IRIS
DI MATTEO, GIGLIOLA
 Distribuzione geografica
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Continente #
NA - Nord America 13.770
EU - Europa 1.589
AS - Asia 729
SA - Sud America 10
AF - Africa 4
Continente sconosciuto - Info sul continente non disponibili 1
Totale 16.103
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Nazione #
US - Stati Uniti d'America 13.763
SG - Singapore 373
DE - Germania 350
IT - Italia 331
CN - Cina 210
IE - Irlanda 201
UA - Ucraina 171
RU - Federazione Russa 129
FR - Francia 115
GB - Regno Unito 86
SE - Svezia 71
KR - Corea 48
FI - Finlandia 47
BE - Belgio 35
IN - India 25
KG - Kirghizistan 20
NL - Olanda 14
PL - Polonia 14
IR - Iran 13
HK - Hong Kong 9
CZ - Repubblica Ceca 8
JP - Giappone 8
TR - Turchia 6
VN - Vietnam 6
BR - Brasile 5
CA - Canada 5
CH - Svizzera 5
PT - Portogallo 4
CL - Cile 3
AT - Austria 2
ES - Italia 2
PK - Pakistan 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
AR - Argentina 1
BD - Bangladesh 1
BG - Bulgaria 1
BZ - Belize 1
EG - Egitto 1
HU - Ungheria 1
ID - Indonesia 1
IL - Israele 1
MN - Mongolia 1
MX - Messico 1
NG - Nigeria 1
NO - Norvegia 1
PE - Perù 1
PH - Filippine 1
QA - Qatar 1
RO - Romania 1
SA - Arabia Saudita 1
SC - Seychelles 1
TN - Tunisia 1
UZ - Uzbekistan 1
Totale 16.103
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Città #
Wilmington 3.870
Woodbridge 3.688
Houston 3.077
Fairfield 449
Chandler 382
Ann Arbor 359
Singapore 333
Ashburn 245
Seattle 194
Dublin 168
Cambridge 145
Jacksonville 141
Medford 126
Rome 115
Dearborn 108
Beijing 96
Santa Clara 83
Lawrence 57
New York 57
San Diego 37
Menlo Park 33
Munich 32
Brussels 31
Milan 23
Moscow 17
Nanjing 17
Zhengzhou 17
Hefei 15
Mülheim 15
Engelhard 14
Pune 14
San Mateo 14
London 13
Helsinki 12
Redwood City 12
Seoul 11
Norwalk 9
St. George 9
Verona 9
Brno 8
Center 8
Hong Kong 8
Shanghai 8
University Park 8
Ardabil 7
Boardman 7
Kraków 7
Palo Alto 7
Creede 6
Phoenix 6
Amsterdam 5
Council Bluffs 5
Dong Ket 5
Florence 5
Hangzhou 5
Kunming 5
Mountain View 5
Nanchang 5
Palermo 5
Radomsko 5
Augusta 4
Cagliari 4
Chengdu 4
Guangzhou 4
Jinan 4
Los Angeles 4
Nürnberg 4
São Paulo 4
Toronto 4
Waanrode 4
Bologna 3
Changsha 3
Falls Church 3
Genoa 3
Kilburn 3
Lonato 3
Prescot 3
Salt Lake City 3
San Francisco 3
Shenyang 3
Tokyo 3
Trento 3
Trieste 3
Ypsilanti 3
Acton 2
Casalecchio di Reno 2
Catania 2
Chiswick 2
Cisterna Di Latina 2
Del Norte 2
Denver 2
Fabbrico 2
Ferrara di Monte Baldo 2
Guidonia 2
Hounslow 2
Indiana 2
Islamabad 2
Lappeenranta 2
Leawood 2
Macerata 2
Totale 14.291
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Nome #
Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency 443
Chronic Granulomatous Disease Presenting with Salmonella Brain Abscesses. 440
Pancytopenia and severe sepsis in an adult case of congenital X-linked agammaglobulinemia (XLA) 434
Dual-regulated lentiviral vector for gene therapy of X-linked chronic granulomatosis 430
Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: An Italian multicenter study 427
Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy 425
Early-onset monocyte-B-natural killer-dendritic cells' deficiency successfully treated with hematopoietic stem cell transplantation. 422
The impact of TACI mutations: from hypogammaglobulinemia in infancy to autoimmunity in adulthood 411
Visceral leishmaniasis revealing chronic granulomatous diseases in a child 409
A case of APDS patient: defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment 401
CD4 linfocitopenia di padre in figlio: cammino obbligato verso una ipogammaglobulinemia? 396
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 396
. Early-onset monocyte-B-natural killer-dendritic cells’ deficiency successfully treated with hematopoietic stem cell transaplantation 391
Combined immunodeficiency due to JAK3 mutation in a child presenting with skin granuloma 387
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. 386
A variable degree of autoimmunity in the pedigree of a patient with type 1 diabetes homozygous for the PTPN22 1858T variant 386
Successful treatment with percutaneous transhepatic alcoholization of a liver abscess in a child with chronic granulomatous disease 383
The impact of TACI mutations in children affected with hypogammaglobulinemia and in their relatives with autoimmunity: a matter of age. 381
Defective B-cell proliferation and maintenance of long-term memory in patients with chronic granulomatous disease 380
A Familiar CD4 Lymphopenia? 379
Serratia marcescens Osteomyelitis in a Newborn with Chronic Granulomatous 371
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). 366
Dysplasia of Granulocytes in a Patient with HPV Disease, Recurrent Infections, and B Lymphopenia: A Novel Variant of WHIM Syndrome? 353
Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience 348
Identification of a Btk mutation in a dysgammaglobulinemic patient with reduced B cells: XLA diagnosis or not? 334
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 332
Insight into B-cell development and differentiation 331
Functional analysis of peripheral blood B cells in a case of atypical XLA 331
Clinical characterization of hypogammaglobulinemia. 327
Molecular characterization of TNFRSF13B gene in pediatric patients with hypogammaglobulinemia. 325
Late-onset combined immune-deficiency due to LIGIV mutations in a 12 years old patient 310
Caratterizzazione clinica di pazienti con ipogammaglobulinemia. 308
Dual response to human papilloma virus vaccine in an immunodeficiency disorder: Resolution of plantar warts and persistence of condylomas 290
The dilemma of PID diagnosis. The identification of a BTK mutation is not sufficient to TAG a disease. 256
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 248
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. 246
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children 213
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 179
Impaired X-CGD T cell compartment is gp91phox-NADPH oxidase independent 175
First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia 165
The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment 164
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 161
Diagnostic Approach to Monogenic Inflammatory Bowel Disease in Clinical Practice: A Ten-Year Multicentric Experience 158
Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child with Intermittent Neutropenia 150
Clinical, immunological, and functional characterization of six patients with very high IgM levels 147
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 146
Urogenital Abnormalities in Adenosine Deaminase Deficiency 144
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. 144
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection 144
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) 136
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 128
Molecular characterization and novel mutations in a large cohort of patients with chronic granulomatous disease 117
Partial T cell defects and expanded CD56bright NK cells in an SCID patient carrying hypomorphic mutation in the IL2RG gene 89
Clinical, Immunological, and Molecular Variability of RAG Deficiency: A Retrospective Analysis of 22 RAG Patients 68
Case Report: EBV Chronic Infection and Lymphoproliferation in Four APDS Patients: The Challenge of Proper Characterization, Therapy, and Follow-Up 65
Immunological aspects of x-linked chronic granulomatous disease female carriers 54
Altered NK-cell compartment and dysfunctional NKG2D/NKG2D-ligand axis in patients with ataxia-telangiectasia 49
Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature 38
The Evolutionary Scenario of Pediatric Unclassified Primary Antibody Deficiency to Adulthood 34
Humoral and cellular response following vaccination with the BNT162b2 mRNA COVID-19 vaccine in patients affected by primary immunodeficiencies 34
Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait? 33
Gastric cancer, inflammatory bowel disease and polyautoimmunity in a 17-year-old boy: CTLA-4 deficiency successfully treated with Abatacept 32
TNFRSF13B genetic characterization of pediatric patients with hypogammaglobulinemia. 26
Case Report: Altered NK Cell Compartment and Reduced CXCR4 Chemotactic Response of B Lymphocytes in an Immunodeficient Patient With HPV-Related Disease 24
Corrigendum: Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult Patient 24
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 22
Natural history of type 1 diabetes on an immunodysregulatory background with genetic alteration in B-cell activating factor receptor: A case report 20
Characterization of AR-CGD female patient with a novel homozygous deletion in CYBC1 gene presenting with unusual clinical phenotype 20
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease 16
Corrigendum to: Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency 15
Case Report: Crossing a rugged road in a primary immune regulatory disorder 14
Case report: Neonatal-onset inflammatory bowel disease due to novel compound heterozygous mutations in DUOX2 12
Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience 11
Totale 16.354
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Categoria #
all - tutte 37.609
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 37.609
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.906 0 0 0 0 298 372 374 361 436 415 319 331
2020/20213.058 326 343 303 355 316 319 392 359 132 85 97 31
2021/2022721 28 76 28 38 88 60 23 38 82 41 45 174
2022/2023951 94 95 45 111 60 221 106 79 67 4 50 19
2023/2024416 48 39 16 22 50 101 13 21 27 8 1 70
2024/2025833 61 391 191 123 67 0 0 0 0 0 0 0
Totale 16.354