IRIS
FINOCCHI, ANDREA
 Distribuzione geografica
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Continente #
NA - Nord America 33.429
AS - Asia 4.807
EU - Europa 4.572
SA - Sud America 685
Continente sconosciuto - Info sul continente non disponibili 490
AF - Africa 58
OC - Oceania 23
Totale 44.064
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Nazione #
US - Stati Uniti d'America 33.226
SG - Singapore 2.203
IT - Italia 1.031
CN - Cina 1.001
DE - Germania 752
RU - Federazione Russa 590
BR - Brasile 559
HK - Hong Kong 451
UA - Ucraina 387
IE - Irlanda 378
VN - Vietnam 341
FI - Finlandia 312
FR - Francia 283
SE - Svezia 275
GB - Regno Unito 261
BD - Bangladesh 193
JP - Giappone 129
CA - Canada 111
IN - India 103
KR - Corea 95
NL - Olanda 75
AR - Argentina 54
ID - Indonesia 44
MX - Messico 44
AT - Austria 43
PL - Polonia 42
TR - Turchia 42
ES - Italia 38
IQ - Iraq 36
BE - Belgio 32
KG - Kirghizistan 24
AU - Australia 22
EC - Ecuador 21
CZ - Repubblica Ceca 20
ZA - Sudafrica 20
CO - Colombia 17
IR - Iran 15
SA - Arabia Saudita 15
PH - Filippine 14
PK - Pakistan 14
UZ - Uzbekistan 12
CL - Cile 10
JO - Giordania 10
MY - Malesia 10
KE - Kenya 9
CR - Costa Rica 8
VE - Venezuela 8
EG - Egitto 7
IL - Israele 7
PE - Perù 7
PT - Portogallo 7
AE - Emirati Arabi Uniti 6
CH - Svizzera 6
JM - Giamaica 6
LT - Lituania 6
MA - Marocco 6
TH - Thailandia 6
AZ - Azerbaigian 5
GT - Guatemala 5
PY - Paraguay 5
TT - Trinidad e Tobago 5
TW - Taiwan 5
BG - Bulgaria 4
DZ - Algeria 4
LB - Libano 4
NG - Nigeria 4
NP - Nepal 4
RS - Serbia 4
SV - El Salvador 4
DK - Danimarca 3
EE - Estonia 3
EU - Europa 3
GR - Grecia 3
KZ - Kazakistan 3
MD - Moldavia 3
PA - Panama 3
QA - Qatar 3
RO - Romania 3
SY - Repubblica araba siriana 3
TN - Tunisia 3
AL - Albania 2
BB - Barbados 2
BY - Bielorussia 2
BZ - Belize 2
DM - Dominica 2
DO - Repubblica Dominicana 2
GD - Grenada 2
HN - Honduras 2
HU - Ungheria 2
LV - Lettonia 2
OM - Oman 2
PR - Porto Rico 2
PS - Palestinian Territory 2
SC - Seychelles 2
UY - Uruguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AO - Angola 1
AW - Aruba 1
BH - Bahrain 1
BO - Bolivia 1
Totale 43.565
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Città #
Woodbridge 8.272
Wilmington 7.995
Houston 7.331
Singapore 1.224
Fairfield 1.085
Ashburn 897
Ann Arbor 675
San Jose 652
Chandler 519
Seattle 509
Hong Kong 440
Beijing 398
Cambridge 395
Dublin 351
Jacksonville 346
Council Bluffs 295
Rome 253
Medford 248
Santa Clara 219
Helsinki 211
The Dalles 188
Dearborn 185
New York 179
Los Angeles 162
Lawrence 113
Buffalo 108
Tokyo 106
Ho Chi Minh City 101
Munich 97
Zhengzhou 92
Lauterbourg 91
Milan 89
Hanoi 81
Dallas 80
Moscow 72
Chicago 70
San Diego 69
São Paulo 63
Menlo Park 51
Nuremberg 48
Phoenix 47
London 39
Orem 39
Montreal 37
Frankfurt am Main 36
Mülheim 35
Shanghai 35
Brooklyn 34
Engelhard 32
Atlanta 30
Brussels 28
Jakarta 27
Toronto 26
Chennai 25
Naples 25
Center 24
Hefei 24
Redondo Beach 24
Warsaw 24
Florence 23
Nanjing 23
North Bergen 23
Redwood City 23
Pune 22
Salt Lake City 22
Amsterdam 21
Dong Ket 21
Bologna 19
Manchester 19
San Mateo 19
Boardman 18
Falls Church 18
Mountain View 18
Poplar 18
Seoul 18
Da Nang 17
St. George 17
Vienna 17
Rio de Janeiro 16
Turin 16
Turku 16
University Park 16
Ankara 15
Chongqing 15
Denver 15
Elk Grove Village 15
Norwalk 15
Stockholm 15
Vancouver 14
Baghdad 13
Guangzhou 13
Monte Vista 13
Brno 12
Columbus 12
Del Norte 12
Johannesburg 12
San Francisco 12
Verona 12
Biên Hòa 11
Catania 11
Totale 35.628
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Nome #
Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome. 666
Fulminant Fusobacterium necrophorum meningitis in an immunocompetent adolescent 607
Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency 546
Chronic granulomatous disease: Clinical, molecular, and therapeutic aspects 536
Bruton's tyrosine kinase defect in dendritic cells from X-linked agammaglobulinaemia patients does not influence their differentiation, maturation and antigen-presenting cell function 515
A 2-month-old male with pyuria and persistent fever 515
Hereditary Deficiency of gp91(phox) Is Associated With Enhanced Arterial Dilatation Results of a Multicenter Study 513
Clinical features and follow-up in patients with 22q11.2 deletion syndrome 508
A 13-year-old girl with recurrent inguinal lymphadenopathy. 507
Chronic Granulomatous Disease Presenting with Salmonella Brain Abscesses. 506
Immunodeficiency in Vici Syndrome: a Heterogeneous Phenotype 493
Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: An Italian multicenter study 491
Dual-regulated lentiviral vector for gene therapy of X-linked chronic granulomatosis 491
Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy 491
Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: An Italian multicenter study 486
Rh system and intrauterine growth. Interaction with season of birth 483
Does NADPH oxidase deficiency cause artery dilatation in humans? 482
Inherited human gp91phox deficiency is associated with impaired isoprostane formation and platelet dysfunction 480
Intra-Erythrocyte Infusion of Dexamethasone Reduces Neurological Symptoms in Ataxia Teleangiectasia Patients: Results of a Phase 2 Trial. 477
Transitory hypogammaglobulinemia of infancy in FG syndrome [2] 474
Rapid T-cell receptor CD4+ repertoire reconstitution and immune recovery in unrelated umbilical cord blood transplanted pediatric leukemia patients 473
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 472
The impact of TACI mutations: from hypogammaglobulinemia in infancy to autoimmunity in adulthood 467
Lack of iNKT cells in patients with combined immune deficiency due to hypomorphic RAG mutations 465
Visceral leishmaniasis revealing chronic granulomatous diseases in a child 464
The Quality of Life of Children and Adolescents with X-Linked Agammaglobulinemia 461
Etiology, clinical outcome, and laboratory features in children with neutropenia: analysis of 104 cases 457
Role of reduced intensity conditioning in T-cell and B-cell immune reconstitution after HLA-identical bone marrow transplantation in ADA-SCID 453
Relapsing Campylobacter jejuni Systemic Infections in a Child with X-Linked Agammaglobulinemia 449
gp91phox-dependent expression of platelet CD40 ligand 448
Reduced Atherosclerotic Burden in Subjects With Genetically Determined Low Oxidative Stress 444
. Serum Soluble ST2 as Diagnostic Marker of Systemic Inflammatory Reactive Syndrome of Bacterial Etiology in Children. 444
Serum soluble ST2 as diagnostic marker of systemic inflammatory reactive syndrome of bacterial etiology in children. 440
Pancytopenia and severe sepsis in an adult case of congenital X-linked agammaglobulinemia (XLA) 434
Preclinical safety and efficacy of human CD34(+) cells transduced with lentiviral vector for the treatment of Wiskott-Aldrich syndrome 434
HLA-haploidentical stem cell transplantation after removal of αβ+ T and B cells in children with nonmalignant disorders 432
Effectiveness of immunoglobulin replacement therapy on clinical outcome in patients with primary antibody deficiencies: results from a multicenter prospective cohort study 427
Successful treatment with percutaneous transhepatic alcoholization of a liver abscess in a child with chronic granulomatous disease 426
“Maternal fetal interaction in the ABO system. A comparative analysis of healthy mothers and couples with R.S.A. suggests a protective effect of B incompatibility 424
Defective B-cell proliferation and maintenance of long-term memory in patients 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
X-chromosome inactivation and mutation pattern in the Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinemia. Italian XLA Collaborative Group 422
Evaluation of the relevance of humoral immunodeficiencies in a pediatric population affected by recurrent infections 418
Subcutaneous Immunoglobulin Replacement Therapy in Patients with Primary Immunodeficiency in Routine Clinical Practice: The VISPO Prospective Multicenter Study 418
Non invasive assessment of lung disease in ataxia telangiectasia by high-field magnetic resonance imaging 418
Shift from intravenous or 16% subcutaneous replacement therapy to 20% subcutaneous immunoglobulin in patients with primary antibody deficiencies 418
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia 416
Different degrees of NADPH oxidase 2 regulation and in vivo platelet activation: lesson from chronic granulomatous disease 409
How should eosinophilic cystitis be treated in patients with chronic granulomatous disease? 407
Humoral immune responses and CD27+B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome) 406
Post-natal ontogenesis of the T-cell receptor CD4 and CD8 V beta repertoire and immune function in children with DiGeorge syndrome 406
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 405
Clinical characterization of hypogammaglobulinemia. 398
Nox2 is determinant for ischemia-induced oxidative stress and arterial vasodilatation: a pilot study in patients with hereditary Nox2 deficiency 397
X-linked Lymphoproliferative Disease due to SAP/SH2D1A deficiency: A Multicentre Study on the manifestations, management and outcome of the disease 397
[Goiter prevalence and urinary excretion of iodine in a sample of school age children in the city of Rome] 396
Consanguinity and polygenic diseases: a model for antibody deficiencies 394
Immunodeficiency in Vici syndrome: a heterogeneous phenotype 391
Caratterizzazione clinica di pazienti con ipogammaglobulinemia. 388
Hyper Ige syndrome(HIES):description of patients with different clinical and molecular phenotype. 381
Caratterizzazione genetica di pazienti pediatrici con ipogammaglobulinemia. 374
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 371
Outcome of hematopoietic stem cell transplantation for adenosine deaminase-deficient severe combined immunodeficiency 371
Molecular characterization of TNFRSF13B gene in pediatric patients with hypogammaglobulinemia. 370
Familial Hemophagocytic Lymphohistiocytosis Type 3 Diagnosed at School Age: A Case Report 364
Evidence of clonotypic pattern of T-cell repertoire in synovial fluid of children with juvenile rheumatoid arthritis at the onset of the disease 362
Parvovirus(PV B19) infection and juvenile chronic arthritis 362
Dermatite non solo atopica: descrizione di due casi di sindrome da Iper IgE (HIES) 356
Late-onset combined immune-deficiency due to LIGIV mutations in a 12 years old patient 354
Cutaneous granulomatosis and combined immunodeficiency revealing Ataxia-Telangiectasia: a case report 353
Parvovirus (PV B19) infection and juvenile chronic arthritis 344
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 334
Evidence of clonotypic pattern of T cell repertoire in synovial fluid of children with juvenile rheumatoid arthritis at the onset of the disease. 326
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. 320
Immunoglobulin subclasses and specific antihemophilus influentiae response in children with recurrent infections 296
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 284
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 265
The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment 241
Idiopathic neutropenia of infancy: Data from the Italian Neutropenia Registry 237
First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia 237
Diagnosis and management of neutropenia in children: The approach of the Study Group on Neutropenia and Marrow Failure Syndromes of the Pediatric Italian Hemato-Oncology Association (Associazione Italiana Emato-Oncologia Pediatrica - AIEOP) 226
Phenotypical T Cell Differentiation Analysis: A Diagnostic and Predictive Tool in the Study of Primary Immunodeficiencies 225
Impaired X-CGD T cell compartment is gp91phox-NADPH oxidase independent 224
Autoimmune neutropenia of childhood secondary to other autoimmune disorders: Data from the Italian neutropenia registry 215
Characterization of T and B cell repertoire diversity in patients with RAG deficiency 214
Diagnostic Approach to Monogenic Inflammatory Bowel Disease in Clinical Practice: A Ten-Year Multicentric Experience 212
The Interplay between CD27dull and CD27bright B Cells Ensures the Flexibility, Stability, and Resilience of Human B Cell Memory 206
Urogenital Abnormalities in Adenosine Deaminase Deficiency 205
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) 204
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 200
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. 199
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function 197
PEDIATRIA 196
Immunotherapy with an HIV-DNA vaccine in children and adults 194
Evaluation of mother’s stress during hospitalization can influence the breastfeeding rate. Experience in intensive and non intensive departments 192
Health-Related Quality of Life and Emotional Difficulties in Chronic Granulomatous Disease: Data on Adult and Pediatric Patients from Italian Network for Primary Immunodeficiency (IPINet) 190
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection 188
Waning of vaccine-induced immunity to measles in kidney transplanted children 187
Fungal infections of the lung in children 187
Totale 38.100
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Categoria #
all - tutte 117.387
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 117.387
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.253 0 164 83 67 93 91 56 58 145 87 75 334
2022/20231.569 150 121 42 185 93 428 179 115 126 5 91 34
2023/2024821 79 74 35 33 65 183 80 58 26 9 43 136
2024/20253.807 123 851 387 215 162 263 302 163 332 326 421 262
2025/20266.505 535 316 618 550 594 306 803 733 774 523 493 260
2026/2027727 429 298 0 0 0 0 0 0 0 0 0 0
Totale 44.064