IRIS
FINOCCHI, ANDREA
 Distribuzione geografica
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Continente #
NA - Nord America 33.018
AS - Asia 4.758
EU - Europa 4.460
SA - Sud America 685
AF - Africa 57
OC - Oceania 23
Continente sconosciuto - Info sul continente non disponibili 4
Totale 43.005
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Nazione #
US - Stati Uniti d'America 32.848
SG - Singapore 2.194
CN - Cina 993
IT - Italia 982
DE - Germania 752
RU - Federazione Russa 590
BR - Brasile 559
HK - Hong Kong 449
UA - Ucraina 387
IE - Irlanda 378
VN - Vietnam 341
FI - Finlandia 312
FR - Francia 283
GB - Regno Unito 260
SE - Svezia 216
BD - Bangladesh 165
JP - Giappone 129
IN - India 103
CA - Canada 97
KR - Corea 95
NL - Olanda 73
AR - Argentina 54
ID - Indonesia 44
AT - Austria 43
MX - Messico 42
TR - Turchia 42
PL - Polonia 41
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
PH - Filippine 14
PK - Pakistan 14
SA - Arabia Saudita 14
UZ - Uzbekistan 12
CL - Cile 10
JO - Giordania 10
MY - Malesia 10
KE - Kenya 9
VE - Venezuela 8
EG - Egitto 7
IL - Israele 7
PE - Perù 7
PT - Portogallo 7
AE - Emirati Arabi Uniti 6
CH - Svizzera 6
LT - Lituania 6
MA - Marocco 6
TH - Thailandia 6
AZ - Azerbaigian 5
PY - Paraguay 5
BG - Bulgaria 4
CR - Costa Rica 4
DZ - Algeria 4
JM - Giamaica 4
LB - Libano 4
NG - Nigeria 4
NP - Nepal 4
RS - Serbia 4
TW - Taiwan 4
DK - Danimarca 3
EE - Estonia 3
EU - Europa 3
GR - Grecia 3
GT - Guatemala 3
KZ - Kazakistan 3
MD - Moldavia 3
PA - Panama 3
QA - Qatar 3
RO - Romania 3
SV - El Salvador 3
SY - Repubblica araba siriana 3
TN - Tunisia 3
AL - Albania 2
BY - Bielorussia 2
DM - Dominica 2
DO - Repubblica Dominicana 2
GD - Grenada 2
HN - Honduras 2
HU - Ungheria 2
LV - Lettonia 2
OM - Oman 2
PS - Palestinian Territory 2
TT - Trinidad e Tobago 2
UY - Uruguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AO - Angola 1
AW - Aruba 1
BH - Bahrain 1
BO - Bolivia 1
BZ - Belize 1
CY - Cipro 1
GA - Gabon 1
GE - Georgia 1
Totale 42.994
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Città #
Woodbridge 8.272
Wilmington 7.995
Houston 7.330
Singapore 1.220
Fairfield 1.085
Ashburn 874
Ann Arbor 675
San Jose 624
Chandler 519
Seattle 505
Hong Kong 438
Beijing 393
Cambridge 389
Dublin 351
Jacksonville 346
Medford 248
Rome 248
Council Bluffs 214
Santa Clara 212
Helsinki 211
The Dalles 188
Dearborn 185
New York 173
Los Angeles 147
Lawrence 112
Buffalo 106
Tokyo 106
Ho Chi Minh City 101
Munich 97
Zhengzhou 92
Lauterbourg 91
Milan 85
Hanoi 81
Dallas 76
Moscow 72
San Diego 69
Chicago 68
São Paulo 63
Menlo Park 51
Nuremberg 48
London 39
Phoenix 38
Orem 37
Frankfurt am Main 36
Mülheim 35
Shanghai 34
Montreal 33
Engelhard 32
Brooklyn 28
Brussels 28
Jakarta 27
Toronto 26
Atlanta 25
Chennai 25
Center 24
Hefei 24
Redondo Beach 24
Warsaw 24
Nanjing 23
Redwood City 23
Pune 22
Amsterdam 21
Dong Ket 21
Naples 21
North Bergen 20
Salt Lake City 20
Bologna 19
Manchester 19
San Mateo 19
Boardman 18
Falls Church 18
Florence 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 35.387
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Nome #
Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome. 638
Fulminant Fusobacterium necrophorum meningitis in an immunocompetent adolescent 601
Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency 536
Chronic granulomatous disease: Clinical, molecular, and therapeutic aspects 531
Bruton's tyrosine kinase defect in dendritic cells from X-linked agammaglobulinaemia patients does not influence their differentiation, maturation and antigen-presenting cell function 513
Hereditary Deficiency of gp91(phox) Is Associated With Enhanced Arterial Dilatation Results of a Multicenter Study 513
A 2-month-old male with pyuria and persistent fever 511
A 13-year-old girl with recurrent inguinal lymphadenopathy. 504
Clinical features and follow-up in patients with 22q11.2 deletion syndrome 503
Chronic Granulomatous Disease Presenting with Salmonella Brain Abscesses. 502
Immunodeficiency in Vici Syndrome: a Heterogeneous Phenotype 489
Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy 489
Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: An Italian multicenter study 488
Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: An Italian multicenter study 486
Dual-regulated lentiviral vector for gene therapy of X-linked chronic granulomatosis 485
Does NADPH oxidase deficiency cause artery dilatation in humans? 482
Rh system and intrauterine growth. Interaction with season of birth 481
Inherited human gp91phox deficiency is associated with impaired isoprostane formation and platelet dysfunction 480
Transitory hypogammaglobulinemia of infancy in FG syndrome [2] 474
Intra-Erythrocyte Infusion of Dexamethasone Reduces Neurological Symptoms in Ataxia Teleangiectasia Patients: Results of a Phase 2 Trial. 472
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 469
Rapid T-cell receptor CD4+ repertoire reconstitution and immune recovery in unrelated umbilical cord blood transplanted pediatric leukemia patients 466
Lack of iNKT cells in patients with combined immune deficiency due to hypomorphic RAG mutations 464
The impact of TACI mutations: from hypogammaglobulinemia in infancy to autoimmunity in adulthood 464
Visceral leishmaniasis revealing chronic granulomatous diseases in a child 462
The Quality of Life of Children and Adolescents with X-Linked Agammaglobulinemia 459
Etiology, clinical outcome, and laboratory features in children with neutropenia: analysis of 104 cases 456
Role of reduced intensity conditioning in T-cell and B-cell immune reconstitution after HLA-identical bone marrow transplantation in ADA-SCID 450
gp91phox-dependent expression of platelet CD40 ligand 448
Relapsing Campylobacter jejuni Systemic Infections in a Child with X-Linked Agammaglobulinemia 447
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. 442
Serum soluble ST2 as diagnostic marker of systemic inflammatory reactive syndrome of bacterial etiology in children. 439
Preclinical safety and efficacy of human CD34(+) cells transduced with lentiviral vector for the treatment of Wiskott-Aldrich syndrome 434
Pancytopenia and severe sepsis in an adult case of congenital X-linked agammaglobulinemia (XLA) 431
Successful treatment with percutaneous transhepatic alcoholization of a liver abscess in a child 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
Effectiveness of immunoglobulin replacement therapy on clinical outcome in patients with primary antibody deficiencies: results from a multicenter prospective cohort study 423
Defective B-cell proliferation and maintenance of long-term memory in patients with chronic granulomatous disease 422
X-chromosome inactivation and mutation pattern in the Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinemia. Italian XLA Collaborative Group 422
“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 421
HLA-haploidentical stem cell transplantation after removal of αβ+ T and B cells in children with nonmalignant disorders 420
Shift from intravenous or 16% subcutaneous replacement therapy to 20% subcutaneous immunoglobulin in patients with primary antibody deficiencies 418
Non invasive assessment of lung disease in ataxia telangiectasia by high-field magnetic resonance imaging 416
Evaluation of the relevance of humoral immunodeficiencies in a pediatric population affected by recurrent infections 415
Subcutaneous Immunoglobulin Replacement Therapy in Patients with Primary Immunodeficiency in Routine Clinical Practice: The VISPO Prospective Multicenter Study 414
Different degrees of NADPH oxidase 2 regulation and in vivo platelet activation: lesson from chronic granulomatous disease 409
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
How should eosinophilic cystitis be treated in patients with chronic granulomatous disease? 406
Serratia marcescens Osteomyelitis in a Newborn with Chronic Granulomatous 406
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia 404
Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience 404
Nox2 is determinant for ischemia-induced oxidative stress and arterial vasodilatation: a pilot study in patients with hereditary Nox2 deficiency 396
X-linked Lymphoproliferative Disease due to SAP/SH2D1A deficiency: A Multicentre Study on the manifestations, management and outcome of the disease 396
Consanguinity and polygenic diseases: a model for antibody deficiencies 394
Clinical characterization of hypogammaglobulinemia. 394
[Goiter prevalence and urinary excretion of iodine in a sample of school age children in the city of Rome] 393
Immunodeficiency in Vici syndrome: a heterogeneous phenotype 389
Caratterizzazione clinica di pazienti con ipogammaglobulinemia. 385
Hyper Ige syndrome(HIES):description of patients with different clinical and molecular phenotype. 377
Caratterizzazione genetica di pazienti pediatrici con ipogammaglobulinemia. 374
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 369
Molecular characterization of TNFRSF13B gene in pediatric patients with hypogammaglobulinemia. 369
Outcome of hematopoietic stem cell transplantation for adenosine deaminase-deficient severe combined immunodeficiency 366
Familial Hemophagocytic Lymphohistiocytosis Type 3 Diagnosed at School Age: A Case Report 363
Parvovirus(PV B19) infection and juvenile chronic arthritis 359
Evidence of clonotypic pattern of T-cell repertoire in synovial fluid of children with juvenile rheumatoid arthritis at the onset of the disease 357
Dermatite non solo atopica: descrizione di due casi di sindrome da Iper IgE (HIES) 354
Late-onset combined immune-deficiency due to LIGIV mutations in a 12 years old patient 353
Cutaneous granulomatosis and combined immunodeficiency revealing Ataxia-Telangiectasia: a case report 351
Parvovirus (PV B19) infection and juvenile chronic arthritis 341
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 326
Evidence of clonotypic pattern of T cell repertoire in synovial fluid of children with juvenile rheumatoid arthritis at the onset of the disease. 324
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. 318
Immunoglobulin subclasses and specific antihemophilus influentiae response in children with recurrent infections 291
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 281
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 257
The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment 235
First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia 234
Idiopathic neutropenia of infancy: Data from the Italian Neutropenia Registry 232
Impaired X-CGD T cell compartment is gp91phox-NADPH oxidase independent 219
Phenotypical T Cell Differentiation Analysis: A Diagnostic and Predictive Tool in the Study of Primary Immunodeficiencies 218
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) 217
Characterization of T and B cell repertoire diversity in patients with RAG deficiency 212
Diagnostic Approach to Monogenic Inflammatory Bowel Disease in Clinical Practice: A Ten-Year Multicentric Experience 211
Autoimmune neutropenia of childhood secondary to other autoimmune disorders: Data from the Italian neutropenia registry 209
Urogenital Abnormalities in Adenosine Deaminase Deficiency 202
The Interplay between CD27dull and CD27bright B Cells Ensures the Flexibility, Stability, and Resilience of Human B Cell Memory 201
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 197
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) 196
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. 195
PEDIATRIA 192
Evaluation of mother’s stress during hospitalization can influence the breastfeeding rate. Experience in intensive and non intensive departments 191
Immunotherapy with an HIV-DNA vaccine in children and adults 190
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function 189
Waning of vaccine-induced immunity to measles in kidney transplanted children 185
Fungal infections of the lung in children 185
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection 184
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) 183
Totale 37.765
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Categoria #
all - tutte 113.920
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 113.920
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.309 56 164 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
2026/2027154 154 0 0 0 0 0 0 0 0 0 0 0
Totale 43.491