IRIS
GIARDINO, GIULIANA
 Distribuzione geografica
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Continente #
AS - Asia 4.426
NA - Nord America 3.825
EU - Europa 2.865
SA - Sud America 546
AF - Africa 111
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 4
Totale 11.785
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Nazione #
US - Stati Uniti d'America 3.679
SG - Singapore 1.839
RU - Federazione Russa 1.456
VN - Vietnam 935
CN - Cina 873
IT - Italia 455
BR - Brasile 419
HK - Hong Kong 310
DE - Germania 201
FR - Francia 171
FI - Finlandia 108
GB - Regno Unito 88
CA - Canada 86
IE - Irlanda 84
BD - Bangladesh 80
NL - Olanda 78
IN - India 76
JP - Giappone 69
UA - Ucraina 60
AR - Argentina 50
MX - Messico 42
SE - Svezia 40
KR - Corea 36
TR - Turchia 31
ZA - Sudafrica 31
CI - Costa d'Avorio 26
IQ - Iraq 26
AT - Austria 25
ID - Indonesia 23
CO - Colombia 21
EC - Ecuador 21
PH - Filippine 21
ES - Italia 20
EG - Egitto 19
PL - Polonia 18
TH - Thailandia 15
BE - Belgio 11
MA - Marocco 10
PK - Pakistan 9
AE - Emirati Arabi Uniti 8
AU - Australia 8
AZ - Azerbaigian 8
LT - Lituania 8
UZ - Uzbekistan 8
CL - Cile 7
KZ - Kazakistan 7
SA - Arabia Saudita 7
VE - Venezuela 7
JO - Giordania 6
KE - Kenya 6
MY - Malesia 6
PE - Perù 6
TW - Taiwan 6
CH - Svizzera 5
IL - Israele 5
PY - Paraguay 5
TN - Tunisia 5
JM - Giamaica 4
MT - Malta 4
TT - Trinidad e Tobago 4
UY - Uruguay 4
BO - Bolivia 3
CZ - Repubblica Ceca 3
DK - Danimarca 3
GR - Grecia 3
HU - Ungheria 3
LB - Libano 3
OM - Oman 3
PS - Palestinian Territory 3
SI - Slovenia 3
SK - Slovacchia (Repubblica Slovacca) 3
AD - Andorra 2
BA - Bosnia-Erzegovina 2
CR - Costa Rica 2
CY - Cipro 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
ET - Etiopia 2
EU - Europa 2
GY - Guiana 2
KG - Kirghizistan 2
LV - Lettonia 2
MM - Myanmar 2
NP - Nepal 2
PT - Portogallo 2
RO - Romania 2
AL - Albania 1
AM - Armenia 1
BB - Barbados 1
BF - Burkina Faso 1
BG - Bulgaria 1
BW - Botswana 1
BY - Bielorussia 1
CV - Capo Verde 1
CW - ???statistics.table.value.countryCode.CW??? 1
GF - Guiana Francese 1
GM - Gambi 1
GT - Guatemala 1
HN - Honduras 1
HR - Croazia 1
Totale 11.770
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Città #
Singapore 885
San Jose 568
Chandler 441
Moscow 334
Beijing 299
Hong Kong 280
Ashburn 278
Santa Clara 247
Ho Chi Minh City 238
Hanoi 177
Hefei 144
The Dalles 113
Los Angeles 96
Millbury 91
Lauterbourg 83
Dong Ket 76
Tokyo 64
Naples 60
New York 58
Nanjing 56
Amsterdam 53
Princeton 52
Buffalo 50
Boston 48
Munich 47
Jacksonville 45
Des Moines 43
Wilmington 42
Napoli 41
Redondo Beach 40
Da Nang 39
Dallas 39
São Paulo 36
Frankfurt am Main 35
Haiphong 35
Council Bluffs 30
Helsinki 29
Seattle 29
Brooklyn 28
Houston 28
Lawrence 26
London 26
Orem 26
Turku 26
Milan 24
Seoul 24
Chicago 23
Falkenstein 20
Montreal 20
Rio de Janeiro 20
Toronto 20
Woodbridge 20
Nuremberg 19
Ottawa 19
Pune 19
Atlanta 18
Biên Hòa 18
Rome 17
Düsseldorf 16
Mexico City 16
Nanchang 15
Phoenix 15
Poplar 15
Boardman 14
Thái Bình 14
Warsaw 14
Chennai 13
Thái Nguyên 13
Cairo 12
Tianjin 12
Falls Church 11
Johannesburg 11
Bologna 10
Dublin 10
Hebei 10
Hải Dương 10
Manchester 10
Quito 10
Stockholm 10
Vienna 10
Belo Horizonte 9
Dhaka 9
Kochi 9
Quận Bình Thạnh 9
Brasília 8
Brussels 8
Bắc Giang 8
Denver 8
Medellín 8
Querétaro 8
Vũng Tàu 8
Wuhan 8
Ankara 7
Baghdad 7
Baku 7
Bangkok 7
Bogotá 7
Mumbai 7
Neenah 7
Roubaix 7
Totale 6.189
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Nome #
DiGeorge-like syndrome in a child with a 3p12.3 deletion involving miRNA-4273 born to a diabetic mother 243
Case report: EBV-related eye orbits and sinuses lymphohistiocytic infiltration responsive to rituximab in a patient with X lymphoproliferative syndrome type 1 198
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 184
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. 184
Clinical, Immunological, and Functional Characterization of Six Patients with Very High IgM Levels 176
Intrathecal amphotericin B therapy in a patient with X-linked chronic granulomatous disease and refractory cerebral invasive aspergillosis 168
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet) 165
Immunodeficienze primitive: cosa c’è di nuovo 165
TLR9 signaling in patients with ectodermal dysplasia and immunodeficiency associated with Nuclear Factor Essential Modulator (NEMO) mutations 164
DiGeorge-like Syndrome in a Child with a 3p12.3 Deletion Involving MIR4273 Gene Born to a Mother with Gestational Diabetes Mellitus 163
CD4+ T Cell Defects in a Mulibrey Patient With Specific TRIM37 Mutations 160
Gastrointestinal involvement in patients affected with 22q11.2 deletion syndrome 159
The Inborn Errors of Immunity—Virtual Consultation System Platform in Service for the Italian Primary Immunodeficiency Network: Results from the Validation Phase 154
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 154
Steroid treatment in Ataxia-Telangiectasia induces alterations of functional magnetic resonance imaging during prono-supination task. 154
Severe combined immunodeficiency-an update 153
Novel STAT1 gain of function mutation and suppurative infections 153
Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network 151
Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis 151
Phenotypic characterization and outcome of paediatric patients affected with haemophagocytic syndrome of unknown genetic cause. 147
Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network 147
From murine to human Nude/SCID: the thymus, T-cell development and the missing link. 144
Elevated IgM levels in a patient with a de novo 13Q12.3Q14.11 deletion, mimicking an A-T like phenotype 142
Diagnostics of Primary immunodeficiencies through next-generation sequencing 142
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors 140
FOXN1: a master regulator gene of thymic epithelial development program 140
Rare solid tumors in a patient with Wiskott–Aldrich syndrome after hematopoietic stem cell transplantation: case report and review of literature 139
Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency 137
DiGeorge Syndrome 137
Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy: insights into genotype-phenotype correlation 136
Immunophenotype anomalies predict the development of autoimmune cytopenia in 22q11.2 Deletion Syndrome 136
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype 135
Clinical outcome, incidence, and SARS-CoV-2 infection-fatality rates in Italian patients with inborn errors of immunity 134
Unraveling the link between ectodermal disorders and primary immunodeficiencies 133
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for diagnosing inborn errors of immunity 132
Unbalanced Immune System: Immunodeficiencies and Autoimmunity 132
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 132
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 131
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects 129
Altered signaling through IL-12 receptor in children with very high serum IgE levels 128
Interleukin 12 receptor deficiency in a child with recurrent bronchopneumonia and very high IgE levels 126
Severe combined immunodeficiences: new and old scenarios 125
Efficacy of very-low-dose betamethasone on neurological symptoms in ataxia-telangiectasia 124
3-dimensional poly(3-caprolactone) scaffold containing skin-derived fibroblasts and keratinocytes supports in vitro HSCs differentiation in T-lineage-committed cells 124
Intergenerational familial phenotipic variability in 22Q11.2 subjects: a multicenter study within the italian primary immunodeficiencies network (IPINET) 124
FOXN1 in cell development and human diseases 123
Complement system network in cell physiology and in human diseases 121
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 120
SCID-like phenotype associated with an inhibitory autoreactive immunoglobulin 119
Retrospective analysis of 21 pediatric patients affected with hemophagocytic syndrome of unknown genetic cause: clinical features and outcome 119
Three Unrelated Patients of Roma Ethnicity from a Single Center Carrying the Same Deletion in MYD88 Gene: A Founder Effect? 118
Altered regulatory mechanisms governing cell survival in children affected with clustering of autoimmune disorders 118
Targeted next-generation sequencing revealed MYD88 deficiency in a child with chronic yersiniosis and granulomatous lymphadenitis 118
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 118
Clinical Phenotype, Immunological Abnormalities, and Genomic Findings in Patients with DiGeorge Spectrum Phenotype without 22q11.2 Deletion 118
Hyper IgM syndrome presenting as chronic suppurative lung disease 117
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 117
FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches 117
Respiratory Manifestations in Primary Immunodeficiencies: Findings From a Pediatric and Adult Cohort 116
Epigenetic Alterations in Inborn Errors of Immunity 116
NADPH Oxidase Deficiency: A Multisystem Approach 114
Chronic granulomatous disease with gastrointestinal presentation: diagnostic pitfalls and novel ultrastructural findings 113
SARS-CoV-2 Infection in the Immunodeficient Host: Necessary and Dispensable Immune Pathways 113
Characterization of a WAS splice-site variant in a patient with Wiskott-Aldrich syndrome 112
Genetic basis of altered central tolerance and autoimmune diseases: a lesson from AIRE mutations 111
A Bronchovascular Anomaly in a Patient With 22q11.2 Deletion Syndrome 111
The R156H variation in IL-12Rβ1 is not a mutation 110
Mechanisms of immune tolerance breakdown in inborn errors of immunity 109
Betamethasone therapy in Ataxia-Telangiectasia: unraveling the rationale of this serendipitous observation on the basis of the pathogenesis 108
A case of Incontinentia Pigmenti associated with congenital absence of portal vein system and nodular regenerative hyperplasia 104
Clinical Manifestations of 22q11.2 Deletion Syndrome 104
T-Cell Immunodeficiencies With Congenital Alterations of Thymic Development: Genes Implicated and Differential Immunological and Clinical Features 103
MicroRNA dysregulation in ataxia telangiectasia 96
Case Report: Severe Rhabdomyolysis and Multiorgan Failure After ChAdOx1 nCoV-19 Vaccination 96
COVID-19 Vaccination in Patients with Inborn Errors of Immunity Reduces Hospitalization and Critical Care Needs Related to COVID-19: a USIDNET Report 93
Non Invasive Assessment of Lung Disease in Ataxia Telangiectasia by High-Field Magnetic Resonance Imaging 93
Insight into IKBKG/NEMO locus: report of new mutations and complex genomic rearrangements leading to incontinentia pigmenti disease 92
Immunological Aspects of Kabuki Syndrome: A Retrospective Multicenter Study of the Italian Primary Immunodeficiency Network (IPINet) 92
Two Brothers with Atypical UNC13D-Related Hemophagocytic Lymphohistiocytosis Characterized by Massive Lung and Brain Involvement 88
Intergenerational anticipation of disease onset in people with multiple autoimmune syndrome. 87
B cells from nuclear factor kB essential modulator deficient patients fail to differentiate to antibody secreting cells in response to TLR9 ligand 86
Clinical and immunological features in a cohort of patients with partial DiGeorge syndrome followed at a single center 86
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations 86
Report of the Italian Cohort with Activated Phosphoinositide 3-Kinase δ Syndrome in the Target Therapy Era 85
Alterations of the autoimmune regulator transcription factor and failure of central tolerance: APECED as a model 84
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency 82
The Evolutionary Scenario of Pediatric Unclassified Primary Antibody Deficiency to Adulthood 81
Immune tolerance breakdown in inborn errors of immunity: Paving the way to novel therapeutic approaches 81
Activated phosphoinositide 3-dinase delta syndrome (APDS): An update 73
Ataxia teleangiectasia: molecular biology, diagnosis and treatment. 70
Asthma: An Undermined State of Immunodeficiency 70
Risk factors predisposing to the development of hypogammaglobulinemia and infections post-Rituximab 63
Antibody Deficiency in Patients with Biallelic KARS1 Mutations 62
Oral thrush and onychomycosis 61
Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity 60
Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia 58
Does NADPH Oxidase Deficiency Cause Artery Dilatation in Humans? 58
Immunological basis of virus-host interaction in COVID-19 57
Metabolite and thymocyte development defects in ADA-SCID mice receiving enzyme replacement therapy 52
Recurrent cold suppurative granulomatous lymphadenitis 49
Totale 11.923
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Categoria #
all - tutte 36.428
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 36.428
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20266.039 599 460 631 548 1.087 224 705 291 789 371 166 168
2026/202735 35 0 0 0 0 0 0 0 0 0 0 0
Totale 11.991