IRIS
DI MATTEO, GIGLIOLA
 Distribuzione geografica
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Continente #
NA - Nord America 13.452
EU - Europa 1.397
AS - Asia 348
SA - Sud America 10
AF - Africa 4
Continente sconosciuto - Info sul continente non disponibili 1
Totale 15.212
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Nazione #
US - Stati Uniti d'America 13.446
DE - Germania 316
IT - Italia 285
CN - Cina 205
IE - Irlanda 200
UA - Ucraina 171
FR - Francia 115
GB - Regno Unito 83
SE - Svezia 71
RU - Federazione Russa 48
KR - Corea 47
BE - Belgio 35
FI - Finlandia 35
IN - India 25
KG - Kirghizistan 20
PL - Polonia 14
IR - Iran 13
HK - Hong Kong 9
JP - Giappone 8
NL - Olanda 7
VN - Vietnam 6
BR - Brasile 5
CH - Svizzera 5
TR - Turchia 5
CA - Canada 4
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
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 15.212
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Città #
Wilmington 3.870
Woodbridge 3.688
Houston 3.077
Fairfield 449
Chandler 382
Ann Arbor 359
Ashburn 237
Seattle 194
Dublin 167
Cambridge 145
Jacksonville 141
Medford 126
Dearborn 108
Rome 101
Beijing 96
Lawrence 57
New York 55
San Diego 37
Menlo Park 33
Brussels 31
Milan 19
Nanjing 17
Zhengzhou 16
Hefei 15
Mülheim 15
Engelhard 14
Pune 14
San Mateo 14
London 12
Redwood City 12
Seoul 11
Norwalk 9
St. George 9
Verona 9
Center 8
Hong Kong 8
University Park 8
Ardabil 7
Kraków 7
Palo Alto 7
Shanghai 7
Creede 6
Dong Ket 5
Florence 5
Hangzhou 5
Kunming 5
Mountain View 5
Nanchang 5
Palermo 5
Phoenix 5
Radomsko 5
Augusta 4
Boardman 4
Cagliari 4
Chengdu 4
Guangzhou 4
Jinan 4
Nürnberg 4
São Paulo 4
Toronto 4
Waanrode 4
Bologna 3
Changsha 3
Falls Church 3
Genoa 3
Kilburn 3
Lonato 3
Los Angeles 3
Prescot 3
San Francisco 3
Santa Clara 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
Fabbrico 2
Ferrara di Monte Baldo 2
Guidonia 2
Hounslow 2
Indiana 2
Islamabad 2
Leawood 2
Macerata 2
Madrid 2
Minusio 2
Monte Vista 2
Naples 2
Odivelas 2
Perugia 2
Pontecchio Polesine 2
Porto 2
Quzhou 2
Redmond 2
Totale 13.775
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Nome #
Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency 433
Chronic Granulomatous Disease Presenting with Salmonella Brain Abscesses. 426
Dual-regulated lentiviral vector for gene therapy of X-linked chronic granulomatosis 423
Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: An Italian multicenter study 421
Pancytopenia and severe sepsis in an adult case of congenital X-linked agammaglobulinemia (XLA) 417
Early-onset monocyte-B-natural killer-dendritic cells' deficiency successfully treated with hematopoietic stem cell transplantation. 414
The impact of TACI mutations: from hypogammaglobulinemia in infancy to autoimmunity in adulthood 403
Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy 402
Visceral leishmaniasis revealing chronic granulomatous diseases in a child 395
A case of APDS patient: defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment 393
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 392
CD4 linfocitopenia di padre in figlio: cammino obbligato verso una ipogammaglobulinemia? 384
Combined immunodeficiency due to JAK3 mutation in a child presenting with skin granuloma 379
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. 377
. Early-onset monocyte-B-natural killer-dendritic cells’ deficiency successfully treated with hematopoietic stem cell transaplantation 375
Successful treatment with percutaneous transhepatic alcoholization of a liver abscess in a child with chronic granulomatous disease 373
Defective B-cell proliferation and maintenance of long-term memory in patients with chronic granulomatous disease 372
A variable degree of autoimmunity in the pedigree of a patient with type 1 diabetes homozygous for the PTPN22 1858T variant 370
A Familiar CD4 Lymphopenia? 370
The impact of TACI mutations in children affected with hypogammaglobulinemia and in their relatives with autoimmunity: a matter of age. 369
Serratia marcescens Osteomyelitis in a Newborn with Chronic Granulomatous 368
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). 349
Dysplasia of Granulocytes in a Patient with HPV Disease, Recurrent Infections, and B Lymphopenia: A Novel Variant of WHIM Syndrome? 337
Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience 332
Identification of a Btk mutation in a dysgammaglobulinemic patient with reduced B cells: XLA diagnosis or not? 327
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 327
Insight into B-cell development and differentiation 324
Clinical characterization of hypogammaglobulinemia. 318
Functional analysis of peripheral blood B cells in a case of atypical XLA 315
Molecular characterization of TNFRSF13B gene in pediatric patients with hypogammaglobulinemia. 315
Late-onset combined immune-deficiency due to LIGIV mutations in a 12 years old patient 292
Caratterizzazione clinica di pazienti con ipogammaglobulinemia. 290
Dual response to human papilloma virus vaccine in an immunodeficiency disorder: Resolution of plantar warts and persistence of condylomas 282
The dilemma of PID diagnosis. The identification of a BTK mutation is not sufficient to TAG a disease. 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. 236
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 231
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children 206
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 170
Impaired X-CGD T cell compartment is gp91phox-NADPH oxidase independent 169
The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment 157
First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia 155
Diagnostic Approach to Monogenic Inflammatory Bowel Disease in Clinical Practice: A Ten-Year Multicentric Experience 150
Urogenital Abnormalities in Adenosine Deaminase Deficiency 138
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 136
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. 136
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection 136
Clinical, immunological, and functional characterization of six patients with very high IgM levels 132
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 129
Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child with Intermittent Neutropenia 129
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 108
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) 108
Molecular characterization and novel mutations in a large cohort of patients with chronic granulomatous disease 101
Partial T cell defects and expanded CD56bright NK cells in an SCID patient carrying hypomorphic mutation in the IL2RG gene 85
Clinical, Immunological, and Molecular Variability of RAG Deficiency: A Retrospective Analysis of 22 RAG Patients 54
Case Report: EBV Chronic Infection and Lymphoproliferation in Four APDS Patients: The Challenge of Proper Characterization, Therapy, and Follow-Up 43
Immunological aspects of x-linked chronic granulomatous disease female carriers 40
Humoral and cellular response following vaccination with the BNT162b2 mRNA COVID-19 vaccine in patients affected by primary immunodeficiencies 29
Altered NK-cell compartment and dysfunctional NKG2D/NKG2D-ligand axis in patients with ataxia-telangiectasia 27
Gastric cancer, inflammatory bowel disease and polyautoimmunity in a 17-year-old boy: CTLA-4 deficiency successfully treated with Abatacept 24
Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature 21
Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait? 18
Natural history of type 1 diabetes on an immunodysregulatory background with genetic alteration in B-cell activating factor receptor: A case report 13
TNFRSF13B genetic characterization of pediatric patients with hypogammaglobulinemia. 13
Corrigendum to: Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency 10
Corrigendum: Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult Patient 9
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 8
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease 7
Characterization of AR-CGD female patient with a novel homozygous deletion in CYBC1 gene presenting with unusual clinical phenotype 6
Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience 4
Totale 15.450
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Categoria #
all - tutte 30.872
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 30.872
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019964 0 0 0 0 0 0 0 0 0 310 317 337
2019/20204.150 301 335 256 352 298 372 374 361 436 415 319 331
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
2023/2024345 48 39 16 22 50 101 13 21 27 8 0 0
Totale 15.450