IRIS
FINOCCHI, ANDREA
 Distribuzione geografica
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Continente #
NA - Nord America 31.786
AS - Asia 3.798
EU - Europa 3.532
SA - Sud America 653
AF - Africa 43
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 4
Totale 39.822
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Nazione #
US - Stati Uniti d'America 31.686
SG - Singapore 1.935
CN - Cina 808
IT - Italia 763
DE - Germania 738
BR - Brasile 544
HK - Hong Kong 435
UA - Ucraina 389
IE - Irlanda 381
RU - Federazione Russa 295
GB - Regno Unito 231
SE - Svezia 212
VN - Vietnam 157
FR - Francia 156
FI - Finlandia 117
KR - Corea 96
IN - India 80
NL - Olanda 57
CA - Canada 52
AR - Argentina 50
ID - Indonesia 44
AT - Austria 43
JP - Giappone 43
BD - Bangladesh 36
MX - Messico 36
ES - Italia 35
PL - Polonia 35
TR - Turchia 31
BE - Belgio 30
KG - Kirghizistan 24
EC - Ecuador 20
ZA - Sudafrica 19
IQ - Iraq 18
CZ - Repubblica Ceca 14
IR - Iran 13
CO - Colombia 12
PK - Pakistan 10
CL - Cile 8
PE - Perù 8
PH - Filippine 8
PT - Portogallo 7
SA - Arabia Saudita 7
UZ - Uzbekistan 7
VE - Venezuela 7
AE - Emirati Arabi Uniti 6
IL - Israele 6
JO - Giordania 6
AU - Australia 5
EG - Egitto 5
KE - Kenya 5
LT - Lituania 5
MA - Marocco 5
BG - Bulgaria 4
CH - Svizzera 4
DO - Repubblica Dominicana 4
MY - Malesia 4
AZ - Azerbaigian 3
EU - Europa 3
QA - Qatar 3
TN - Tunisia 3
TW - Taiwan 3
AL - Albania 2
DK - Danimarca 2
DM - Dominica 2
EE - Estonia 2
GD - Grenada 2
HU - Ungheria 2
KZ - Kazakistan 2
LB - Libano 2
LV - Lettonia 2
NG - Nigeria 2
NP - Nepal 2
OM - Oman 2
PY - Paraguay 2
RO - Romania 2
RS - Serbia 2
SY - Repubblica araba siriana 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AO - Angola 1
AW - Aruba 1
BY - Bielorussia 1
BZ - Belize 1
DZ - Algeria 1
GA - Gabon 1
GE - Georgia 1
GR - Grecia 1
GY - Guiana 1
HN - Honduras 1
LK - Sri Lanka 1
NZ - Nuova Zelanda 1
PA - Panama 1
PS - Palestinian Territory 1
SC - Seychelles 1
TH - Thailandia 1
TL - Timor Orientale 1
UY - Uruguay 1
Totale 39.822
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Città #
Woodbridge 8.389
Wilmington 8.102
Houston 7.431
Fairfield 1.102
Singapore 1.002
Ashburn 740
Ann Arbor 679
Chandler 525
Seattle 509
Hong Kong 432
Beijing 397
Cambridge 374
Dublin 357
Jacksonville 349
Medford 252
Rome 213
Santa Clara 192
Dearborn 191
The Dalles 144
New York 137
Los Angeles 131
Lawrence 115
Munich 96
Zhengzhou 93
Buffalo 91
Dallas 66
Milan 66
San Diego 66
São Paulo 60
Council Bluffs 57
Chicago 54
Menlo Park 52
Ho Chi Minh City 48
Nuremberg 46
Moscow 39
London 36
Mülheim 36
Engelhard 32
Hanoi 31
Jakarta 28
Brussels 27
Shanghai 27
Phoenix 26
Redondo Beach 25
Brooklyn 24
Center 24
Hefei 24
Nanjing 23
Redwood City 23
Montreal 22
Tokyo 22
Dong Ket 21
Pune 21
Warsaw 20
Boardman 19
Poplar 19
San Mateo 19
Chennai 18
Falls Church 18
Mountain View 18
Salt Lake City 18
Seoul 18
Florence 17
Frankfurt am Main 17
St. George 17
Vienna 17
Atlanta 16
Denver 16
Helsinki 16
Norwalk 16
Toronto 16
Turku 16
University Park 16
Bologna 15
Chongqing 15
Amsterdam 14
Ankara 14
Elk Grove Village 14
Rio de Janeiro 14
Stockholm 14
Orem 13
Verona 13
Brno 12
Del Norte 12
Johannesburg 12
Turin 12
Manchester 11
San Francisco 11
Baghdad 10
Barcelona 10
Nanchang 10
Palo Alto 10
Porto Alegre 10
Biên Hòa 9
Fortaleza 9
Hangzhou 9
Mexico City 9
San Jose 9
Buenos Aires 8
Catania 8
Totale 33.723
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Nome #
Fulminant Fusobacterium necrophorum meningitis in an immunocompetent adolescent 558
Chronic granulomatous disease: Clinical, molecular, and therapeutic aspects 509
A 2-month-old male with pyuria and persistent fever 493
Bruton's tyrosine kinase defect in dendritic cells from X-linked agammaglobulinaemia patients does not influence their differentiation, maturation and antigen-presenting cell function 487
Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency 486
A 13-year-old girl with recurrent inguinal lymphadenopathy. 481
Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome. 479
Immunodeficiency in Vici Syndrome: a Heterogeneous Phenotype 478
Clinical features and follow-up in patients with 22q11.2 deletion syndrome 475
Rh system and intrauterine growth. Interaction with season of birth 468
Chronic Granulomatous Disease Presenting with Salmonella Brain Abscesses. 468
Hereditary Deficiency of gp91(phox) Is Associated With Enhanced Arterial Dilatation Results of a Multicenter Study 464
Does NADPH oxidase deficiency cause artery dilatation in humans? 461
Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy 461
Pancytopenia and severe sepsis in an adult case of congenital X-linked agammaglobulinemia (XLA) 460
Transitory hypogammaglobulinemia of infancy in FG syndrome [2] 455
Dual-regulated lentiviral vector for gene therapy of X-linked chronic granulomatosis 454
Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: An Italian multicenter study 450
Rapid T-cell receptor CD4+ repertoire reconstitution and immune recovery in unrelated umbilical cord blood transplanted pediatric leukemia patients 446
Intra-Erythrocyte Infusion of Dexamethasone Reduces Neurological Symptoms in Ataxia Teleangiectasia Patients: Results of a Phase 2 Trial. 444
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 444
Visceral leishmaniasis revealing chronic granulomatous diseases in a child 443
Lack of iNKT cells in patients with combined immune deficiency due to hypomorphic RAG mutations 441
The impact of TACI mutations: from hypogammaglobulinemia in infancy to autoimmunity in adulthood 441
The Quality of Life of Children and Adolescents with X-Linked Agammaglobulinemia 439
Etiology, clinical outcome, and laboratory features in children with neutropenia: analysis of 104 cases 437
Role of reduced intensity conditioning in T-cell and B-cell immune reconstitution after HLA-identical bone marrow transplantation in ADA-SCID 434
Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: An Italian multicenter study 433
Reduced Atherosclerotic Burden in Subjects With Genetically Determined Low Oxidative Stress 433
Relapsing Campylobacter jejuni Systemic Infections in a Child with X-Linked Agammaglobulinemia 433
Inherited human gp91phox deficiency is associated with impaired isoprostane formation and platelet dysfunction 429
gp91phox-dependent expression of platelet CD40 ligand 426
Serum soluble ST2 as diagnostic marker of systemic inflammatory reactive syndrome of bacterial etiology in children. 424
. Serum Soluble ST2 as Diagnostic Marker of Systemic Inflammatory Reactive Syndrome of Bacterial Etiology in Children. 424
Preclinical safety and efficacy of human CD34(+) cells transduced with lentiviral vector for the treatment of Wiskott-Aldrich syndrome 416
Pancytopenia and severe sepsis in an adult case of congenital X-linked agammaglobulinemia (XLA). 413
X-chromosome inactivation and mutation pattern in the Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinemia. Italian XLA Collaborative Group 407
The impact of TACI mutations in children affected with hypogammaglobulinemia and in their relatives with autoimmunity: a matter of age. 406
Defective B-cell proliferation and maintenance of long-term memory in patients with chronic granulomatous disease 403
“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 403
Successful treatment with percutaneous transhepatic alcoholization of a liver abscess in a child with chronic granulomatous disease 402
Effectiveness of immunoglobulin replacement therapy on clinical outcome in patients with primary antibody deficiencies: results from a multicenter prospective cohort study 398
Shift from intravenous or 16% subcutaneous replacement therapy to 20% subcutaneous immunoglobulin in patients with primary antibody deficiencies 396
Evaluation of the relevance of humoral immunodeficiencies in a pediatric population affected by recurrent infections 395
Serratia marcescens Osteomyelitis in a Newborn with Chronic Granulomatous 395
Subcutaneous Immunoglobulin Replacement Therapy in Patients with Primary Immunodeficiency in Routine Clinical Practice: The VISPO Prospective Multicenter Study 394
Different degrees of NADPH oxidase 2 regulation and in vivo platelet activation: lesson from chronic granulomatous disease 389
Non invasive assessment of lung disease in ataxia telangiectasia by high-field magnetic resonance imaging 389
Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience 383
Nox2 is determinant for ischemia-induced oxidative stress and arterial vasodilatation: a pilot study in patients with hereditary Nox2 deficiency 381
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia 380
X-linked Lymphoproliferative Disease due to SAP/SH2D1A deficiency: A Multicentre Study on the manifestations, management and outcome of the disease 380
Post-natal ontogenesis of the T-cell receptor CD4 and CD8 V beta repertoire and immune function in children with DiGeorge syndrome 379
How should eosinophilic cystitis be treated in patients with chronic granulomatous disease? 378
[Goiter prevalence and urinary excretion of iodine in a sample of school age children in the city of Rome] 377
Humoral immune responses and CD27+B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome) 374
Consanguinity and polygenic diseases: a model for antibody deficiencies 374
Caratterizzazione clinica di pazienti con ipogammaglobulinemia. 366
Hyper Ige syndrome(HIES):description of patients with different clinical and molecular phenotype. 362
Clinical characterization of hypogammaglobulinemia. 360
Immunodeficiency in Vici syndrome: a heterogeneous phenotype 357
HLA-haploidentical stem cell transplantation after removal of αβ+ T and B cells in children with nonmalignant disorders 356
Molecular characterization of TNFRSF13B gene in pediatric patients with hypogammaglobulinemia. 356
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 355
Caratterizzazione genetica di pazienti pediatrici con ipogammaglobulinemia. 353
Familial Hemophagocytic Lymphohistiocytosis Type 3 Diagnosed at School Age: A Case Report 352
Outcome of hematopoietic stem cell transplantation for adenosine deaminase-deficient severe combined immunodeficiency 352
Evidence of clonotypic pattern of T-cell repertoire in synovial fluid of children with juvenile rheumatoid arthritis at the onset of the disease 347
Parvovirus(PV B19) infection and juvenile chronic arthritis 344
Cutaneous granulomatosis and combined immunodeficiency revealing Ataxia-Telangiectasia: a case report 337
Dermatite non solo atopica: descrizione di due casi di sindrome da Iper IgE (HIES) 331
Late-onset combined immune-deficiency due to LIGIV mutations in a 12 years old patient 331
Parvovirus (PV B19) infection and juvenile chronic arthritis 329
Evidence of clonotypic pattern of T cell repertoire in synovial fluid of children with juvenile rheumatoid arthritis at the onset of the disease. 312
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. 298
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 294
Immunoglobulin subclasses and specific antihemophilus influentiae response in children with recurrent infections 278
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 263
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 219
First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia 209
The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment 204
Phenotypical T Cell Differentiation Analysis: A Diagnostic and Predictive Tool in the Study of Primary Immunodeficiencies 198
Characterization of T and B cell repertoire diversity in patients with RAG deficiency 197
Diagnostic Approach to Monogenic Inflammatory Bowel Disease in Clinical Practice: A Ten-Year Multicentric Experience 195
Impaired X-CGD T cell compartment is gp91phox-NADPH oxidase independent 192
Autoimmune neutropenia of childhood secondary to other autoimmune disorders: Data from the Italian neutropenia registry 191
Idiopathic neutropenia of infancy: Data from the Italian Neutropenia Registry 189
Urogenital Abnormalities in Adenosine Deaminase Deficiency 184
PEDIATRIA 183
The Interplay between CD27dull and CD27bright B Cells Ensures the Flexibility, Stability, and Resilience of Human B Cell Memory 181
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) 179
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 176
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. 173
Waning of vaccine-induced immunity to measles in kidney transplanted children 172
Evaluation of mother’s stress during hospitalization can influence the breastfeeding rate. Experience in intensive and non intensive departments 171
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) 168
Fungal infections of the lung in children 168
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function 167
Immunotherapy with an HIV-DNA vaccine in children and adults 167
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection 161
Totale 35.647
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Categoria #
all - tutte 104.342
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 104.342
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212.871 0 0 0 0 0 654 778 735 202 182 216 104
2021/20221.330 56 165 84 67 93 95 58 58 150 88 76 340
2022/20231.596 153 123 42 186 94 436 182 118 128 5 92 37
2023/2024829 80 74 37 34 65 185 80 58 27 10 43 136
2024/20253.923 126 892 407 222 162 270 307 167 337 339 429 265
2025/20262.870 545 323 633 569 609 191 0 0 0 0 0 0
Totale 40.276