IRIS
CICALESE, MARIA PIA
 Distribuzione geografica
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Continente #
EU - Europa 2.754
AS - Asia 2.444
NA - Nord America 1.978
SA - Sud America 576
AF - Africa 78
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 4
Totale 7.846
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Nazione #
US - Stati Uniti d'America 1.876
RU - Federazione Russa 1.533
SG - Singapore 915
CN - Cina 756
BR - Brasile 468
IT - Italia 331
SE - Svezia 292
HK - Hong Kong 257
VN - Vietnam 236
DE - Germania 137
FR - Francia 115
GB - Regno Unito 105
IN - India 82
CA - Canada 61
AT - Austria 44
AR - Argentina 40
PL - Polonia 34
FI - Finlandia 32
JP - Giappone 32
ES - Italia 31
MX - Messico 31
NL - Olanda 31
ZA - Sudafrica 27
BD - Bangladesh 24
IQ - Iraq 24
TR - Turchia 24
EC - Ecuador 20
CO - Colombia 15
ID - Indonesia 14
LT - Lituania 14
IE - Irlanda 13
UA - Ucraina 13
DZ - Algeria 10
AU - Australia 9
UY - Uruguay 9
BE - Belgio 8
IL - Israele 8
IR - Iran 8
KE - Kenya 7
PE - Perù 7
SA - Arabia Saudita 7
UZ - Uzbekistan 7
ET - Etiopia 6
KR - Corea 6
MA - Marocco 6
PK - Pakistan 6
VE - Venezuela 6
AE - Emirati Arabi Uniti 5
BG - Bulgaria 5
CH - Svizzera 5
EG - Egitto 5
PY - Paraguay 5
TN - Tunisia 5
EU - Europa 4
MY - Malesia 4
NG - Nigeria 4
CI - Costa d'Avorio 3
CL - Cile 3
CZ - Repubblica Ceca 3
DO - Repubblica Dominicana 3
JO - Giordania 3
KZ - Kazakistan 3
NP - Nepal 3
CY - Cipro 2
JM - Giamaica 2
KW - Kuwait 2
LB - Libano 2
NZ - Nuova Zelanda 2
OM - Oman 2
PH - Filippine 2
PR - Porto Rico 2
PS - Palestinian Territory 2
RO - Romania 2
SN - Senegal 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
AM - Armenia 1
AO - Angola 1
AZ - Azerbaigian 1
BH - Bahrain 1
BO - Bolivia 1
DK - Danimarca 1
GR - Grecia 1
GY - Guiana 1
HN - Honduras 1
KG - Kirghizistan 1
LV - Lettonia 1
MK - Macedonia 1
ML - Mali 1
MT - Malta 1
NA - Namibia 1
NR - Nauru 1
PT - Portogallo 1
QA - Qatar 1
SR - Suriname 1
TJ - Tagikistan 1
Totale 7.846
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Città #
Singapore 499
Moscow 313
Hong Kong 253
Ashburn 245
Dallas 245
Shanghai 184
San Jose 176
New York 144
Beijing 107
Hefei 101
Milan 85
Lauterbourg 84
Ho Chi Minh City 82
Lawrence 78
Princeton 78
Los Angeles 63
São Paulo 53
Hanoi 49
Rome 39
Nuremberg 36
Munich 35
Orem 34
Boardman 33
Denver 29
Warsaw 29
Santa Clara 28
Tokyo 28
Chennai 25
London 25
Guangzhou 23
Poplar 22
Brooklyn 21
Helsinki 20
Stockholm 20
Vienna 20
Chicago 19
Brescia 18
Cesano Boscone 18
Montreal 17
Toronto 17
Frankfurt am Main 16
Johannesburg 16
Atlanta 15
Rio de Janeiro 15
Seattle 15
Ankara 13
Council Bluffs 13
Houston 13
Mexico City 13
Phoenix 13
Haiphong 12
Pune 12
Shenzhen 12
The Dalles 12
Amsterdam 11
Da Nang 10
Dublin 10
Hangzhou 10
Madrid 10
Monza 10
Turin 10
Curitiba 9
Manchester 9
Mumbai 9
Paris 9
Belo Horizonte 8
Boston 8
Brasília 8
Montevideo 8
Salvador 8
Biên Hòa 7
Cambridge 7
Falkenstein 7
Guayaquil 7
Lima 7
Sorocaba 7
Tashkent 7
Turku 7
Calgary 6
Columbus 6
Fortaleza 6
Milwaukee 6
Nairobi 6
New Delhi 6
Philadelphia 6
Tianjin 6
Washington 6
Aksum 5
Barnet 5
Bengaluru 5
Bogotá 5
Brisbane 5
Changsha 5
Charlotte 5
Florence 5
Guarulhos 5
Hillah 5
Lappeenranta 5
Naples 5
Porto Alegre 5
Totale 3.907
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Nome #
Lentiviral hematopoietic stem cell gene therapy benefits metachromatic leukodystrophy 372
Reduced PD-1 expression on circulating follicular and conventional FOXP3+ Treg cells in children with new onset type 1 diabetes and autoantibody-positive at-risk children 178
Lentiviral haematopoietic stem-cell gene therapy for early-onset metachromatic leukodystrophy: long-term results from a non-randomised, open-label, phase 1/2 trial and expanded access 161
A case of T-cell acute lymphoblastic leukemia in retroviral gene therapy for ADA-SCID 158
A Novel Assay in Whole Blood Demonstrates Restoration of Mitochondrial Activity in Phagocytes After Successful HSCT in Hyperinflamed X-Linked Chronic Granulomatous Disease 145
Case Report: Consistent disease manifestations with a staggered time course in two identical twins affected by adenosine deaminase 2 deficiency 135
A novel genomic inversion in Wiskott-Aldrich-associated autoinflammation 133
Hematopoietic stem-and progenitor-cell gene therapy for hurler syndrome 133
Genetic determinants of type 1 diabetes in individuals with weak evidence of islet autoimmunity at disease onset 129
Bone marrow harvesting from paediatric patients undergoing haematopoietic stem cell gene therapy 126
Early skeletal outcomes after hematopoietic stem and progenitor cell gene therapy for Hurler syndrome 123
Efficacy and safety of an amino-acid-based formula during the period of weaning children with intestinal failure and parenteral nutrition 119
Follicular helper T cell signature of replicative exhaustion, apoptosis and senescence in common variable immunodeficiency 117
Peripheral blood stem and progenitor cell collection in pediatric candidates for ex vivo gene therapy: a 10-year series 116
Long-term and real-world safety and efficacy of retroviral gene therapy for adenosine deaminase deficiency 113
A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency 109
Clinical outcome, incidence, and SARS-CoV-2 infection-fatality rates in Italian patients with inborn errors of immunity 109
Abnormalities of acid-base balance and predisposition to metabolic acidosis in Metachromatic Leukodystrophy patients 107
ALPS-Like Phenotype Caused by ADA2 Deficiency Rescued by Allogeneic Hematopoietic Stem Cell Transplantation 107
COVID-19 in recipients of allogeneic stem cell transplantation: favorable outcome 107
Wiskott–Aldrich syndrome: Oral findings and microbiota in children and review of the literature 105
A Case of Two Adult Brothers with Wiskott-Aldrich Syndrome, One Treated with Gene Therapy and One with HLA-Identical Hematopoietic Stem Cell Transplantation 104
A Prevalent CXCR3+ Phenotype of Circulating Follicular Helper T Cells Indicates Humoral Dysregulation in Children with Down Syndrome 103
Up to 10.5 Years of Follow-Up in 17 Subjects Treated with Hematopoietic Stem and Progenitor Cell Lentiviral Gene Therapy for Wiskott-Aldrich Syndrome 99
Hematopoietic reconstitution dynamics of mobilized- and bone marrow-derived human hematopoietic stem cells after gene therapy 99
Pioglitazone as a novel therapeutic approach in chronic granulomatous disease 99
Correction to: A Case of Two Adult Brothers with Wiskott‑Aldrich Syndrome, One Treated with Gene Therapy and One with HLA‑Identical Hematopoietic Stem Cell Transplantation (Journal of Clinical Immunology, (2022), 42, 2, (421-425), 10.1007/s10875-021-01157-6) 98
Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies 98
T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency 94
Mild SARS-CoV-2 Infection After Gene Therapy in a Child With Wiskott-Aldrich Syndrome: A Case Report 93
Reduced Follicular Regulatory T Cells in Spleen and Pancreatic Lymph Nodes of Patients With Type 1 Diabetes 91
B-cell development and functions and therapeutic options in adenosine deaminase-deficient patients 90
Lentiviral correction of enzymatic activity restrains macrophage inflammation in adenosine deaminase 2 deficiency 89
Natural history of type 1 diabetes on an immunodysregulatory background with genetic alteration in B-cell activating factor receptor: A case report 85
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 85
Circulating follicular helper and follicular regulatory T cells are severely compromised in human CD40 deficiency: A case report 84
Emapalumab treatment in an ADA-SCID patient with refractory hemophagocytic lymphohistiocytosis-related graft failure and disseminated BCGitis 84
Beta2 integrins are required for follicular helper T cell differentiation in humans 83
The EHA Research Roadmap: Hematopoietic Stem Cell Gene Therapy 82
Third cranial nerve palsy in an 88-year-old man after SARS-CoV-2 mRNA vaccination: Change of injection site and type of vaccine resulted in an uneventful second dose with humoral immune response 81
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 80
Long-Term Effects of Atidarsagene Autotemcel for Metachromatic Leukodystrophy 80
Immunosuppressive therapy in childhood‐onset arrhythmogenic inflammatory cardiomyopathy 79
Urogenital Abnormalities in Adenosine Deaminase Deficiency 78
Deconstructing IgG4-related disease involvement of midline structures: Comparison to common mimickers. 77
Central venous access devices in pediatric malignancies: a position paper of Italian Association of Pediatric Hematology and Oncology 76
Persistence of circulating T-follicular helper cells after rituximab is associated with relapse of IgG4-related disease 76
Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndrome 74
Clinical applications of gene therapy for primary immunodeficiencies 74
Lentiviral haemopoietic stem/progenitor cell gene therapy for treatment of Wiskott-Aldrich syndrome: interim results of a non-randomised, open-label, phase 1/2 clinical study 71
Lentiviral haemopoietic stem-cell gene therapy in early-onset metachromatic leukodystrophy: an ad-hoc analysis of a non-randomised, open-label, phase 1/2 trial 71
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy 70
Treatment with rapamycin can restore regulatory T-cell function in IPEX patients 69
Dynamics of genetically engineered hematopoietic stem and progenitor cells after autologous transplantation in humans 68
Telemedicine in myocarditis: Evolution of a mutidisciplinary “disease unit” at the time of COVID-19 pandemic 68
Intrabone hematopoietic stem cell gene therapy for adult and pediatric patients affected by transfusion-dependent ß-thalassemia 67
Update on the safety and efficacy of retroviral gene therapy for immunodeficiency due to adenosine deaminase deficiency 65
In Vivo Tracking of Human Hematopoiesis Reveals Patterns of Clonal Dynamics during Early and Steady-State Reconstitution Phases 65
Correction to: Hematopoietic Cell Transplantation Cures Adenosine Deaminase 2 Deficiency: Report on 30 Patients (Journal of Clinical Immunology, (2021), 41, 7, (1633-1647), 10.1007/s10875-021-01098-0) 61
Pediatric cancer care management during the COVID-19 pandemic: a review of the literature and a single-centre real-life experience of an Italian pediatric oncology unit 61
Gene therapy in rare diseases: The benefits and challenges of developing a patient-centric registry for Strimvelis in ADA-SCID 61
EFFICACY OF THE ANDRESEN ACTIVATOR BEFORE PEAK GROWTH IN CLASS II PATIENTS 61
Hematopoietic Cell Transplantation Cures Adenosine Deaminase 2 Deficiency: Report on 30 Patients 61
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 60
NADPH Oxidase Deficiency: A Multisystem Approach 59
T regulatory cell therapy in preclinical and clinical pancreatic islet transplantation 58
Longitudinal MRI quantification of muscle degeneration in Duchenne muscular dystrophy 57
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet) 57
Human IL2RA null mutation mediates immunodeficiency with lymphoproliferation and autoimmunity 56
New perspectives in gene therapy for inherited disorders 56
Rubella Virus Infected Macrophages and Neutrophils Define Patterns of Granulomatous Inflammation in Inborn and Acquired Errors of Immunity 56
Purine metabolism, immune reconstitution, and abdominal adipose tumor after gene therapy for adenosine deaminase deficiency 55
Successful use of long-acting octreotide for intractable chronic gastrointestinal bleeding in children 55
Neutrophils drive type-I interferon production and autoantibodies in Wiskott-Aldrich syndrome 55
LENTIVIRAL VECTOR TRANSDUCED CD34+CELLS FOR THE TREATMENT OF WISKOTT-ALDRICH SYNDROME 55
Successful Treatment With Ledipasvir/Sofosbuvir in an Infant With Severe Combined Immunodeficiency Caused by Adenosine Deaminase Deficiency With HCV Allowed Gene Therapy with Strimvelis 54
Risk of seizures in children receiving busulphan-containing regimens for stem cell transplantation 54
Harnessing Type I IFN Immunity Against SARS-CoV-2 with Early Administration of IFN-β 54
Editorial: Follicular Helper T Cells in Immunity and Autoimmunity 53
Inflammation Converts Human Mesoangioblasts Into Targets of Alloreactive Immune Responses: Implications for Allogeneic Cell Therapy of DMD 51
First occurrence of plasmablastic lymphoma in adenosine deaminase-deficient severe combined immunodeficiency disease patient and review of the literature 50
Use of Defibrotide to help prevent post-transplant endothelial injury in a genetically predisposed infant with metachromatic leukodystrophy undergoing hematopoietic stem cell gene therapy 50
Gene Therapy for Adenosine Deaminase Deficiency: A Comprehensive Evaluation of Short- and Medium-Term Safety 49
Guidelines for the use of long-term central venous catheter in children with hemato-oncological disorders. On behalf of supportive therapy working group of Italian Association of Pediatric Hematology and Oncology (AIEOP) 49
La mucosite post-chemioterapia in bambini sottoposti a terapia genica, l'esperienza del San Raffaele di Milano 48
Lentiviral gene therapy corrects platelet phenotype and function in Wiskott-Aldrich patients 48
Treatment of chronic hepatitis C in children with pegylated interferon and ribavirin : the impact of dose 48
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for diagnosing inborn errors of immunity 47
SARS-CoV-2 infection and treatment in a cohort of patients with inborn errors of immunity 47
Relationship between severe obesity and gut inflammation in children: what’s next? 47
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy 46
Requesting iodine supplementation in children on parenteral nutrition 45
NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential 44
Single-day trimethoprim/sulfamethoxazole prophylaxis for Pneumocystis pneumonia in children with cancer 44
Gene therapy trial with lentiviral vector transduced CD34+cells for the treatment of Wiskott-Aldrich Syndrome 40
CXCR5-CXCL13 axis markers in full-term and preterm human neonates in the first weeks of life 40
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects 37
Management of autoimmune hepatitis in children: how many steps away from common agreement? 36
Hemophagocytic inflammatory syndrome in ADA-SCID: report of two cases and literature review 9
Early bone marrow alterations in patients with adenosine deaminase 2 deficiency across disease phenotypes and severities 9
Totale 8.034
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Categoria #
all - tutte 43.046
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 43.046
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211 0 0 0 0 0 0 0 0 0 1 0 0
2021/202286 0 0 1 13 6 3 8 9 33 4 6 3
2022/2023588 171 113 47 4 11 67 18 56 37 15 27 22
2023/2024604 47 33 59 69 47 100 29 43 5 28 25 119
2024/20251.762 161 42 66 75 76 130 214 227 282 193 120 176
2025/20264.928 347 340 431 733 460 188 437 384 1.365 243 0 0
Totale 8.052