IRIS
DI MATTEO, GIGLIOLA
 Distribuzione geografica
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Continente #
NA - Nord America 14.491
EU - Europa 2.358
AS - Asia 2.102
SA - Sud America 321
AF - Africa 31
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 19.305
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Nazione #
US - Stati Uniti d'America 14.412
SG - Singapore 912
IT - Italia 553
CN - Cina 443
DE - Germania 403
RU - Federazione Russa 298
BR - Brasile 261
FR - Francia 190
IE - Irlanda 190
HK - Hong Kong 187
VN - Vietnam 171
UA - Ucraina 164
GB - Regno Unito 135
FI - Finlandia 124
BD - Bangladesh 93
SE - Svezia 81
JP - Giappone 61
NL - Olanda 56
CA - Canada 51
IN - India 51
KR - Corea 47
PL - Polonia 44
BE - Belgio 36
ES - Italia 29
AR - Argentina 22
ID - Indonesia 19
IR - Iran 19
KG - Kirghizistan 19
AT - Austria 16
TR - Turchia 16
MX - Messico 15
CO - Colombia 11
PK - Pakistan 11
ZA - Sudafrica 11
IQ - Iraq 9
CZ - Repubblica Ceca 8
UZ - Uzbekistan 8
CL - Cile 7
CH - Svizzera 6
EC - Ecuador 6
SA - Arabia Saudita 6
EG - Egitto 5
MY - Malesia 5
PH - Filippine 5
PT - Portogallo 5
LT - Lituania 4
PE - Perù 4
AE - Emirati Arabi Uniti 3
BG - Bulgaria 3
JO - Giordania 3
NG - Nigeria 3
PA - Panama 3
PY - Paraguay 3
TN - Tunisia 3
UY - Uruguay 3
VE - Venezuela 3
AO - Angola 2
AZ - Azerbaigian 2
BY - Bielorussia 2
CR - Costa Rica 2
DZ - Algeria 2
GR - Grecia 2
GT - Guatemala 2
HU - Ungheria 2
IL - Israele 2
MA - Marocco 2
PS - Palestinian Territory 2
RO - Romania 2
RS - Serbia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AM - Armenia 1
AU - Australia 1
BZ - Belize 1
DO - Repubblica Dominicana 1
GA - Gabon 1
GD - Grenada 1
GY - Guiana 1
JM - Giamaica 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
SV - El Salvador 1
SY - Repubblica araba siriana 1
TL - Timor Orientale 1
TT - Trinidad e Tobago 1
Totale 19.305
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Città #
Wilmington 3.641
Woodbridge 3.454
Houston 2.891
Singapore 573
Fairfield 409
Ashburn 385
Chandler 366
Ann Arbor 347
San Jose 292
Beijing 192
Seattle 188
Hong Kong 182
Dublin 160
Rome 152
Jacksonville 135
Cambridge 132
Medford 118
Council Bluffs 112
New York 99
Dearborn 96
Santa Clara 95
The Dalles 85
Los Angeles 81
Helsinki 80
Munich 58
Tokyo 54
Lawrence 53
Ho Chi Minh City 49
Lauterbourg 43
Buffalo 41
Hanoi 40
Milan 39
Chicago 35
Moscow 35
San Diego 35
Dallas 33
Menlo Park 32
São Paulo 32
Brussels 31
London 23
Orem 22
Warsaw 22
Nuremberg 20
Phoenix 20
Brooklyn 18
Frankfurt am Main 18
Naples 17
Zhengzhou 17
Atlanta 16
Chennai 16
Hefei 16
Montreal 16
Nanjing 16
Salt Lake City 16
Engelhard 14
Mülheim 14
Pune 14
San Mateo 14
Amsterdam 13
Jakarta 13
Monte Vista 13
North Bergen 13
Poplar 13
Redondo Beach 13
Toronto 12
Florence 11
Redwood City 11
Seoul 11
Stockholm 11
Barcelona 10
Bologna 10
Catania 10
Da Nang 9
Denver 9
Shanghai 9
St. George 9
Boardman 8
Center 8
Guangzhou 8
Miami 8
Norwalk 8
Rio de Janeiro 8
University Park 8
Verona 8
Ardabil 7
Brno 7
City of London 7
Johannesburg 7
Kraków 7
Manchester 7
San Francisco 7
Turku 7
Creede 6
Hangzhou 6
Palo Alto 6
Paris 6
Vancouver 6
Wroclaw 6
Brasília 5
Chengdu 5
Totale 15.570
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Nome #
Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency 536
Chronic Granulomatous Disease Presenting with Salmonella Brain Abscesses. 502
Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy 489
Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: An Italian multicenter study 486
Dual-regulated lentiviral vector for gene therapy of X-linked chronic granulomatosis 485
Early-onset monocyte-B-natural killer-dendritic cells' deficiency successfully treated with hematopoietic stem cell transplantation. 478
A variable degree of autoimmunity in the pedigree of a patient with type 1 diabetes homozygous for the PTPN22 1858T variant 470
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 469
The impact of TACI mutations: from hypogammaglobulinemia in infancy to autoimmunity in adulthood 464
A Familiar CD4 Lymphopenia? 463
Visceral leishmaniasis revealing chronic granulomatous diseases in a child 462
CD4 linfocitopenia di padre in figlio: cammino obbligato verso una ipogammaglobulinemia? 454
. Early-onset monocyte-B-natural killer-dendritic cells’ deficiency successfully treated with hematopoietic stem cell transaplantation 454
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. 442
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). 426
Successful treatment with percutaneous transhepatic alcoholization of a liver abscess in a child with chronic granulomatous disease 423
The impact of TACI mutations in children affected with hypogammaglobulinemia and in their relatives with autoimmunity: a matter of age. 423
Combined immunodeficiency due to JAK3 mutation in a child presenting with skin granuloma 423
Defective B-cell proliferation and maintenance of long-term memory in patients with chronic granulomatous disease 422
Dysplasia of Granulocytes in a Patient with HPV Disease, Recurrent Infections, and B Lymphopenia: A Novel Variant of WHIM Syndrome? 413
Serratia marcescens Osteomyelitis in a Newborn with Chronic Granulomatous 406
Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience 404
Clinical characterization of hypogammaglobulinemia. 394
Caratterizzazione clinica di pazienti con ipogammaglobulinemia. 385
Identification of a Btk mutation in a dysgammaglobulinemic patient with reduced B cells: XLA diagnosis or not? 381
Insight into B-cell development and differentiation 373
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 369
Molecular characterization of TNFRSF13B gene in pediatric patients with hypogammaglobulinemia. 369
Functional analysis of peripheral blood B cells in a case of atypical XLA 365
Late-onset combined immune-deficiency due to LIGIV mutations in a 12 years old patient 353
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 326
Dual response to human papilloma virus vaccine in an immunodeficiency disorder: Resolution of plantar warts and persistence of condylomas 321
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. 318
The dilemma of PID diagnosis. The identification of a BTK mutation is not sufficient to TAG a disease. 285
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 281
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 257
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children 250
The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment 235
First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia 234
Impaired X-CGD T cell compartment is gp91phox-NADPH oxidase independent 219
Diagnostic Approach to Monogenic Inflammatory Bowel Disease in Clinical Practice: A Ten-Year Multicentric Experience 211
Urogenital Abnormalities in Adenosine Deaminase Deficiency 202
Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child with Intermittent Neutropenia 199
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 197
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) 196
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. 195
Clinical, immunological, and functional characterization of six patients with very high IgM levels 189
Molecular characterization and novel mutations in a large cohort of patients with chronic granulomatous disease 187
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection 184
Partial T cell defects and expanded CD56bright NK cells in an SCID patient carrying hypomorphic mutation in the IL2RG gene 136
Clinical, Immunological, and Molecular Variability of RAG Deficiency: A Retrospective Analysis of 22 RAG Patients 135
Altered NK-cell compartment and dysfunctional NKG2D/NKG2D-ligand axis in patients with ataxia-telangiectasia 130
The Evolutionary Scenario of Pediatric Unclassified Primary Antibody Deficiency to Adulthood 126
IPINeT Ped-unPAD Study: Goals, Design, and Preliminary Results 120
Case Report: EBV Chronic Infection and Lymphoproliferation in Four APDS Patients: The Challenge of Proper Characterization, Therapy, and Follow-Up 119
Immunological aspects of x-linked chronic granulomatous disease female carriers 108
Case Report: Altered NK Cell Compartment and Reduced CXCR4 Chemotactic Response of B Lymphocytes in an Immunodeficient Patient With HPV-Related Disease 101
Humoral and cellular response following vaccination with the BNT162b2 mRNA COVID-19 vaccine in patients affected by primary immunodeficiencies 100
Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait? 97
Case Report: Crossing a rugged road in a primary immune regulatory disorder 93
Gastric cancer, inflammatory bowel disease and polyautoimmunity in a 17-year-old boy: CTLA-4 deficiency successfully treated with Abatacept 92
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease 92
Characterization of AR-CGD female patient with a novel homozygous deletion in CYBC1 gene presenting with unusual clinical phenotype 88
Case report: Neonatal-onset inflammatory bowel disease due to novel compound heterozygous mutations in DUOX2 83
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 67
Corrigendum: Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult Patient 67
Natural history of type 1 diabetes on an immunodysregulatory background with genetic alteration in B-cell activating factor receptor: A case report 64
Cohen syndrome and neutropenia: Unveiling a novel VPS13B variant and literature review 56
Corrigendum to: Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency 55
TNFRSF13B genetic characterization of pediatric patients with hypogammaglobulinemia. 52
Partial Loss of NEMO Function in a Female Carrier with No Incontinentia Pigmenti 42
The dilemma of X-linked agammaglobulinemia carriers 18
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for diagnosing inborn errors of immunity 15
Refractory immune cytopenia successfully treated with mycophenolate mofetil in four adolescents with del22q11.2 syndrome. 13
Lymphoproliferation in inborn errors of immunity: From challenging diagnosis to histologic revision 12
Inherited deficiency of DIAPH1 identifies a DNA double strand break repair pathway regulated by γ-actin 11
Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature 10
Totale 19.571
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Categoria #
all - tutte 52.198
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 52.198
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022669 27 73 26 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
2026/202781 81 0 0 0 0 0 0 0 0 0 0 0
Totale 19.571