IRIS
CANCRINI, CATERINA
 Distribuzione geografica
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Continente #
NA - Nord America 27.699
EU - Europa 2.775
AS - Asia 1.573
SA - Sud America 12
Continente sconosciuto - Info sul continente non disponibili 7
AF - Africa 3
OC - Oceania 3
Totale 32.072
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Nazione #
US - Stati Uniti d'America 27.679
SG - Singapore 981
DE - Germania 602
IT - Italia 473
IE - Irlanda 385
CN - Cina 369
UA - Ucraina 345
RU - Federazione Russa 285
SE - Svezia 185
GB - Regno Unito 174
FR - Francia 121
KR - Corea 91
FI - Finlandia 79
BE - Belgio 45
IN - India 38
KG - Kirghizistan 27
CZ - Repubblica Ceca 23
PL - Polonia 20
JP - Giappone 17
CA - Canada 16
NL - Olanda 13
IR - Iran 11
TR - Turchia 11
HK - Hong Kong 7
EU - Europa 6
VN - Vietnam 6
BR - Brasile 5
CH - Svizzera 5
AR - Argentina 4
AT - Austria 4
ES - Italia 4
AU - Australia 3
EG - Egitto 3
PH - Filippine 3
PT - Portogallo 3
HU - Ungheria 2
IL - Israele 2
MX - Messico 2
PK - Pakistan 2
RO - Romania 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
AM - Armenia 1
BD - Bangladesh 1
BG - Bulgaria 1
BY - Bielorussia 1
BZ - Belize 1
CL - Cile 1
EC - Ecuador 1
EE - Estonia 1
GR - Grecia 1
HT - Haiti 1
ID - Indonesia 1
LB - Libano 1
PE - Perù 1
QA - Qatar 1
RS - Serbia 1
SA - Arabia Saudita 1
UZ - Uzbekistan 1
Totale 32.072
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Città #
Wilmington 7.827
Woodbridge 7.574
Houston 6.207
Fairfield 878
Singapore 859
Ann Arbor 643
Chandler 580
Ashburn 446
Seattle 367
Dublin 334
Cambridge 322
Jacksonville 293
Santa Clara 248
Medford 245
Rome 181
Dearborn 177
Beijing 160
Lawrence 114
New York 108
Menlo Park 74
San Diego 71
Zhengzhou 71
Munich 46
Brussels 45
Moscow 43
Mülheim 39
Milan 36
Creede 33
Engelhard 29
Redwood City 25
Seoul 25
Boardman 24
Brno 23
Hefei 23
London 23
Pune 20
Falls Church 19
San Mateo 19
St. George 18
Verona 18
Center 17
Kraków 17
Shanghai 16
Council Bluffs 15
Nanjing 15
Los Angeles 14
Palo Alto 14
Toronto 13
Florence 12
Norwalk 12
Mountain View 11
Nürnberg 10
Guangzhou 8
Helsinki 8
Nuremberg 8
Amsterdam 7
Ankara 7
Berlin 7
Kunming 7
Naples 7
Phoenix 7
Ardabil 6
Del Norte 6
Hangzhou 6
Monte Vista 6
Nanchang 6
New Bedfont 6
Saint Petersburg 6
University Park 6
Ypsilanti 6
Chengdu 5
Dong Ket 5
Kilburn 5
Redmond 5
Shenyang 5
Shenzhen 5
Tokyo 5
Washington 5
Augusta 4
Chieti 4
Chiswick 4
Hong Kong 4
Lappeenranta 4
Leawood 4
San Francisco 4
São Paulo 4
Trieste 4
Acton 3
Auburn Hills 3
Brooklyn 3
Dallas 3
Detroit 3
Fino Mornasco 3
Genoa 3
Guidonia 3
Hounslow 3
Islington 3
Palombara Sabina 3
Prescot 3
Tappahannock 3
Totale 28.688
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Nome #
Bruton's tyrosine kinase defect in dendritic cells from X-linked agammaglobulinaemia patients does not influence their differentiation, maturation and antigen-presenting cell function 449
Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency 443
Clinical features and follow-up in patients with 22q11.2 deletion syndrome 438
NK cell effector functions in a Chédiak-Higashi patient undergoing cord blood transplantation: Effects of in vitro treatment with IL-2 438
Analysis of HIV-1 reverse transcriptase gene mutations in infected children treated with zidovudine 431
Defective dendritic cell maturation in a child with nucleotide excision repair deficiency and CD4 lymphopenia 426
Rapid T-cell receptor CD4+ repertoire reconstitution and immune recovery in unrelated umbilical cord blood transplanted pediatric leukemia patients 426
Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy 425
Early-onset monocyte-B-natural killer-dendritic cells' deficiency successfully treated with hematopoietic stem cell transplantation. 421
The Quality of Life of Children and Adolescents with X-Linked Agammaglobulinemia 421
Etiology, clinical outcome, and laboratory features in children with neutropenia: analysis of 104 cases 417
Successful allogeneic hemopoietic stem cell transplantation in a child who had anhidrotic ectodermal dysplasia with immunodeficiency 412
Role of reduced intensity conditioning in T-cell and B-cell immune reconstitution after HLA-identical bone marrow transplantation in ADA-SCID 412
The impact of TACI mutations: from hypogammaglobulinemia in infancy to autoimmunity in adulthood 411
In vivo T-cell dynamics during immune reconstitution after hematopoietic stem cell gene therapy in adenosine deaminase severe combined immune deficiency. 410
The Wiskott-Aldrich syndrome protein is required for iNKT cell maturation and function 409
Relapsing Campylobacter jejuni Systemic Infections in a Child with X-Linked Agammaglobulinemia 407
Autoimmunity and regulatory T cells in 22q11.2 deletion syndrome patients 407
Delayed early antiretroviral treatment is associated with an HIV-specific long-term cellular response in HIV-1 vertically infected infants 405
Role of immunity in maternal-infant HIV-1 transmission 405
A case of APDS patient: defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment 401
A hypermorphic I kappa B alpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency 400
Structural defects and variations in the HIV-1 nef gene from rapid, slow and non-progressor children 397
Prognostic value of a CCR5 defective allele in pediatric HIV-1 infection 396
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 396
. Early-onset monocyte-B-natural killer-dendritic cells’ deficiency successfully treated with hematopoietic stem cell transaplantation 391
Combined immunodeficiency due to JAK3 mutation in a child presenting with skin granuloma 387
Immune deficiency caused by impaired expression of nuclear factor-kappaB essential modifier (NEMO) because of a mutation in the 5' untranslated region of the NEMO gene. 386
Anti-infective prophylaxis for primary immunodeficiencies: what is done in Italian Primary Immunodeficiency Network centers (IPINet) and review of the literature 385
A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency 383
The impact of TACI mutations in children affected with hypogammaglobulinemia and in their relatives with autoimmunity: a matter of age. 381
Effectiveness of immunoglobulin replacement therapy on clinical outcome in patients with primary antibody deficiencies: results from a multicenter prospective cohort study 380
Restriction in T-cell receptor repertoire in a patient affected by trichothiodystrophy and CD4+ lymphopenia 376
Evaluation of the relevance of humoral immunodeficiencies in a pediatric population affected by recurrent infections 373
Serratia marcescens Osteomyelitis in a Newborn with Chronic Granulomatous 371
Role of parvovirus B19 infection in juvenile chronic arthritis. Is more investigation needed? 369
Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects 369
Serum leptin and CD4+ T lymphocytes in HIV+ children during highly active antiretroviral therapy 365
Successful simplification of protease inhibitor-based HAART with triple nucleoside regimens in children vertically infected with HIV 361
Consanguinity and polygenic diseases: a model for antibody deficiencies 360
Schimke immunosseous dysplasia: suggestions of genetic diversity 358
Clinical features and follow-up in patients with 22q11.2 deletion syndrome 358
Post-natal ontogenesis of the T-cell receptor CD4 and CD8 V beta repertoire and immune function in children with DiGeorge syndrome 352
Humoral immune responses and CD27+B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome) 351
Long-term follow-up and outcome of a large cohort of patients with common variable immunodeficiency 350
Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience 348
Erythema nodosum: A presenting sign of early onset sarcoidosis 338
Outcome of hematopoietic stem cell transplantation for adenosine deaminase-deficient severe combined immunodeficiency 332
Parvovirus(PV B19) infection and juvenile chronic arthritis 330
Hyper Ige syndrome(HIES):description of patients with different clinical and molecular phenotype. 330
Evidence of clonotypic pattern of T-cell repertoire in synovial fluid of children with juvenile rheumatoid arthritis at the onset of the disease 327
Clinical characterization of hypogammaglobulinemia. 327
Molecular characterization of TNFRSF13B gene in pediatric patients with hypogammaglobulinemia. 325
HLA-haploidentical stem cell transplantation after removal of αβ+ T and B cells in children with nonmalignant disorders 318
Cosa può nascondere una tumefazione articolare migrante? 317
null 316
Role of parvovirus B19 infection in juvenile chronic arthritis. Is more investigation needed? 310
Parvovirus (PV B19) infection and juvenile chronic arthritis 310
Late-onset combined immune-deficiency due to LIGIV mutations in a 12 years old patient 310
Caratterizzazione clinica di pazienti con ipogammaglobulinemia. 308
Caratterizzazione genetica di pazienti pediatrici con ipogammaglobulinemia. 308
Dermatite non solo atopica: descrizione di due casi di sindrome da Iper IgE (HIES) 304
[Perinatal infections of B19 Parvoviruses] 302
Patologia da superantigeni 301
Evidence of clonotypic pattern of T cell repertoire in synovial fluid of children with juvenile rheumatoid arthritis at the onset of the disease. 299
Role of parvovirus B19 infection in juvenile chronic arthritis. Is more investigation needed? 298
Kinetics of the T-cell receptor CD4 and CD8 V beta repertoire in HIV-1 vertically infected infants early treated with HAART 296
T cell receptor repertoire in Juvenile Rheumatoid Arthritis. 289
Wiskott-Aldrich syndrome protein-mediated actin dynamics control type-I interferon production in plasmacytoid. 275
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 248
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world 247
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. 246
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 179
Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome 178
Rituximab unveils hypogammaglobulinemia and immunodeficiency in children with autoimmune cytopenia 176
DNAM-1 Activating Receptor and Its Ligands: How Do Viruses Affect the NK Cell-Mediated Immune Surveillance during the Various Phases of Infection? 168
First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia 165
The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment 164
Phenotypical T Cell Differentiation Analysis: A Diagnostic and Predictive Tool in the Study of Primary Immunodeficiencies 163
Characterization of T and B cell repertoire diversity in patients with RAG deficiency 161
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 161
Diagnostic Approach to Monogenic Inflammatory Bowel Disease in Clinical Practice: A Ten-Year Multicentric Experience 158
Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency 156
Waning of vaccine-induced immunity to measles in kidney transplanted children 154
Increased proportions of γδ T lymphocytes in atypical SCID associate with disease manifestations 150
Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child with Intermittent Neutropenia 150
Efficacy and Adverse Events During Janus Kinase Inhibitor Treatment of SAVI Syndrome 149
NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential 147
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 146
Urogenital Abnormalities in Adenosine Deaminase Deficiency 144
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. 144
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection 144
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function 137
The Interplay between CD27dull and CD27bright B Cells Ensures the Flexibility, Stability, and Resilience of Human B Cell Memory 137
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) 136
Intergenerretional familial phenotypic variabiliti in 22q11.2 subjects: Multicenter study within IPINET 130
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 128
Life expectancy of adults with cerebral palsy. 123
How to dissect the plasticity of antigen specific immune response: a tissue perspective 123
Consensus of the Italian Primary Immunodeficiency Network on transition management from pediatric to adult care in patients affected with childhood-onset inborn errors of immunity 118
Totale 30.257
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Categoria #
all - tutte 79.962
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 79.962
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20205.839 0 0 0 0 595 730 694 799 907 840 627 647
2020/20215.875 644 638 597 738 617 605 772 663 180 156 193 72
2021/20221.393 57 121 75 86 114 106 41 63 214 78 78 360
2022/20231.850 170 134 51 204 108 416 186 302 132 9 95 43
2023/2024786 87 84 49 27 82 207 32 46 19 6 21 126
2024/20252.013 131 1.019 474 276 113 0 0 0 0 0 0 0
Totale 32.658