IRIS
FINOCCHI, ANDREA
 Distribuzione geografica
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Continente #
NA - Nord America 34.862
AS - Asia 4.837
EU - Europa 4.641
SA - Sud America 716
Continente sconosciuto - Info sul continente non disponibili 491
AF - Africa 60
OC - Oceania 23
Totale 45.630
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Nazione #
US - Stati Uniti d'America 34.588
SG - Singapore 2.204
IT - Italia 1.083
CN - Cina 1.003
DE - Germania 753
RU - Federazione Russa 590
BR - Brasile 572
HK - Hong Kong 453
UA - Ucraina 387
IE - Irlanda 379
VN - Vietnam 344
FI - Finlandia 312
FR - Francia 284
SE - Svezia 275
GB - Regno Unito 269
BD - Bangladesh 198
CA - Canada 138
JP - Giappone 130
IN - India 105
KR - Corea 95
NL - Olanda 77
AR - Argentina 55
ID - Indonesia 47
MX - Messico 47
AT - Austria 43
TR - Turchia 43
PL - Polonia 42
ES - Italia 39
IQ - Iraq 36
BE - Belgio 32
EC - Ecuador 29
KG - Kirghizistan 25
CO - Colombia 24
AU - Australia 22
CZ - Repubblica Ceca 20
ZA - Sudafrica 20
SA - Arabia Saudita 19
CR - Costa Rica 16
IR - Iran 15
PH - Filippine 15
PK - Pakistan 14
JM - Giamaica 13
UZ - Uzbekistan 12
MY - Malesia 11
TT - Trinidad e Tobago 11
CL - Cile 10
JO - Giordania 10
VE - Venezuela 10
KE - Kenya 9
GT - Guatemala 8
SV - El Salvador 8
EG - Egitto 7
HN - Honduras 7
IL - Israele 7
PE - Perù 7
PT - Portogallo 7
TH - Thailandia 7
AE - Emirati Arabi Uniti 6
CH - Svizzera 6
LT - Lituania 6
MA - Marocco 6
NG - Nigeria 6
AZ - Azerbaigian 5
BG - Bulgaria 5
EE - Estonia 5
LB - Libano 5
NI - Nicaragua 5
PY - Paraguay 5
TW - Taiwan 5
DZ - Algeria 4
NP - Nepal 4
RS - Serbia 4
BZ - Belize 3
DK - Danimarca 3
EU - Europa 3
GD - Grenada 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
BH - Bahrain 2
BY - Bielorussia 2
DM - Dominica 2
DO - Repubblica Dominicana 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
Totale 45.128
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Città #
Woodbridge 8.272
Wilmington 7.995
Houston 7.332
Singapore 1.224
Fairfield 1.085
Ashburn 1.064
San Jose 790
Ann Arbor 675
Chandler 519
Seattle 511
Hong Kong 442
Beijing 400
Cambridge 395
Dublin 351
Jacksonville 348
Council Bluffs 314
Rome 259
Medford 248
Santa Clara 224
Helsinki 211
New York 191
The Dalles 188
Dearborn 186
Los Angeles 170
Lawrence 113
Buffalo 112
Tokyo 107
Ho Chi Minh City 101
Munich 97
Milan 92
Zhengzhou 92
Lauterbourg 91
Dallas 83
Hanoi 82
Chicago 76
Phoenix 76
Moscow 72
San Diego 70
São Paulo 64
Denver 55
Menlo Park 51
Nuremberg 48
Columbus 41
London 39
Orem 39
Brooklyn 38
Atlanta 37
Frankfurt am Main 37
Montreal 37
Mülheim 35
Shanghai 35
Toronto 33
Engelhard 32
Brussels 28
Jakarta 27
Naples 27
Chennai 25
Salt Lake City 25
Center 24
Hefei 24
Redondo Beach 24
Warsaw 24
Florence 23
Nanjing 23
North Bergen 23
Redwood City 23
Boardman 22
Bologna 22
Pune 22
Amsterdam 21
Dong Ket 21
Manchester 19
San Francisco 19
San Mateo 19
Falls Church 18
Mountain View 18
Poplar 18
Seoul 18
Turin 18
Da Nang 17
St. George 17
Vienna 17
Elk Grove Village 16
Rio de Janeiro 16
Turku 16
University Park 16
Ankara 15
Chongqing 15
Norwalk 15
Stockholm 15
Vancouver 14
Washington 14
Baghdad 13
Guangzhou 13
Miami 13
Monte Vista 13
Brno 12
Del Norte 12
Johannesburg 12
San José 12
Totale 36.157
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Nome #
Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome. 702
Fulminant Fusobacterium necrophorum meningitis in an immunocompetent adolescent 622
Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency 555
Chronic granulomatous disease: Clinical, molecular, and therapeutic aspects 546
Hereditary Deficiency of gp91(phox) Is Associated With Enhanced Arterial Dilatation Results of a Multicenter Study 529
A 2-month-old male with pyuria and persistent fever 529
Bruton's tyrosine kinase defect in dendritic cells from X-linked agammaglobulinaemia patients does not influence their differentiation, maturation and antigen-presenting cell function 523
A 13-year-old girl with recurrent inguinal lymphadenopathy. 522
Clinical features and follow-up in patients with 22q11.2 deletion syndrome 518
Chronic Granulomatous Disease Presenting with Salmonella Brain Abscesses. 513
Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: An Italian multicenter study 506
Dual-regulated lentiviral vector for gene therapy of X-linked chronic granulomatosis 500
Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy 500
Immunodeficiency in Vici Syndrome: a Heterogeneous Phenotype 499
Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: An Italian multicenter study 498
Does NADPH oxidase deficiency cause artery dilatation in humans? 498
Inherited human gp91phox deficiency is associated with impaired isoprostane formation and platelet dysfunction 495
Rh system and intrauterine growth. Interaction with season of birth 491
Intra-Erythrocyte Infusion of Dexamethasone Reduces Neurological Symptoms in Ataxia Teleangiectasia Patients: Results of a Phase 2 Trial. 485
Rapid T-cell receptor CD4+ repertoire reconstitution and immune recovery in unrelated umbilical cord blood transplanted pediatric leukemia patients 482
Transitory hypogammaglobulinemia of infancy in FG syndrome [2] 479
Visceral leishmaniasis revealing chronic granulomatous diseases in a child 477
The impact of TACI mutations: from hypogammaglobulinemia in infancy to autoimmunity in adulthood 477
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 477
HLA-haploidentical stem cell transplantation after removal of αβ+ T and B cells in children with nonmalignant disorders 474
Lack of iNKT cells in patients with combined immune deficiency due to hypomorphic RAG mutations 472
Etiology, clinical outcome, and laboratory features in children with neutropenia: analysis of 104 cases 471
The Quality of Life of Children and Adolescents with X-Linked Agammaglobulinemia 468
Role of reduced intensity conditioning in T-cell and B-cell immune reconstitution after HLA-identical bone marrow transplantation in ADA-SCID 460
gp91phox-dependent expression of platelet CD40 ligand 457
. Serum Soluble ST2 as Diagnostic Marker of Systemic Inflammatory Reactive Syndrome of Bacterial Etiology in Children. 457
Relapsing Campylobacter jejuni Systemic Infections in a Child with X-Linked Agammaglobulinemia 456
Reduced Atherosclerotic Burden in Subjects With Genetically Determined Low Oxidative Stress 451
Preclinical safety and efficacy of human CD34(+) cells transduced with lentiviral vector for the treatment of Wiskott-Aldrich syndrome 449
Serum soluble ST2 as diagnostic marker of systemic inflammatory reactive syndrome of bacterial etiology in children. 447
Pancytopenia and severe sepsis in an adult case of congenital X-linked agammaglobulinemia (XLA) 443
The impact of TACI mutations in children affected with hypogammaglobulinemia and in their relatives with autoimmunity: a matter of age. 438
Successful treatment with percutaneous transhepatic alcoholization of a liver abscess in a child with chronic granulomatous disease 435
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia 434
Effectiveness of immunoglobulin replacement therapy on clinical outcome in patients with primary antibody deficiencies: results from a multicenter prospective cohort study 434
Defective B-cell proliferation and maintenance of long-term memory in patients with chronic granulomatous disease 433
“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 432
Non invasive assessment of lung disease in ataxia telangiectasia by high-field magnetic resonance imaging 431
X-chromosome inactivation and mutation pattern in the Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinemia. Italian XLA Collaborative Group 429
Evaluation of the relevance of humoral immunodeficiencies in a pediatric population affected by recurrent infections 427
Shift from intravenous or 16% subcutaneous replacement therapy to 20% subcutaneous immunoglobulin in patients with primary antibody deficiencies 426
Subcutaneous Immunoglobulin Replacement Therapy in Patients with Primary Immunodeficiency in Routine Clinical Practice: The VISPO Prospective Multicenter Study 424
Humoral immune responses and CD27+B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome) 419
Post-natal ontogenesis of the T-cell receptor CD4 and CD8 V beta repertoire and immune function in children with DiGeorge syndrome 419
Different degrees of NADPH oxidase 2 regulation and in vivo platelet activation: lesson from chronic granulomatous disease 417
How should eosinophilic cystitis be treated in patients with chronic granulomatous disease? 416
Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience 410
Serratia marcescens Osteomyelitis in a Newborn with Chronic Granulomatous 409
Consanguinity and polygenic diseases: a model for antibody deficiencies 406
X-linked Lymphoproliferative Disease due to SAP/SH2D1A deficiency: A Multicentre Study on the manifestations, management and outcome of the disease 406
[Goiter prevalence and urinary excretion of iodine in a sample of school age children in the city of Rome] 405
Caratterizzazione clinica di pazienti con ipogammaglobulinemia. 403
Immunodeficiency in Vici syndrome: a heterogeneous phenotype 402
Nox2 is determinant for ischemia-induced oxidative stress and arterial vasodilatation: a pilot study in patients with hereditary Nox2 deficiency 402
Clinical characterization of hypogammaglobulinemia. 402
Caratterizzazione genetica di pazienti pediatrici con ipogammaglobulinemia. 393
Hyper Ige syndrome(HIES):description of patients with different clinical and molecular phenotype. 384
Molecular characterization of TNFRSF13B gene in pediatric patients with hypogammaglobulinemia. 382
Outcome of hematopoietic stem cell transplantation for adenosine deaminase-deficient severe combined immunodeficiency 381
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 378
Familial Hemophagocytic Lymphohistiocytosis Type 3 Diagnosed at School Age: A Case Report 374
Parvovirus(PV B19) infection and juvenile chronic arthritis 368
Evidence of clonotypic pattern of T-cell repertoire in synovial fluid of children with juvenile rheumatoid arthritis at the onset of the disease 366
Late-onset combined immune-deficiency due to LIGIV mutations in a 12 years old patient 364
Dermatite non solo atopica: descrizione di due casi di sindrome da Iper IgE (HIES) 362
Cutaneous granulomatosis and combined immunodeficiency revealing Ataxia-Telangiectasia: a case report 360
Parvovirus (PV B19) infection and juvenile chronic arthritis 354
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 343
Evidence of clonotypic pattern of T cell repertoire in synovial fluid of children with juvenile rheumatoid arthritis at the onset of the disease. 327
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. 325
Immunoglobulin subclasses and specific antihemophilus influentiae response in children with recurrent infections 307
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 292
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 272
First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia 247
Idiopathic neutropenia of infancy: Data from the Italian Neutropenia Registry 246
The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment 245
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) 239
Impaired X-CGD T cell compartment is gp91phox-NADPH oxidase independent 233
Phenotypical T Cell Differentiation Analysis: A Diagnostic and Predictive Tool in the Study of Primary Immunodeficiencies 229
Diagnostic Approach to Monogenic Inflammatory Bowel Disease in Clinical Practice: A Ten-Year Multicentric Experience 223
Autoimmune neutropenia of childhood secondary to other autoimmune disorders: Data from the Italian neutropenia registry 223
Characterization of T and B cell repertoire diversity in patients with RAG deficiency 223
The Interplay between CD27dull and CD27bright B Cells Ensures the Flexibility, Stability, and Resilience of Human B Cell Memory 218
Urogenital Abnormalities in Adenosine Deaminase Deficiency 217
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) 213
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 206
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function 204
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. 204
PEDIATRIA 202
Evaluation of mother’s stress during hospitalization can influence the breastfeeding rate. Experience in intensive and non intensive departments 202
Immunotherapy with an HIV-DNA vaccine in children and adults 201
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) 199
Fungal infections of the lung in children 196
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection 195
Waning of vaccine-induced immunity to measles in kidney transplanted children 192
Totale 39.076
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Categoria #
all - tutte 122.088
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 122.088
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.006 0 0 0 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
2026/20272.293 429 377 1.159 328 0 0 0 0 0 0 0 0
Totale 45.630