IRIS
DI MATTEO, GIGLIOLA
 Distribuzione geografica
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Continente #
NA - Nord America 15.409
EU - Europa 2.463
AS - Asia 2.146
SA - Sud America 339
Continente sconosciuto - Info sul continente non disponibili 268
AF - Africa 33
OC - Oceania 1
Totale 20.659
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Nazione #
US - Stati Uniti d'America 15.296
SG - Singapore 917
IT - Italia 601
CN - Cina 448
DE - Germania 404
RU - Federazione Russa 298
BR - Brasile 268
FR - Francia 191
HK - Hong Kong 191
IE - Irlanda 190
VN - Vietnam 173
UA - Ucraina 164
GB - Regno Unito 141
SE - Svezia 127
FI - Finlandia 124
BD - Bangladesh 114
CA - Canada 67
JP - Giappone 61
NL - Olanda 57
IN - India 51
KR - Corea 47
PL - Polonia 44
BE - Belgio 37
ES - Italia 30
AR - Argentina 22
KG - Kirghizistan 20
ID - Indonesia 19
IR - Iran 19
MX - Messico 18
TR - Turchia 17
AT - Austria 16
CO - Colombia 16
EC - Ecuador 11
PK - Pakistan 11
ZA - Sudafrica 11
IQ - Iraq 9
CZ - Repubblica Ceca 8
SA - Arabia Saudita 8
UZ - Uzbekistan 8
CL - Cile 7
CH - Svizzera 6
MY - Malesia 6
CR - Costa Rica 5
EG - Egitto 5
PH - Filippine 5
PT - Portogallo 5
JM - Giamaica 4
LT - Lituania 4
NG - Nigeria 4
PA - Panama 4
PE - Perù 4
VE - Venezuela 4
AE - Emirati Arabi Uniti 3
BG - Bulgaria 3
GT - Guatemala 3
JO - Giordania 3
PY - Paraguay 3
SV - El Salvador 3
TN - Tunisia 3
UY - Uruguay 3
AO - Angola 2
AZ - Azerbaigian 2
BY - Bielorussia 2
BZ - Belize 2
DZ - Algeria 2
GR - Grecia 2
HU - Ungheria 2
IL - Israele 2
MA - Marocco 2
NI - Nicaragua 2
PS - Palestinian Territory 2
RO - Romania 2
RS - Serbia 2
TT - Trinidad e Tobago 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AM - Armenia 1
AU - Australia 1
BF - Burkina Faso 1
BH - Bahrain 1
CW - ???statistics.table.value.countryCode.CW??? 1
DO - Repubblica Dominicana 1
GA - Gabon 1
GD - Grenada 1
GY - Guiana 1
HN - Honduras 1
KE - Kenya 1
LB - Libano 1
MD - Moldavia 1
MN - Mongolia 1
NO - Norvegia 1
NP - Nepal 1
OM - Oman 1
QA - Qatar 1
SC - Seychelles 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
TL - Timor Orientale 1
Totale 20.393
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Città #
Wilmington 3.641
Woodbridge 3.454
Houston 2.892
Singapore 574
Ashburn 480
Fairfield 409
San Jose 383
Chandler 366
Ann Arbor 347
Beijing 195
Seattle 192
Hong Kong 186
Council Bluffs 171
Dublin 160
Rome 158
Jacksonville 135
Cambridge 132
Medford 118
New York 109
Santa Clara 108
Dearborn 96
Los Angeles 94
The Dalles 85
Helsinki 80
Munich 58
Lawrence 54
Tokyo 54
Ho Chi Minh City 49
Buffalo 46
Lauterbourg 43
Dallas 42
Hanoi 41
Denver 40
Milan 39
Phoenix 39
Chicago 38
Moscow 35
San Diego 35
São Paulo 33
Brussels 32
Menlo Park 32
Orem 25
London 23
Naples 23
Warsaw 22
Brooklyn 21
Nuremberg 20
Atlanta 19
Frankfurt am Main 18
Salt Lake City 18
Montreal 17
Zhengzhou 17
Chennai 16
Hefei 16
Nanjing 16
Toronto 16
Engelhard 14
Florence 14
Mülheim 14
North Bergen 14
Pune 14
San Mateo 14
Amsterdam 13
Jakarta 13
Monte Vista 13
Poplar 13
Redondo Beach 13
San Francisco 13
Bologna 11
Catania 11
Redwood City 11
Seoul 11
Stockholm 11
Barcelona 10
Shanghai 10
Boardman 9
Da Nang 9
Miami 9
Norwalk 9
St. George 9
Brasília 8
Center 8
Guangzhou 8
Rio de Janeiro 8
Tampa 8
University Park 8
Verona 8
Washington 8
Ardabil 7
Brno 7
City of London 7
Johannesburg 7
Kraków 7
Manchester 7
Palermo 7
Philadelphia 7
Turku 7
Columbus 6
Creede 6
Hangzhou 6
Totale 15.989
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Nome #
Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency 555
Chronic Granulomatous Disease Presenting with Salmonella Brain Abscesses. 513
Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy 501
Dual-regulated lentiviral vector for gene therapy of X-linked chronic granulomatosis 500
Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: An Italian multicenter study 498
Early-onset monocyte-B-natural killer-dendritic cells' deficiency successfully treated with hematopoietic stem cell transplantation. 496
A variable degree of autoimmunity in the pedigree of a patient with type 1 diabetes homozygous for the PTPN22 1858T variant 480
Visceral leishmaniasis revealing chronic granulomatous diseases in a child 478
The impact of TACI mutations: from hypogammaglobulinemia in infancy to autoimmunity in adulthood 477
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 477
Dysplasia of Granulocytes in a Patient with HPV Disease, Recurrent Infections, and B Lymphopenia: A Novel Variant of WHIM Syndrome? 472
A Familiar CD4 Lymphopenia? 471
CD4 linfocitopenia di padre in figlio: cammino obbligato verso una ipogammaglobulinemia? 471
. Early-onset monocyte-B-natural killer-dendritic cells’ deficiency successfully treated with hematopoietic stem cell transaplantation 465
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. 454
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). 443
The impact of TACI mutations in children affected with hypogammaglobulinemia and in their relatives with autoimmunity: a matter of age. 438
Combined immunodeficiency due to JAK3 mutation in a child presenting with skin granuloma 436
Successful treatment with percutaneous transhepatic alcoholization of a liver abscess in a child with chronic granulomatous disease 435
Defective B-cell proliferation and maintenance of long-term memory in patients with chronic granulomatous disease 433
Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience 411
Serratia marcescens Osteomyelitis in a Newborn with Chronic Granulomatous 409
Caratterizzazione clinica di pazienti con ipogammaglobulinemia. 403
Clinical characterization of hypogammaglobulinemia. 402
Identification of a Btk mutation in a dysgammaglobulinemic patient with reduced B cells: XLA diagnosis or not? 397
Insight into B-cell development and differentiation 388
Molecular characterization of TNFRSF13B gene in pediatric patients with hypogammaglobulinemia. 382
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 378
Functional analysis of peripheral blood B cells in a case of atypical XLA 376
Late-onset combined immune-deficiency due to LIGIV mutations in a 12 years old patient 364
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 343
Dual response to human papilloma virus vaccine in an immunodeficiency disorder: Resolution of plantar warts and persistence of condylomas 337
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. 325
The dilemma of PID diagnosis. The identification of a BTK mutation is not sufficient to TAG a disease. 298
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 292
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 275
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children 270
First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia 248
The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment 245
Impaired X-CGD T cell compartment is gp91phox-NADPH oxidase independent 234
Diagnostic Approach to Monogenic Inflammatory Bowel Disease in Clinical Practice: A Ten-Year Multicentric Experience 223
Urogenital Abnormalities in Adenosine Deaminase Deficiency 217
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) 214
Molecular characterization and novel mutations in a large cohort of patients with chronic granulomatous disease 213
Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child with Intermittent Neutropenia 209
Clinical, immunological, and functional characterization of six patients with very high IgM levels 208
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 206
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. 205
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection 195
Clinical, Immunological, and Molecular Variability of RAG Deficiency: A Retrospective Analysis of 22 RAG Patients 156
Partial T cell defects and expanded CD56bright NK cells in an SCID patient carrying hypomorphic mutation in the IL2RG gene 148
Altered NK-cell compartment and dysfunctional NKG2D/NKG2D-ligand axis in patients with ataxia-telangiectasia 144
The Evolutionary Scenario of Pediatric Unclassified Primary Antibody Deficiency to Adulthood 142
IPINeT Ped-unPAD Study: Goals, Design, and Preliminary Results 133
Case Report: EBV Chronic Infection and Lymphoproliferation in Four APDS Patients: The Challenge of Proper Characterization, Therapy, and Follow-Up 130
Immunological aspects of x-linked chronic granulomatous disease female carriers 116
Case Report: Altered NK Cell Compartment and Reduced CXCR4 Chemotactic Response of B Lymphocytes in an Immunodeficient Patient With HPV-Related Disease 115
Humoral and cellular response following vaccination with the BNT162b2 mRNA COVID-19 vaccine in patients affected by primary immunodeficiencies 115
Case Report: Crossing a rugged road in a primary immune regulatory disorder 109
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease 106
Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait? 105
Case report: Neonatal-onset inflammatory bowel disease due to novel compound heterozygous mutations in DUOX2 104
Gastric cancer, inflammatory bowel disease and polyautoimmunity in a 17-year-old boy: CTLA-4 deficiency successfully treated with Abatacept 102
Characterization of AR-CGD female patient with a novel homozygous deletion in CYBC1 gene presenting with unusual clinical phenotype 99
Cohen syndrome and neutropenia: Unveiling a novel VPS13B variant and literature review 92
Corrigendum: Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult Patient 77
Natural history of type 1 diabetes on an immunodysregulatory background with genetic alteration in B-cell activating factor receptor: A case report 75
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 72
Corrigendum to: Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency 65
Partial Loss of NEMO Function in a Female Carrier with No Incontinentia Pigmenti 63
TNFRSF13B genetic characterization of pediatric patients with hypogammaglobulinemia. 62
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for diagnosing inborn errors of immunity 33
Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature 31
The dilemma of X-linked agammaglobulinemia carriers 30
Refractory immune cytopenia successfully treated with mycophenolate mofetil in four adolescents with del22q11.2 syndrome. 27
Lymphoproliferation in inborn errors of immunity: From challenging diagnosis to histologic revision 25
Inherited deficiency of DIAPH1 identifies a DNA double strand break repair pathway regulated by γ-actin 23
Totale 20.659
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Categoria #
all - tutte 56.290
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 56.290
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022543 0 0 0 35 86 53 20 38 69 38 42 162
2022/2023908 89 91 44 107 58 208 102 73 67 4 48 17
2023/2024396 45 39 13 21 46 97 13 20 26 6 1 69
2024/20251.733 56 359 169 115 72 125 158 96 164 148 192 79
2025/20263.180 257 144 279 346 326 107 406 306 388 301 208 112
2026/20271.169 283 202 495 189 0 0 0 0 0 0 0 0
Totale 20.659