IRIS
CASALE, Maddalena
 Distribuzione geografica
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Continente #
EU - Europa 4.980
AS - Asia 1.848
NA - Nord America 1.751
SA - Sud America 379
AF - Africa 34
Totale 8.992
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Nazione #
RU - Federazione Russa 3.419
US - Stati Uniti d'America 1.714
SG - Singapore 772
IE - Irlanda 499
CN - Cina 445
IT - Italia 424
BR - Brasile 317
HK - Hong Kong 264
DE - Germania 160
GB - Regno Unito 155
KR - Corea 97
UA - Ucraina 94
VN - Vietnam 91
GR - Grecia 46
IN - India 46
JP - Giappone 38
FR - Francia 37
SE - Svezia 32
FI - Finlandia 31
AR - Argentina 29
AT - Austria 24
TR - Turchia 23
CA - Canada 16
MX - Messico 16
PK - Pakistan 15
BE - Belgio 13
NL - Olanda 12
ZA - Sudafrica 11
ID - Indonesia 9
BD - Bangladesh 8
CH - Svizzera 8
IQ - Iraq 8
CO - Colombia 7
DZ - Algeria 7
PY - Paraguay 7
CL - Cile 6
EC - Ecuador 6
UZ - Uzbekistan 6
KE - Kenya 5
VE - Venezuela 5
CZ - Repubblica Ceca 4
ES - Italia 3
IR - Iran 3
JO - Giordania 3
KZ - Kazakistan 3
LB - Libano 3
MA - Marocco 3
PT - Portogallo 3
RS - Serbia 3
AE - Emirati Arabi Uniti 2
DO - Repubblica Dominicana 2
EG - Egitto 2
MK - Macedonia 2
PL - Polonia 2
SA - Arabia Saudita 2
TN - Tunisia 2
UY - Uruguay 2
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BG - Bulgaria 1
BH - Bahrain 1
BS - Bahamas 1
CY - Cipro 1
DK - Danimarca 1
ET - Etiopia 1
GA - Gabon 1
GE - Georgia 1
GT - Guatemala 1
HU - Ungheria 1
IL - Israele 1
KG - Kirghizistan 1
LT - Lituania 1
LU - Lussemburgo 1
MD - Moldavia 1
NG - Nigeria 1
PH - Filippine 1
PS - Palestinian Territory 1
RO - Romania 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
TW - Taiwan 1
Totale 8.992
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Città #
Moscow 1.175
Dublin 487
Singapore 342
Santa Clara 294
Hong Kong 264
Chandler 231
Jacksonville 189
Seoul 97
Beijing 90
Ann Arbor 88
Hefei 71
Bremen 70
Princeton 70
Caserta 69
Roxbury 66
Ashburn 53
Medford 51
Naples 48
New York 40
Dallas 39
The Dalles 37
Bengaluru 36
Woodbridge 35
Ho Chi Minh City 32
São Paulo 31
Munich 28
Nanjing 25
Wilmington 25
Ercolano 23
Des Moines 22
Boardman 21
Cambridge 19
Rome 18
Grumo Nevano 17
Hanoi 17
Napoli 16
Vienna 15
Brussels 13
Helsinki 11
Nuremberg 11
Los Angeles 10
Belo Horizonte 9
Falkenstein 9
Haiphong 9
San Mateo 9
Boston 8
Curitiba 8
Johannesburg 8
Pozzuoli 8
Brasília 7
Brooklyn 7
Milan 7
Nanchang 7
Nocera Inferiore 7
Redwood City 7
Rio de Janeiro 7
Fairfield 6
Istanbul 6
Mexico City 6
Mountain View 6
Seattle 6
Shenyang 6
Tashkent 6
Tianjin 6
Turku 6
Asunción 5
Campinas 5
Da Nang 5
Elora 5
Kunming 5
London 5
Nairobi 5
Orlando 5
Salvador 5
San Sebastiano al Vesuvio 5
Shanghai 5
Stella Cilento 5
Amsterdam 4
Auburn Hills 4
Aversa 4
Biên Hòa 4
Brno 4
Buenos Aires 4
Changchun 4
Guangzhou 4
Houston 4
Lappeenranta 4
Mumbai 4
Nemoli 4
Pagani 4
Porto Alegre 4
Quito 4
Ribeirão Preto 4
Santiago 4
Shenzhen 4
Amman 3
Ankara 3
Atlanta 3
Bandung 3
Belgrade 3
Totale 4.614
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Nome #
Cognitive, Brain and Intracranial Artery Involvement in Beta Thalassemia 201
Effects of germline VHL deficiency on growth, metabolism, and mitochondria 200
Blood transfusions and adverse acute events: a retrospective study from 214 transfusion-dependent pediatric patients comparing transfused blood components by apheresis or by whole blood 167
HNF-1β mutation affects PKD2 and SOCS3 expression causing renal cysts and diabetes in MODY5 kindred. 166
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range. 160
Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overload 156
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation) 155
Endocrine function and bone disease during long-term chelation therapy with deferasirox in patients with β-thalassemia major. 154
Asymptomatic intracranial aneurysms in beta-thalassemia: A three-year follow-up report 148
Brain iron content in systemic iron overload: A beta-thalassemia quantitative MRI study 145
A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil Deformity 142
Clinical outcome of transfusions with extended red blood cell matching in β-thalassemia patients: A single-center experience 137
Brain functional impairment in beta-thalassaemia: the cognitive profile in Italian neurologically asymptomatic adult patients in comparison to the reported literature 135
Acute events in children with sickle cell disease in Italy during the COVID-19 pandemic: useful lessons learned 132
BONE MINERAL DENSITY IMPROVEMENT IN PATIENTS WITH THALASSEMIA MAJOR ON LONG-TERM CHELATION THERAPY WITH DEFERASIROX 131
Cb2 receptor stimulation and dexamethasone restore the anti-inflammatory and immune-regulatory properties of mesenchymal stromal cells of children with immune thrombocytopenia 130
No evidence of increased cerebrovascular involvement in adult neurologically-asymptomatic β-Thalassaemia. A multicentre multimodal magnetic resonance study 128
Association of immune thrombocytopenia and celiac disease in children: A retrospective case control study 128
Risk factors for endocrine complications in transfusion-dependent thalassemia patients on chelation therapy with deferasirox: a risk assessment study from a multicentre nation-wide cohort 125
[The Management of Endocrine Complications in Patients with Haemoglobinopathies: Good Clinical Practice of the Italian Society of Thalassemia and Haemoglobinopathies (SITE).] 124
Congenital Dyserythropoietic Anemia Type II: molecular analysis and expression of the SEC23B Gene. 122
National systematic approach to the management of asplenia: the set up of the Italian Network on Asplenia 121
An Educational Study Promoting the Delivery of Transcranial Doppler Ultrasound Screening in Paediatric Sickle Cell Disease: A European Multi-Centre Perspective 120
Childhood Multiple Endocrine Neoplasia (MEN) Syndromes: Genetics, Clinical Heterogeneity and Modifying Genes 117
Association between serum ferritin and liver iron concentration with cardiac iron in pediatric thalassemia major patients 116
Access to emergency department for acute events and identification of sickle cell disease in refugees. 115
Long-term improvement in cardiac magnetic resonance in β-thalassemia major patients treated with deferasirox extends to patients with abnormal baseline cardiac function 114
Transient erythroblastopenia of childhood after COVID-19 infection: a case report 113
Absence of blood donors’ anti-SARS-CoV-2 antibodies in pre-storage leukoreduced red blood cell units indicates no role of passive immunity for blood recipients 109
Headache in beta-thalassemia: An Italian multicenter clinical, conventional MRI and MR-angiography case-control study 107
Long-term efficacy of deferasirox for cardiac siderosis in thalassemia major 105
Clinical and molecular spectrum of glucose-6-phosphate isomerase deficiency. Report of 12 new cases 105
Rubrica a cura di luciano de seta quando il saturimetro mente… 100
Predicting factors for liver iron overload at the first magnetic resonance in children with thalassaemia major 98
Deferasirox: la chelazione ottimale nelle anemie trasfusione-dipendenti 98
Long term efficacy of iron chelation therapy with deferasirox on endocrine function in thalassemia major 95
Longitudinal Prospective MRI Study in Pediatric Patients With Thalassemia Major 95
Iron chelating properties of Eltrombopag: Investigating its role in thalassemia-induced osteoporosis 95
Characterisation of transfusion-dependent prediabetes using continuous glucose monitoring: The Haemoglycare study 93
Organizing national responses for rare blood disorders: The Italian experience with sickle cell disease in childhood 93
Splenectomy for hereditary spherocytosis: complete, partial or not at all? 93
Tricuspid-valve regurgitant jet velocity as a risk factor for death in β-Thalassemia. 93
Life-Threatening Drug-Induced Liver Injury in a Patient with β-Thalassemia Major and Severe Iron Overload on Polypharmacy. 92
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: Analysis of 78 patients from 21 families 91
Extramedullary haematopoiesis correlates with genotype and absence of cardiac iron overload in polytransfused adults with thalassaemia 91
Hb Vanvitelli: A new unstable α-globin chain variant causes undiagnosed chronic haemolytic anaemia when co-inherited with deletion − α3.7. 90
CB2 and TRPV1 receptors in inflammatory state of macrophages from sickle cell anemia pediatric/young adults 89
Italian patients with hemoglobinopathies exhibit a 5-fold increase in age-standardized lethality due to SARS-CoV-2 infection 89
Response to measles, mumps and rubella (Mmr) vaccine in transfusion-dependent patients 88
Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene 87
No increased cerebrovascular involvement in adult beta-thalassemia by advanced MRI analyses 87
Management of the risk for severe infections in children with asplenia: Recommendations from the Italian Network of Asplenia 87
Prospective MRI study in pediatric thalassemia major (TM) patients in the MIOT network: a tool to strengthen medical decisions 86
Multiparametric Cardiac Magnetic Resonance Survey in Children With Thalassemia Major: A Multicenter Study 85
Hydroxyurea prescription, availability and use for children with sickle cell disease in Italy: Results of a National Multicenter survey. 85
Acute chest syndrome in children with sickle cell disease: Data from a national AIEOP cohort identify priority areas of intervention in a hub-and-spoke system 84
Second-line therapy in paediatric warm autoimmune haemolytic anaemia. Guidelines from the Associazione Italiana Onco-Ematologia Pediatrica (AIEOP) 84
Myocardial fibrosis by CMR LGE in a large cohort of pediatric thalassemia major patients 82
Effect of splenectomy on iron balance in patients with β-thalassemia major: a long-term follow-up 80
White matter volume changes in adult beta-thalassemia: Negligible and unrelated to anemia and cognitive performances 79
Red blood cell alloimmunisation in transfusion-dependent thalassaemia: A systematic review 78
Transfusional Approach in Multi-Ethnic Sickle Cell Patients: Real-World Practice Data From a Multicenter Survey in Italy 78
Incidence of cancer and related deaths in hemoglobinopathies: A follow-up of 4631 patients between 1970 and 2021 77
Subarachnoid haemorrhage and cerebral vasculopathy in a child with sickle cell anaemia 77
Nineteen-month-old girl with persistent fever 77
Prospective CMR Survey in Children With Thalassemia Major: Insights From a National Network 77
Disease burden and quality of life of in children with sickle cell disease in Italy: time to be considered a priority 77
Underlying disease is the main risk factor in post-splenectomy complication risk: Data from a national database 76
Nephrolithiasis in patients exposed to deferasirox and desferioxamine: probably an age-linked event with different effects on some renal parameters 76
HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype-phenotype correlation 76
Long‐term outcomes of avascular necrosis in sickle cell disease using joint‐specific patient‐reported outcome measures: Results from a multicentre study 75
Good Clinical Practice of the Italian Society of Thalassemia and Haemoglobinopathies (SITE) for the Management of Endocrine Complications in Patients with Haemoglobinopathies 75
Reply to "Hepatocellular carcinoma in thalassemia and other hemoglobinopathies" 74
Recommendations for the management of acute immune thrombocytopenia in children. A Consensus Conference from the Italian Association of Pediatric Hematology and Oncology 74
Screening for sickle cell disease by point-of-care tests in Italy: pilot study on 1000 at risk children 73
Early splenectomy in sickle cell disease: another piece of the puzzle 72
Premature aging of the immune system affects the response to SARS-CoV-2 mRNA vaccine in β-thalassemia: role of an additional dose 72
Selecting β-thalassemia Patients for Gene Therapy: A Decision-making Algorithm 72
Long-term treatment with deferiprone enhances left ventricular ejection function when compared to deferoxamine in patients with thalassemia major 71
Current challenges in the management of patients with sickle cell disease - A report of the Italian experience 71
Prevalence and mortality trends of hemoglobinopathies in Italy: a nationwide study 70
Juvenile erythrocytosis in children after liver transplantation: prevalence, risk factors and outcome 67
Thalassemia-Associated mixed hypogonadism (TAMH): unraveling a unique endocrine pattern and its impact on cardiovascular risk 65
Thyroid Nodule Surveillance in Transfusion-Dependent Thalassemia: A Comparative Ultrasonographic Study 65
Mortality in β-thalassemia patients with confirmed pulmonary arterial hypertension on right heart catheterization 64
Thalassaemia is paradoxically associated with a reduced risk of in-hospital complications and mortality in COVID-19: Data from an international registry 62
Will the changing therapeutic landscape meet the needs of patients with sickle cell disease? 60
Impairment of Innate Immunity and Depletion of Vaccine‐Induced Memory B and T Cells in the Absence of the Spleen 59
Manual erythroexchange in sickle cell disease: multicenter validation of a protocol predictive of volume to exchange and hemoglobin values 59
Limited access to transcranial Doppler screening and stroke prevention for children with sickle cell disease in Europe: Results of a multinational EuroBloodNet survey 57
Inflammatory and senescence-associated mediators affect the persistence of humoral response to COVID-19 mRNA vaccination in transfusion-dependent beta-thalassemic patients 55
Thalassemias and Sickle Cell Diseases in Pregnancy: SITE Good Practice 44
GROWTH ABNORMALITIES, ENDOCRINE, AND BONE DISEASE 40
FERTILITY AND PREGNANCY. In: Taher AT, Farmakis D, Porter JB, Cappellini MD, Musallam KM, eds. Guidelines for the Management of Transfusion-Dependent β-Thalassaemia (TDT). 5th ed. Nicosia, Cyprus: Thalassaemia International Federation; 2025. 38
The phenotypes of sickle cell disease: strategies to aid the identification of undiagnosed patients in the Italian landscape 31
Oxford Hip and Shoulder Scores as Potential Tools for the Early Detection of Avascular Necrosis in Apparently Unaffected Sites in Sickle Cell Disease: Results from a Prospective Cohort Study 21
null 15
Totale 9.207
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Categoria #
all - tutte 31.889
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 31.889
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021181 0 0 0 0 0 13 58 18 9 28 50 5
2021/2022465 14 0 7 9 125 31 40 21 23 21 35 139
2022/2023974 103 26 28 60 129 77 0 52 454 10 19 16
2023/2024356 30 14 14 18 132 39 2 10 4 3 28 62
2024/20251.432 10 10 10 44 212 163 244 170 223 110 129 107
2025/20264.898 234 283 332 306 556 3.187 0 0 0 0 0 0
Totale 9.207