IRIS
DI MATTEO, GIGLIOLA
 Distribuzione geografica
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Continente #
NA - Nord America 14.121
EU - Europa 1.939
AS - Asia 1.667
SA - Sud America 305
AF - Africa 22
Continente sconosciuto - Info sul continente non disponibili 1
Totale 18.055
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Nazione #
US - Stati Uniti d'America 14.074
SG - Singapore 799
IT - Italia 443
DE - Germania 411
CN - Cina 378
BR - Brasile 251
IE - Irlanda 193
HK - Hong Kong 180
UA - Ucraina 167
FR - Francia 140
RU - Federazione Russa 138
GB - Regno Unito 124
SE - Svezia 74
VN - Vietnam 74
FI - Finlandia 58
KR - Corea 48
IN - India 47
NL - Olanda 46
PL - Polonia 38
BE - Belgio 34
ES - Italia 27
CA - Canada 26
AR - Argentina 22
ID - Indonesia 19
KG - Kirghizistan 19
IR - Iran 17
JP - Giappone 16
AT - Austria 15
BD - Bangladesh 15
MX - Messico 15
TR - Turchia 12
ZA - Sudafrica 10
CO - Colombia 8
PK - Pakistan 8
CZ - Repubblica Ceca 7
EC - Ecuador 7
CL - Cile 6
UZ - Uzbekistan 6
CH - Svizzera 5
IQ - Iraq 5
PT - Portogallo 5
PE - Perù 4
TN - Tunisia 4
AE - Emirati Arabi Uniti 3
BG - Bulgaria 3
EG - Egitto 3
JO - Giordania 3
LT - Lituania 3
MY - Malesia 3
PH - Filippine 3
SA - Arabia Saudita 3
VE - Venezuela 3
DO - Repubblica Dominicana 2
IL - Israele 2
NG - Nigeria 2
PY - Paraguay 2
RO - Romania 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AM - Armenia 1
BY - Bielorussia 1
BZ - Belize 1
GA - Gabon 1
GD - Grenada 1
GR - Grecia 1
GT - Guatemala 1
GY - Guiana 1
HU - Ungheria 1
KE - Kenya 1
LB - Libano 1
MN - Mongolia 1
NO - Norvegia 1
OM - Oman 1
PA - Panama 1
PS - Palestinian Territory 1
QA - Qatar 1
RS - Serbia 1
SC - Seychelles 1
TL - Timor Orientale 1
UY - Uruguay 1
Totale 18.055
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Città #
Wilmington 3.750
Woodbridge 3.570
Houston 2.992
Singapore 476
Fairfield 426
Chandler 366
Ann Arbor 351
Ashburn 332
Beijing 196
Seattle 193
Hong Kong 179
Dublin 163
Rome 143
Jacksonville 139
Cambridge 132
Medford 122
Dearborn 102
Santa Clara 89
The Dalles 82
New York 77
Los Angeles 75
Munich 60
Lawrence 55
San Diego 36
Buffalo 35
Menlo Park 33
Milan 33
Chicago 32
Brussels 30
São Paulo 30
Dallas 28
Council Bluffs 27
Ho Chi Minh City 25
London 21
Warsaw 20
Nuremberg 19
Moscow 18
Zhengzhou 18
Hefei 16
Nanjing 16
Phoenix 16
Salt Lake City 16
Brooklyn 15
Chennai 15
Mülheim 15
Engelhard 14
Pune 14
Redondo Beach 14
San Mateo 14
Helsinki 13
Jakarta 13
Poplar 13
Frankfurt am Main 12
Atlanta 11
Hanoi 11
Montreal 11
Redwood City 11
Seoul 11
Tokyo 11
Barcelona 10
Stockholm 10
Bologna 9
Denver 9
Norwalk 9
Shanghai 9
St. George 9
Verona 9
Amsterdam 8
Boardman 8
Catania 8
Center 8
Orem 8
Toronto 8
Turku 8
University Park 8
Ardabil 7
Brno 7
Florence 7
Johannesburg 7
Kraków 7
North Bergen 7
Rio de Janeiro 7
San Francisco 7
Creede 6
Hangzhou 6
Palo Alto 6
Dong Ket 5
Guangzhou 5
Kunming 5
Lappeenranta 5
Mountain View 5
Mumbai 5
Nanchang 5
Palermo 5
Porto Alegre 5
Radomsko 5
Sterling 5
Wroclaw 5
Ankara 4
Boston 4
Totale 15.037
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Nome #
Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency 486
Chronic Granulomatous Disease Presenting with Salmonella Brain Abscesses. 468
Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy 461
Pancytopenia and severe sepsis in an adult case of congenital X-linked agammaglobulinemia (XLA) 460
Early-onset monocyte-B-natural killer-dendritic cells' deficiency successfully treated with hematopoietic stem cell transplantation. 459
Dual-regulated lentiviral vector for gene therapy of X-linked chronic granulomatosis 454
Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: An Italian multicenter study 450
Novel X-linked inhibitor of apoptosis mutation in very early-onset inflammatory bowel disease child successfully treated with HLA-haploidentical hemapoietic stem cells transplant after removal of αβ+T and B cells 444
Visceral leishmaniasis revealing chronic granulomatous diseases in a child 443
The impact of TACI mutations: from hypogammaglobulinemia in infancy to autoimmunity in adulthood 441
A variable degree of autoimmunity in the pedigree of a patient with type 1 diabetes homozygous for the PTPN22 1858T variant 437
A Familiar CD4 Lymphopenia? 437
. Early-onset monocyte-B-natural killer-dendritic cells’ deficiency successfully treated with hematopoietic stem cell transaplantation 434
CD4 linfocitopenia di padre in figlio: cammino obbligato verso una ipogammaglobulinemia? 426
Immune deficiency caused by impaired expression of nuclear factor-kappaB essential modifier (NEMO) because of a mutation in the 5' untranslated region of the NEMO gene. 419
Combined immunodeficiency due to JAK3 mutation in a child presenting with skin granuloma 407
The impact of TACI mutations in children affected with hypogammaglobulinemia and in their relatives with autoimmunity: a matter of age. 406
L’evoluzione clinica di un paziente con diagnosi iniziale di ipogammaglobulinemia transitoria dell’Infanzia (THI) da un difetto selettivo di IgA (sIgAD) all’immunodeficienza Comune Variabile(CVID). 405
Defective B-cell proliferation and maintenance of long-term memory in patients with chronic granulomatous disease 403
Successful treatment with percutaneous transhepatic alcoholization of a liver abscess in a child with chronic granulomatous disease 402
Serratia marcescens Osteomyelitis in a Newborn with Chronic Granulomatous 395
Dysplasia of Granulocytes in a Patient with HPV Disease, Recurrent Infections, and B Lymphopenia: A Novel Variant of WHIM Syndrome? 392
Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience 383
Caratterizzazione clinica di pazienti con ipogammaglobulinemia. 366
Clinical characterization of hypogammaglobulinemia. 360
Identification of a Btk mutation in a dysgammaglobulinemic patient with reduced B cells: XLA diagnosis or not? 358
Molecular characterization of TNFRSF13B gene in pediatric patients with hypogammaglobulinemia. 356
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 355
Insight into B-cell development and differentiation 352
Functional analysis of peripheral blood B cells in a case of atypical XLA 347
Late-onset combined immune-deficiency due to LIGIV mutations in a 12 years old patient 331
Dual response to human papilloma virus vaccine in an immunodeficiency disorder: Resolution of plantar warts and persistence of condylomas 306
Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies. Front Immunol. 2019 Apr 11;10:316. doi: 10.3389/fimmu.2019.00316. eCollection 2019. Erratum in: Front Immunol. 2019 May 31;10:1184. 298
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 294
The dilemma of PID diagnosis. The identification of a BTK mutation is not sufficient to TAG a disease. 272
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 263
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children 228
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 219
First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia 209
The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment 204
Diagnostic Approach to Monogenic Inflammatory Bowel Disease in Clinical Practice: A Ten-Year Multicentric Experience 195
Impaired X-CGD T cell compartment is gp91phox-NADPH oxidase independent 192
Urogenital Abnormalities in Adenosine Deaminase Deficiency 184
Corrigendum : Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies (Frontiers in Immunology (2019) 10 (316) DOI: 10.3389/fimmu.2019.00316) 179
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 176
Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child with Intermittent Neutropenia 175
Novel Compound Heterozygous Mutations in IL-7 Receptor α Gene in a 15-Month-Old Girl Presenting With Thrombocytopenia, Normal T Cell Count and Maternal Engraftment. 173
Clinical, immunological, and functional characterization of six patients with very high IgM levels 171
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection 161
Molecular characterization and novel mutations in a large cohort of patients with chronic granulomatous disease 148
Partial T cell defects and expanded CD56bright NK cells in an SCID patient carrying hypomorphic mutation in the IL2RG gene 113
Clinical, Immunological, and Molecular Variability of RAG Deficiency: A Retrospective Analysis of 22 RAG Patients 109
Altered NK-cell compartment and dysfunctional NKG2D/NKG2D-ligand axis in patients with ataxia-telangiectasia 102
The Evolutionary Scenario of Pediatric Unclassified Primary Antibody Deficiency to Adulthood 91
Case Report: EBV Chronic Infection and Lymphoproliferation in Four APDS Patients: The Challenge of Proper Characterization, Therapy, and Follow-Up 89
Immunological aspects of x-linked chronic granulomatous disease female carriers 81
Case Report: Altered NK Cell Compartment and Reduced CXCR4 Chemotactic Response of B Lymphocytes in an Immunodeficient Patient With HPV-Related Disease 76
Case Report: Crossing a rugged road in a primary immune regulatory disorder 75
IPINeT Ped-unPAD Study: Goals, Design, and Preliminary Results 73
Gastric cancer, inflammatory bowel disease and polyautoimmunity in a 17-year-old boy: CTLA-4 deficiency successfully treated with Abatacept 71
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease 64
Characterization of AR-CGD female patient with a novel homozygous deletion in CYBC1 gene presenting with unusual clinical phenotype 63
Humoral and cellular response following vaccination with the BNT162b2 mRNA COVID-19 vaccine in patients affected by primary immunodeficiencies 63
Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature 63
Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait? 61
Case report: Neonatal-onset inflammatory bowel disease due to novel compound heterozygous mutations in DUOX2 55
Cryptococcal Meningitis and Post-Infectious Inflammatory Response Syndrome in a Patient With X-Linked Hyper IgM Syndrome: A Case Report and Review of the Literature 51
Corrigendum: Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult Patient 49
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for the diagnosis of inborn errors of immunity (IEI) 49
Natural history of type 1 diabetes on an immunodysregulatory background with genetic alteration in B-cell activating factor receptor: A case report 42
TNFRSF13B genetic characterization of pediatric patients with hypogammaglobulinemia. 42
Corrigendum to: Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency 36
Totale 18.302
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Categoria #
all - tutte 48.443
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 48.443
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.373 0 0 0 0 0 309 382 347 128 82 95 30
2021/2022690 27 74 27 35 86 57 22 38 74 39 43 168
2022/2023917 91 91 44 107 58 212 103 73 67 4 49 18
2023/2024402 45 39 14 22 46 99 13 20 27 7 1 69
2024/20251.813 58 376 182 117 72 137 163 96 165 164 200 83
2025/20261.474 265 150 292 360 337 70 0 0 0 0 0 0
Totale 18.302