IRIS
FINOCCHI, ANDREA
 Distribuzione geografica
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Continente #
NA - Nord America 32.575
AS - Asia 4.675
EU - Europa 4.370
SA - Sud America 690
AF - Africa 57
OC - Oceania 23
Continente sconosciuto - Info sul continente non disponibili 4
Totale 42.394
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Nazione #
US - Stati Uniti d'America 32.431
SG - Singapore 2.228
CN - Cina 987
IT - Italia 876
DE - Germania 751
RU - Federazione Russa 596
BR - Brasile 565
HK - Hong Kong 458
UA - Ucraina 387
IE - Irlanda 384
VN - Vietnam 337
FI - Finlandia 316
FR - Francia 286
GB - Regno Unito 261
SE - Svezia 216
JP - Giappone 128
IN - India 102
KR - Corea 95
CA - Canada 81
NL - Olanda 73
BD - Bangladesh 56
AR - Argentina 54
ID - Indonesia 44
AT - Austria 43
PL - Polonia 42
TR - Turchia 41
MX - Messico 40
ES - Italia 39
IQ - Iraq 36
BE - Belgio 32
KG - Kirghizistan 24
AU - Australia 22
EC - Ecuador 22
ZA - Sudafrica 20
CO - Colombia 16
CZ - Repubblica Ceca 16
IR - Iran 15
PH - Filippine 14
SA - Arabia Saudita 14
PK - Pakistan 13
UZ - Uzbekistan 12
JO - Giordania 10
CL - Cile 9
KE - Kenya 9
MY - Malesia 8
PE - Perù 8
VE - Venezuela 8
EG - Egitto 7
IL - Israele 7
PT - Portogallo 7
AE - Emirati Arabi Uniti 6
CH - Svizzera 6
LT - Lituania 6
MA - Marocco 6
TH - Thailandia 6
AZ - Azerbaigian 5
BG - Bulgaria 5
DO - Repubblica Dominicana 4
DZ - Algeria 4
LB - Libano 4
NG - Nigeria 4
NP - Nepal 4
PY - Paraguay 4
RS - Serbia 4
CR - Costa Rica 3
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
TW - Taiwan 3
AL - Albania 2
BY - Bielorussia 2
DM - Dominica 2
GD - Grenada 2
HN - Honduras 2
HU - Ungheria 2
LV - Lettonia 2
OM - Oman 2
PS - Palestinian Territory 2
SV - El Salvador 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
GH - Ghana 1
GT - Guatemala 1
GY - Guiana 1
Totale 42.387
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Città #
Woodbridge 8.272
Wilmington 7.995
Houston 7.328
Singapore 1.247
Fairfield 1.088
Ashburn 824
Ann Arbor 675
San Jose 581
Chandler 525
Seattle 503
Hong Kong 448
Beijing 396
Cambridge 374
Dublin 357
Jacksonville 345
Medford 250
Rome 231
Helsinki 215
Santa Clara 199
The Dalles 189
Dearborn 185
Council Bluffs 148
New York 148
Los Angeles 138
Lawrence 114
Tokyo 105
Ho Chi Minh City 102
Munich 97
Buffalo 95
Lauterbourg 93
Zhengzhou 92
Hanoi 77
Milan 73
Moscow 72
Dallas 66
San Diego 65
São Paulo 65
Chicago 59
Menlo Park 51
Nuremberg 49
London 39
Orem 37
Frankfurt am Main 36
Mülheim 35
Shanghai 34
Engelhard 32
Montreal 29
Brussels 28
Jakarta 28
Phoenix 27
Brooklyn 26
Chennai 25
Redondo Beach 25
Warsaw 25
Center 24
Hefei 24
Atlanta 23
Nanjing 23
Redwood City 23
Pune 22
Amsterdam 21
Dong Ket 21
North Bergen 21
Salt Lake City 20
Toronto 20
Boardman 19
Manchester 19
Poplar 19
San Mateo 19
Bologna 18
Falls Church 18
Florence 18
Mountain View 18
Seoul 18
St. George 17
Vienna 17
Da Nang 16
Denver 16
Rio de Janeiro 16
Turku 16
University Park 16
Ankara 15
Chongqing 15
Elk Grove Village 15
Norwalk 15
Stockholm 15
Baghdad 13
Guangzhou 13
Naples 13
Turin 13
Vancouver 13
Brno 12
Del Norte 12
Johannesburg 12
Verona 12
Biên Hòa 11
Haiphong 11
Mumbai 11
San Francisco 11
Amman 10
Totale 35.126
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Nome #
Fulminant Fusobacterium necrophorum meningitis in an immunocompetent adolescent 594
Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome. 563
Chronic granulomatous disease: Clinical, molecular, and therapeutic aspects 530
Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency 529
A 2-month-old male with pyuria and persistent fever 509
Bruton's tyrosine kinase defect in dendritic cells from X-linked agammaglobulinaemia patients does not influence their differentiation, maturation and antigen-presenting cell function 508
Hereditary Deficiency of gp91(phox) Is Associated With Enhanced Arterial Dilatation Results of a Multicenter Study 506
A 13-year-old girl with recurrent inguinal lymphadenopathy. 500
Clinical features and follow-up in patients with 22q11.2 deletion syndrome 498
Chronic Granulomatous Disease Presenting with Salmonella Brain Abscesses. 496
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 487
Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: An Italian multicenter study 483
Rh system and intrauterine growth. Interaction with season of birth 480
Dual-regulated lentiviral vector for gene therapy of X-linked chronic granulomatosis 477
Does NADPH oxidase deficiency cause artery dilatation in humans? 477
Transitory hypogammaglobulinemia of infancy in FG syndrome [2] 473
Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: An Italian multicenter study 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 467
Inherited human gp91phox deficiency is associated with impaired isoprostane formation and platelet dysfunction 465
Rapid T-cell receptor CD4+ repertoire reconstitution and immune recovery in unrelated umbilical cord blood transplanted pediatric leukemia patients 463
Visceral leishmaniasis revealing chronic granulomatous diseases in a child 462
The impact of TACI mutations: from hypogammaglobulinemia in infancy to autoimmunity in adulthood 461
Intra-Erythrocyte Infusion of Dexamethasone Reduces Neurological Symptoms in Ataxia Teleangiectasia Patients: Results of a Phase 2 Trial. 460
Lack of iNKT cells in patients with combined immune deficiency due to hypomorphic RAG mutations 459
The Quality of Life of Children and Adolescents with X-Linked Agammaglobulinemia 456
Etiology, clinical outcome, and laboratory features in children with neutropenia: analysis of 104 cases 452
Role of reduced intensity conditioning in T-cell and B-cell immune reconstitution after HLA-identical bone marrow transplantation in ADA-SCID 448
Relapsing Campylobacter jejuni Systemic Infections in a Child with X-Linked Agammaglobulinemia 447
gp91phox-dependent expression of platelet CD40 ligand 445
Reduced Atherosclerotic Burden in Subjects With Genetically Determined Low Oxidative Stress 443
. Serum Soluble ST2 as Diagnostic Marker of Systemic Inflammatory Reactive Syndrome of Bacterial Etiology in Children. 440
Serum soluble ST2 as diagnostic marker of systemic inflammatory reactive syndrome of bacterial etiology in children. 437
Preclinical safety and efficacy of human CD34(+) cells transduced with lentiviral vector for the treatment of Wiskott-Aldrich syndrome 429
Pancytopenia and severe sepsis in an adult case of congenital X-linked agammaglobulinemia (XLA) 426
Successful treatment with percutaneous transhepatic alcoholization of a liver abscess in a child with chronic granulomatous disease 423
Effectiveness of immunoglobulin replacement therapy on clinical outcome in patients with primary antibody deficiencies: results from a multicenter prospective cohort study 421
The impact of TACI mutations in children affected with hypogammaglobulinemia and in their relatives with autoimmunity: a matter of age. 420
X-chromosome inactivation and mutation pattern in the Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinemia. Italian XLA Collaborative Group 419
“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 418
Defective B-cell proliferation and maintenance of long-term memory in patients with chronic granulomatous disease 417
Evaluation of the relevance of humoral immunodeficiencies in a pediatric population affected by recurrent infections 413
Shift from intravenous or 16% subcutaneous replacement therapy to 20% subcutaneous immunoglobulin in patients with primary antibody deficiencies 413
HLA-haploidentical stem cell transplantation after removal of αβ+ T and B cells in children with nonmalignant disorders 410
Subcutaneous Immunoglobulin Replacement Therapy in Patients with Primary Immunodeficiency in Routine Clinical Practice: The VISPO Prospective Multicenter Study 409
Non invasive assessment of lung disease in ataxia telangiectasia by high-field magnetic resonance imaging 409
Post-natal ontogenesis of the T-cell receptor CD4 and CD8 V beta repertoire and immune function in children with DiGeorge syndrome 404
Different degrees of NADPH oxidase 2 regulation and in vivo platelet activation: lesson from chronic granulomatous disease 404
Serratia marcescens Osteomyelitis in a Newborn with Chronic Granulomatous 404
Humoral immune responses and CD27+B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome) 403
Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience 403
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia 402
How should eosinophilic cystitis be treated in patients with chronic granulomatous disease? 400
Nox2 is determinant for ischemia-induced oxidative stress and arterial vasodilatation: a pilot study in patients with hereditary Nox2 deficiency 395
X-linked Lymphoproliferative Disease due to SAP/SH2D1A deficiency: A Multicentre Study on the manifestations, management and outcome of the disease 394
[Goiter prevalence and urinary excretion of iodine in a sample of school age children in the city of Rome] 392
Consanguinity and polygenic diseases: a model for antibody deficiencies 388
Clinical characterization of hypogammaglobulinemia. 383
Caratterizzazione clinica di pazienti con ipogammaglobulinemia. 382
Immunodeficiency in Vici syndrome: a heterogeneous phenotype 380
Hyper Ige syndrome(HIES):description of patients with different clinical and molecular phenotype. 376
Caratterizzazione genetica di pazienti pediatrici con ipogammaglobulinemia. 374
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 368
Molecular characterization of TNFRSF13B gene in pediatric patients with hypogammaglobulinemia. 368
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 357
Evidence of clonotypic pattern of T-cell repertoire in synovial fluid of children with juvenile rheumatoid arthritis at the onset of the disease 356
Dermatite non solo atopica: descrizione di due casi di sindrome da Iper IgE (HIES) 353
Late-onset combined immune-deficiency due to LIGIV mutations in a 12 years old patient 351
Cutaneous granulomatosis and combined immunodeficiency revealing Ataxia-Telangiectasia: a case report 350
Parvovirus (PV B19) infection and juvenile chronic arthritis 341
Evidence of clonotypic pattern of T cell repertoire in synovial fluid of children with juvenile rheumatoid arthritis at the onset of the disease. 323
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 320
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. 314
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 280
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 246
First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia 232
The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment 226
Phenotypical T Cell Differentiation Analysis: A Diagnostic and Predictive Tool in the Study of Primary Immunodeficiencies 215
Impaired X-CGD T cell compartment is gp91phox-NADPH oxidase independent 214
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 210
Idiopathic neutropenia of infancy: Data from the Italian Neutropenia Registry 210
Autoimmune neutropenia of childhood secondary to other autoimmune disorders: Data from the Italian neutropenia registry 209
Urogenital Abnormalities in Adenosine Deaminase Deficiency 198
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) 195
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) 194
The Interplay between CD27dull and CD27bright B Cells Ensures the Flexibility, Stability, and Resilience of Human B Cell Memory 193
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 192
PEDIATRIA 191
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. 191
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function 188
Evaluation of mother’s stress during hospitalization can influence the breastfeeding rate. Experience in intensive and non intensive departments 184
Immunotherapy with an HIV-DNA vaccine in children and adults 183
Waning of vaccine-induced immunity to measles in kidney transplanted children 182
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) 182
Fungal infections of the lung in children 182
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection 180
Totale 37.297
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Categoria #
all - tutte 109.563
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 109.563
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021317 0 0 0 0 0 0 0 0 0 0 213 104
2021/20221.322 56 164 83 67 93 95 57 58 150 87 75 337
2022/20231.588 152 123 42 186 94 434 182 115 128 5 91 36
2023/2024826 80 74 36 34 65 183 80 58 27 10 43 136
2024/20253.882 125 880 400 218 162 270 305 163 335 335 425 264
2025/20265.905 539 320 625 561 605 309 810 742 788 529 77 0
Totale 42.849