian primary immunodeficiencies network (IPINET) 105
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype 104
Genetic basis of altered central tolerance and autoimmune diseases: a lesson from AIRE mutations 101
DiGeorge Syndrome 101
Efficacy of very-low-dose betamethasone on neurological symptoms in ataxia-telangiectasia 100
Elevated IgM levels in a patient with a de novo 13Q12.3Q14.11 deletion, mimicking an A-T like phenotype 100
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 100
FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches 100
Complement system network in cell physiology and in human diseases 100
Autosomal-dominant hyper-IgE syndrome is associated with appearance of infections early in life and/or neonatal rash: Evidence from the Italian cohort of 61 patients with elevated IgE 99
Rare solid tumors in a patient with Wiskott–Aldrich syndrome after hematopoietic stem cell transplantation: case report and review of literature 97
3-dimensional poly(3-caprolactone) scaffold containing skin-derived fibroblasts and keratinocytes supports in vitro HSCs differentiation in T-lineage-committed cells 97
FOXN1 in cell development and human diseases 97
A Bronchovascular Anomaly in a Patient With 22q11.2 Deletion Syndrome 96
Clinical Phenotype, Immunological Abnormalities, and Genomic Findings in Patients with DiGeorge Spectrum Phenotype without 22q11.2 Deletion 96
Chronic granulomatous disease with gastrointestinal presentation: diagnostic pitfalls and novel ultrastructural findings 95
Targeted next-generation sequencing revealed MYD88 deficiency in a child with chronic yersiniosis and granulomatous lymphadenitis 95
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 95
SCID-like phenotype associated with an inhibitory autoreactive immunoglobulin 94
Altered regulatory mechanisms governing cell survival in children affected with clustering of autoimmune disorders 94
Interleukin 12 receptor deficiency in a child with recurrent bronchopneumonia and very high IgE levels 94
Retrospective analysis of 21 pediatric patients affected with hemophagocytic syndrome of unknown genetic cause: clinical features and outcome 94
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for diagnosing inborn errors of immunity 93
Epigenetic Alterations in Inborn Errors of Immunity 93
Mechanisms of immune tolerance breakdown in inborn errors of immunity 92
Hyper IgM syndrome presenting as chronic suppurative lung disease 92
Respiratory Manifestations in Primary Immunodeficiencies: Findings From a Pediatric and Adult Cohort 90
Betamethasone therapy in Ataxia-Telangiectasia: unraveling the rationale of this serendipitous observation on the basis of the pathogenesis 89
NADPH Oxidase Deficiency: A Multisystem Approach 89
Clinical Manifestations of 22q11.2 Deletion Syndrome 89
Long term longitudinal follow-up of an AD-HIES cohort: the impact of early diagnosis and enrollment to IPINet centers on the natural history of Job’s syndrome 88
SARS-CoV-2 Infection in the Immunodeficient Host: Necessary and Dispensable Immune Pathways 88
Insight into IKBKG/NEMO locus: report of new mutations and complex genomic rearrangements leading to incontinentia pigmenti disease 86
T-Cell Immunodeficiencies With Congenital Alterations of Thymic Development: Genes Implicated and Differential Immunological and Clinical Features 85
The R156H variation in IL-12Rβ1 is not a mutation 84
MicroRNA dysregulation in ataxia telangiectasia 78
Non Invasive Assessment of Lung Disease in Ataxia Telangiectasia by High-Field Magnetic Resonance Imaging 77
A case of Incontinentia Pigmenti associated with congenital absence of portal vein system and nodular regenerative hyperplasia 77
Three Unrelated Patients of Roma Ethnicity from a Single Center Carrying the Same Deletion in MYD88 Gene: A Founder Effect? 76
B cells from nuclear factor kB essential modulator deficient patients fail to differentiate to antibody secreting cells in response to TLR9 ligand 76
Two Brothers with Atypical UNC13D-Related Hemophagocytic Lymphohistiocytosis Characterized by Massive Lung and Brain Involvement 76
Characterization of a WAS splice-site variant in a patient with Wiskott-Aldrich syndrome 74
Intergenerational anticipation of disease onset in people with multiple autoimmune syndrome. 72
Case Report: Severe Rhabdomyolysis and Multiorgan Failure After ChAdOx1 nCoV-19 Vaccination 72
Alterations of the autoimmune regulator transcription factor and failure of central tolerance: APECED as a model 71
The Evolutionary Scenario of Pediatric Unclassified Primary Antibody Deficiency to Adulthood 68
COVID-19 Vaccination in Patients with Inborn Errors of Immunity Reduces Hospitalization and Critical Care Needs Related to COVID-19: a USIDNET Report 68
Immunological Aspects of Kabuki Syndrome: A Retrospective Multicenter Study of the Italian Primary Immunodeficiency Network (IPINet) 68
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency 66
Clinical and immunological features in a cohort of patients with partial DiGeorge syndrome followed at a single center 64
Activated phosphoinositide 3-dinase delta syndrome (APDS): An update 61
Report of the Italian Cohort with Activated Phosphoinositide 3-Kinase δ Syndrome in the Target Therapy Era 60
Ataxia teleangiectasia: molecular biology, diagnosis and treatment. 58
Immune tolerance breakdown in inborn errors of immunity: Paving the way to novel therapeutic approaches 57
Asthma: An Undermined State of Immunodeficiency 57
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations 53
Oral thrush and onychomycosis 51
Antibody Deficiency in Patients with Biallelic KARS1 Mutations 49
Does NADPH Oxidase Deficiency Cause Artery Dilatation in Humans? 46
Risk factors predisposing to the development of hypogammaglobulinemia and infections post-Rituximab 43
Immunological basis of virus-host interaction in COVID-19 42
Immunodeficiency diagnosis: a Mondrian or Pollock scenario? 39
Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia 37
Metabolite and thymocyte development defects in ADA-SCID mice receiving enzyme replacement therapy 37
Recurrent cold suppurative granulomatous lymphadenitis 35
Totale 9.388
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Categoria #
all - tutte 29.898
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 29.898
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021177 0 0 0 0 0 23 9 20 16 5 26 78
2021/2022522 9 0 1 8 4 16 3 13 103 66 116 183
2022/2023846 91 106 19 98 116 95 8 80 146 45 28 14
2023/2024404 18 70 36 21 26 37 9 42 22 10 81 32
2024/20253.233 124 143 28 26 105 251 300 222 198 334 1.219 283
2025/20263.512 599 460 631 548 1.087 187 0 0 0 0 0 0
Totale 9.429