DI MATTEO, GIGLIOLA
 Distribuzione geografica
Continente #
NA - Nord America 14.352
EU - Europa 2.331
AS - Asia 2.085
SA - Sud America 329
AF - Africa 32
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 19.131
Nazione #
US - Stati Uniti d'America 14.279
SG - Singapore 947
IT - Italia 506
CN - Cina 448
DE - Germania 406
RU - Federazione Russa 303
BR - Brasile 265
HK - Hong Kong 197
IE - Irlanda 193
FR - Francia 192
VN - Vietnam 170
UA - Ucraina 164
GB - Regno Unito 137
FI - Finlandia 125
SE - Svezia 81
JP - Giappone 63
NL - Olanda 58
IN - India 54
KR - Corea 47
PL - Polonia 45
CA - Canada 44
BE - Belgio 36
ES - Italia 29
AR - Argentina 24
BD - Bangladesh 22
IR - Iran 19
KG - Kirghizistan 19
ID - Indonesia 18
MX - Messico 17
AT - Austria 16
TR - Turchia 16
CO - Colombia 11
PK - Pakistan 11
ZA - Sudafrica 11
IQ - Iraq 9
CZ - Repubblica Ceca 8
UZ - Uzbekistan 8
CL - Cile 7
EC - Ecuador 7
SA - Arabia Saudita 7
CH - Svizzera 6
EG - Egitto 5
MY - Malesia 5
PH - Filippine 5
PT - Portogallo 5
BG - Bulgaria 4
LT - Lituania 4
PE - Perù 4
PY - Paraguay 4
TN - Tunisia 4
AE - Emirati Arabi Uniti 3
JO - Giordania 3
NG - Nigeria 3
PA - Panama 3
UY - Uruguay 3
VE - Venezuela 3
AO - Angola 2
AZ - Azerbaigian 2
BY - Bielorussia 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
GR - Grecia 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
GA - Gabon 1
GD - Grenada 1
GT - Guatemala 1
GY - Guiana 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 19.131
Città #
Wilmington 3.642
Woodbridge 3.454
Houston 2.891
Singapore 598
Fairfield 412
Ashburn 368
Chandler 366
Ann Arbor 347
San Jose 285
Beijing 195
Hong Kong 193
Seattle 187
Dublin 163
Rome 146
Jacksonville 135
Cambridge 131
Medford 120
Dearborn 96
New York 93
Santa Clara 90
The Dalles 88
Helsinki 80
Los Angeles 80
Council Bluffs 72
Munich 60
Tokyo 56
Lawrence 54
Ho Chi Minh City 49
Lauterbourg 44
Buffalo 38
Hanoi 38
Moscow 35
San Diego 35
Milan 34
Chicago 33
Menlo Park 32
Brussels 31
São Paulo 31
Dallas 27
Orem 24
London 23
Warsaw 22
Nuremberg 21
Frankfurt am Main 18
Phoenix 18
Brooklyn 17
Chennai 17
Zhengzhou 17
Atlanta 16
Hefei 16
Nanjing 16
Salt Lake City 16
Montreal 15
Engelhard 14
Mülheim 14
North Bergen 14
Pune 14
Redondo Beach 14
San Mateo 14
Amsterdam 13
Jakarta 13
Poplar 13
Naples 12
Redwood City 11
Seoul 11
Stockholm 11
Barcelona 10
Florence 10
Bologna 9
Catania 9
Da Nang 9
Denver 9
Rio de Janeiro 9
Shanghai 9
St. George 9
Toronto 9
Boardman 8
Center 8
City of London 8
Guangzhou 8
Miami 8
Norwalk 8
Turku 8
University Park 8
Verona 8
Ardabil 7
Brno 7
Johannesburg 7
Kraków 7
Manchester 7
San Francisco 7
Wroclaw 7
Creede 6
Hangzhou 6
Mumbai 6
Palo Alto 6
Paris 6
Vancouver 6
Brasília 5
Chengdu 5
Totale 15.512
Nome #
Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency 529
Chronic Granulomatous Disease Presenting with Salmonella Brain Abscesses. 496
Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy 487
Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: An Italian multicenter study 483
Dual-regulated lentiviral vector for gene therapy of X-linked chronic granulomatosis 477
Early-onset monocyte-B-natural killer-dendritic cells' deficiency successfully treated with hematopoietic stem cell transplantation. 476
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 467
A variable degree of autoimmunity in the pedigree of a patient with type 1 diabetes homozygous for the PTPN22 1858T variant 466
A Familiar CD4 Lymphopenia? 463
Visceral leishmaniasis revealing chronic granulomatous diseases in a child 462
The impact of TACI mutations: from hypogammaglobulinemia in infancy to autoimmunity in adulthood 461
. Early-onset monocyte-B-natural killer-dendritic cells’ deficiency successfully treated with hematopoietic stem cell transaplantation 454
CD4 linfocitopenia di padre in figlio: cammino obbligato verso una ipogammaglobulinemia? 453
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. 439
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). 424
Successful treatment with percutaneous transhepatic alcoholization of a liver abscess in a child with chronic granulomatous disease 423
Combined immunodeficiency due to JAK3 mutation in a child presenting with skin granuloma 423
The impact of TACI mutations in children affected with hypogammaglobulinemia and in their relatives with autoimmunity: a matter of age. 421
Defective B-cell proliferation and maintenance of long-term memory in patients with chronic granulomatous disease 417
Dysplasia of Granulocytes in a Patient with HPV Disease, Recurrent Infections, and B Lymphopenia: A Novel Variant of WHIM Syndrome? 411
Serratia marcescens Osteomyelitis in a Newborn with Chronic Granulomatous 404
Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience 403
Clinical characterization of hypogammaglobulinemia. 383
Caratterizzazione clinica di pazienti con ipogammaglobulinemia. 382
Identification of a Btk mutation in a dysgammaglobulinemic patient with reduced B cells: XLA diagnosis or not? 379
Insight into B-cell development and differentiation 369
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 368
Molecular characterization of TNFRSF13B gene in pediatric patients with hypogammaglobulinemia. 368
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 351
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 321
Dual response to human papilloma virus vaccine in an immunodeficiency disorder: Resolution of plantar warts and persistence of condylomas 320
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. 315
The dilemma of PID diagnosis. The identification of a BTK mutation is not sufficient to TAG a disease. 284
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 280
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children 248
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 246
First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia 232
The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment 226
Impaired X-CGD T cell compartment is gp91phox-NADPH oxidase independent 214
Diagnostic Approach to Monogenic Inflammatory Bowel Disease in Clinical Practice: A Ten-Year Multicentric Experience 210
Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child with Intermittent Neutropenia 198
Urogenital Abnormalities in Adenosine Deaminase Deficiency 198
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) 195
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 192
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. 191
Clinical, immunological, and functional characterization of six patients with very high IgM levels 185
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection 181
Molecular characterization and novel mutations in a large cohort of patients with chronic granulomatous disease 179
Partial T cell defects and expanded CD56bright NK cells in an SCID patient carrying hypomorphic mutation in the IL2RG gene 133
Clinical, Immunological, and Molecular Variability of RAG Deficiency: A Retrospective Analysis of 22 RAG Patients 132
Altered NK-cell compartment and dysfunctional NKG2D/NKG2D-ligand axis in patients with ataxia-telangiectasia 126
The Evolutionary Scenario of Pediatric Unclassified Primary Antibody Deficiency to Adulthood 117
Case Report: EBV Chronic Infection and Lymphoproliferation in Four APDS Patients: The Challenge of Proper Characterization, Therapy, and Follow-Up 113
IPINeT Ped-unPAD Study: Goals, Design, and Preliminary Results 112
Immunological aspects of x-linked chronic granulomatous disease female carriers 101
Case Report: Altered NK Cell Compartment and Reduced CXCR4 Chemotactic Response of B Lymphocytes in an Immunodeficient Patient With HPV-Related Disease 97
Humoral and cellular response following vaccination with the BNT162b2 mRNA COVID-19 vaccine in patients affected by primary immunodeficiencies 94
Case Report: Crossing a rugged road in a primary immune regulatory disorder 93
Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait? 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
Gastric cancer, inflammatory bowel disease and polyautoimmunity in a 17-year-old boy: CTLA-4 deficiency successfully treated with Abatacept 87
Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature 77
Case report: Neonatal-onset inflammatory bowel disease due to novel compound heterozygous mutations in DUOX2 74
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for the diagnosis of inborn errors of immunity (IEI) 71
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 66
Natural history of type 1 diabetes on an immunodysregulatory background with genetic alteration in B-cell activating factor receptor: A case report 61
Corrigendum to: Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency 50
TNFRSF13B genetic characterization of pediatric patients with hypogammaglobulinemia. 50
Cohen syndrome and neutropenia: Unveiling a novel VPS13B variant and literature review 44
Partial Loss of NEMO Function in a Female Carrier with No Incontinentia Pigmenti 29
Totale 19.385
Categoria #
all - tutte 50.608
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 50.608


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021122 0 0 0 0 0 0 0 0 0 0 92 30
2021/2022682 27 73 26 35 86 57 21 38 74 38 42 165
2022/2023912 90 91 44 107 58 210 103 73 67 4 48 17
2023/2024400 45 39 14 22 46 97 13 20 27 7 1 69
2024/20251.788 57 367 176 116 72 137 162 96 165 160 198 82
2025/20262.999 264 148 287 354 334 109 412 316 401 306 68 0
Totale 19.385