IRIS
CASALE, Maddalena
 Distribuzione geografica
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Continente #
EU - Europa 5.265
AS - Asia 2.173
NA - Nord America 2.168
SA - Sud America 397
AF - Africa 37
OC - Oceania 1
Totale 10.041
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Nazione #
RU - Federazione Russa 3.611
US - Stati Uniti d'America 2.125
SG - Singapore 851
CN - Cina 507
IE - Irlanda 506
IT - Italia 471
BR - Brasile 331
HK - Hong Kong 284
VN - Vietnam 230
DE - Germania 166
GB - Regno Unito 164
KR - Corea 98
UA - Ucraina 95
IN - India 54
GR - Grecia 46
FR - Francia 40
JP - Giappone 38
SE - Svezia 34
FI - Finlandia 33
AR - Argentina 30
AT - Austria 26
TR - Turchia 23
CA - Canada 19
MX - Messico 19
NL - Olanda 19
PK - Pakistan 17
BE - Belgio 13
IQ - Iraq 12
ZA - Sudafrica 11
BD - Bangladesh 10
CO - Colombia 9
ID - Indonesia 9
CH - Svizzera 8
DZ - Algeria 7
PY - Paraguay 7
UZ - Uzbekistan 7
CL - Cile 6
EC - Ecuador 6
VE - Venezuela 6
ES - Italia 5
JO - Giordania 5
KE - Kenya 5
CZ - Repubblica Ceca 4
LB - Libano 4
PL - Polonia 4
PT - Portogallo 4
TN - Tunisia 4
EG - Egitto 3
IR - Iran 3
KZ - Kazakistan 3
MA - Marocco 3
RS - Serbia 3
SA - Arabia Saudita 3
AE - Emirati Arabi Uniti 2
BG - Bulgaria 2
CY - Cipro 2
DO - Repubblica Dominicana 2
MK - Macedonia 2
PH - Filippine 2
SK - Slovacchia (Repubblica Slovacca) 2
UY - Uruguay 2
AU - Australia 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BH - Bahrain 1
BS - Bahamas 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
KW - Kuwait 1
LT - Lituania 1
LU - Lussemburgo 1
MD - Moldavia 1
NG - Nigeria 1
PS - Palestinian Territory 1
RO - Romania 1
SC - Seychelles 1
TH - Thailandia 1
TW - Taiwan 1
Totale 10.041
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Città #
Moscow 1.301
Dublin 492
Singapore 403
Santa Clara 304
Hong Kong 281
Chandler 231
San Jose 226
Jacksonville 189
Ashburn 120
Seoul 97
Beijing 95
Ann Arbor 88
Ho Chi Minh City 81
Hefei 71
Bremen 70
Princeton 70
Caserta 69
Roxbury 66
Naples 61
Hanoi 53
Medford 51
New York 42
Dallas 41
Bengaluru 37
The Dalles 37
Woodbridge 35
São Paulo 34
Munich 28
Nanjing 25
Wilmington 25
Des Moines 23
Ercolano 23
Boardman 21
Rome 20
Cambridge 19
Da Nang 18
Grumo Nevano 17
Los Angeles 17
Vienna 17
Napoli 16
Brussels 13
Haiphong 13
Helsinki 13
Nuremberg 12
Council Bluffs 11
Pescara 10
Belo Horizonte 9
Falkenstein 9
San Mateo 9
Boston 8
Curitiba 8
Johannesburg 8
Milan 8
Pozzuoli 8
Amsterdam 7
Atlanta 7
Brasília 7
Brooklyn 7
Nanchang 7
Nocera Inferiore 7
Redwood City 7
Rio de Janeiro 7
Tashkent 7
Fairfield 6
Hải Dương 6
Istanbul 6
London 6
Mexico City 6
Mountain View 6
Seattle 6
Shanghai 6
Shenyang 6
Tianjin 6
Turku 6
Asunción 5
Biên Hòa 5
Campinas 5
Chennai 5
Elora 5
Kunming 5
Montreal 5
Nairobi 5
Orlando 5
Salvador 5
San Sebastiano al Vesuvio 5
Stella Cilento 5
Amman 4
Auburn Hills 4
Aversa 4
Brno 4
Buenos Aires 4
Changchun 4
Chicago 4
Fortaleza 4
Frankfurt am Main 4
Guangzhou 4
Hillsboro 4
Houston 4
Islamabad 4
Lappeenranta 4
Totale 5.298
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Nome #
Effects of germline VHL deficiency on growth, metabolism, and mitochondria 215
Cognitive, Brain and Intracranial Artery Involvement in Beta Thalassemia 212
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 192
HNF-1β mutation affects PKD2 and SOCS3 expression causing renal cysts and diabetes in MODY5 kindred. 182
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range. 173
Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overload 172
Endocrine function and bone disease during long-term chelation therapy with deferasirox in patients with β-thalassemia major. 168
Asymptomatic intracranial aneurysms in beta-thalassemia: A three-year follow-up report 165
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation) 164
Brain iron content in systemic iron overload: A beta-thalassemia quantitative MRI study 154
A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil Deformity 154
Clinical outcome of transfusions with extended red blood cell matching in β-thalassemia patients: A single-center experience 149
Brain functional impairment in beta-thalassaemia: the cognitive profile in Italian neurologically asymptomatic adult patients in comparison to the reported literature 145
BONE MINERAL DENSITY IMPROVEMENT IN PATIENTS WITH THALASSEMIA MAJOR ON LONG-TERM CHELATION THERAPY WITH DEFERASIROX 144
Acute events in children with sickle cell disease in Italy during the COVID-19 pandemic: useful lessons learned 144
Congenital Dyserythropoietic Anemia Type II: molecular analysis and expression of the SEC23B Gene. 142
Cb2 receptor stimulation and dexamethasone restore the anti-inflammatory and immune-regulatory properties of mesenchymal stromal cells of children with immune thrombocytopenia 142
No evidence of increased cerebrovascular involvement in adult neurologically-asymptomatic β-Thalassaemia. A multicentre multimodal magnetic resonance study 141
Association of immune thrombocytopenia and celiac disease in children: A retrospective case control study 138
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 137
[The Management of Endocrine Complications in Patients with Haemoglobinopathies: Good Clinical Practice of the Italian Society of Thalassemia and Haemoglobinopathies (SITE).] 136
Childhood Multiple Endocrine Neoplasia (MEN) Syndromes: Genetics, Clinical Heterogeneity and Modifying Genes 136
An Educational Study Promoting the Delivery of Transcranial Doppler Ultrasound Screening in Paediatric Sickle Cell Disease: A European Multi-Centre Perspective 131
National systematic approach to the management of asplenia: the set up of the Italian Network on Asplenia 129
Transient erythroblastopenia of childhood after COVID-19 infection: a case report 128
Access to emergency department for acute events and identification of sickle cell disease in refugees. 124
Long-term improvement in cardiac magnetic resonance in β-thalassemia major patients treated with deferasirox extends to patients with abnormal baseline cardiac function 123
Headache in beta-thalassemia: An Italian multicenter clinical, conventional MRI and MR-angiography case-control study 122
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 121
Association between serum ferritin and liver iron concentration with cardiac iron in pediatric thalassemia major patients 121
Characterisation of transfusion-dependent prediabetes using continuous glucose monitoring: The Haemoglycare study 116
Clinical and molecular spectrum of glucose-6-phosphate isomerase deficiency. Report of 12 new cases 116
Long-term efficacy of deferasirox for cardiac siderosis in thalassemia major 111
Rubrica a cura di luciano de seta quando il saturimetro mente… 108
Response to measles, mumps and rubella (Mmr) vaccine in transfusion-dependent patients 108
Predicting factors for liver iron overload at the first magnetic resonance in children with thalassaemia major 106
CB2 and TRPV1 receptors in inflammatory state of macrophages from sickle cell anemia pediatric/young adults 104
Deferasirox: la chelazione ottimale nelle anemie trasfusione-dipendenti 104
Iron chelating properties of Eltrombopag: Investigating its role in thalassemia-induced osteoporosis 103
Management of the risk for severe infections in children with asplenia: Recommendations from the Italian Network of Asplenia 103
Italian patients with hemoglobinopathies exhibit a 5-fold increase in age-standardized lethality due to SARS-CoV-2 infection 103
Tricuspid-valve regurgitant jet velocity as a risk factor for death in β-Thalassemia. 102
Organizing national responses for rare blood disorders: The Italian experience with sickle cell disease in childhood 100
Splenectomy for hereditary spherocytosis: complete, partial or not at all? 100
Longitudinal Prospective MRI Study in Pediatric Patients With Thalassemia Major 100
Life-Threatening Drug-Induced Liver Injury in a Patient with β-Thalassemia Major and Severe Iron Overload on Polypharmacy. 100
Long term efficacy of iron chelation therapy with deferasirox on endocrine function in thalassemia major 99
Hb Vanvitelli: A new unstable α-globin chain variant causes undiagnosed chronic haemolytic anaemia when co-inherited with deletion − α3.7. 98
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: Analysis of 78 patients from 21 families 97
Extramedullary haematopoiesis correlates with genotype and absence of cardiac iron overload in polytransfused adults with thalassaemia 97
No increased cerebrovascular involvement in adult beta-thalassemia by advanced MRI analyses 96
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 95
Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene 95
Underlying disease is the main risk factor in post-splenectomy complication risk: Data from a national database 94
Hydroxyurea prescription, availability and use for children with sickle cell disease in Italy: Results of a National Multicenter survey. 94
Screening for sickle cell disease by point-of-care tests in Italy: pilot study on 1000 at risk children 92
Prospective MRI study in pediatric thalassemia major (TM) patients in the MIOT network: a tool to strengthen medical decisions 91
Second-line therapy in paediatric warm autoimmune haemolytic anaemia. Guidelines from the Associazione Italiana Onco-Ematologia Pediatrica (AIEOP) 91
Multiparametric Cardiac Magnetic Resonance Survey in Children With Thalassemia Major: A Multicenter Study 90
White matter volume changes in adult beta-thalassemia: Negligible and unrelated to anemia and cognitive performances 90
Selecting β-thalassemia Patients for Gene Therapy: A Decision-making Algorithm 90
Effect of splenectomy on iron balance in patients with β-thalassemia major: a long-term follow-up 87
Current challenges in the management of patients with sickle cell disease - A report of the Italian experience 87
Juvenile erythrocytosis in children after liver transplantation: prevalence, risk factors and outcome 86
Recommendations for the management of acute immune thrombocytopenia in children. A Consensus Conference from the Italian Association of Pediatric Hematology and Oncology 86
Myocardial fibrosis by CMR LGE in a large cohort of pediatric thalassemia major patients 85
Nineteen-month-old girl with persistent fever 85
Red blood cell alloimmunisation in transfusion-dependent thalassaemia: A systematic review 85
HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype-phenotype correlation 85
Long‐term outcomes of avascular necrosis in sickle cell disease using joint‐specific patient‐reported outcome measures: Results from a multicentre study 84
Incidence of cancer and related deaths in hemoglobinopathies: A follow-up of 4631 patients between 1970 and 2021 84
Disease burden and quality of life of in children with sickle cell disease in Italy: time to be considered a priority 84
Good Clinical Practice of the Italian Society of Thalassemia and Haemoglobinopathies (SITE) for the Management of Endocrine Complications in Patients with Haemoglobinopathies 84
Transfusional Approach in Multi-Ethnic Sickle Cell Patients: Real-World Practice Data From a Multicenter Survey in Italy 84
Reply to "Hepatocellular carcinoma in thalassemia and other hemoglobinopathies" 82
Prospective CMR Survey in Children With Thalassemia Major: Insights From a National Network 82
Thyroid Nodule Surveillance in Transfusion-Dependent Thalassemia: A Comparative Ultrasonographic Study 81
Nephrolithiasis in patients exposed to deferasirox and desferioxamine: probably an age-linked event with different effects on some renal parameters 81
Subarachnoid haemorrhage and cerebral vasculopathy in a child with sickle cell anaemia 81
Early splenectomy in sickle cell disease: another piece of the puzzle 80
Thalassemia-Associated mixed hypogonadism (TAMH): unraveling a unique endocrine pattern and its impact on cardiovascular risk 78
Prevalence and mortality trends of hemoglobinopathies in Italy: a nationwide study 78
Premature aging of the immune system affects the response to SARS-CoV-2 mRNA vaccine in β-thalassemia: role of an additional dose 77
Thalassaemia is paradoxically associated with a reduced risk of in-hospital complications and mortality in COVID-19: Data from an international registry 76
Mortality in β-thalassemia patients with confirmed pulmonary arterial hypertension on right heart catheterization 74
Long-term treatment with deferiprone enhances left ventricular ejection function when compared to deferoxamine in patients with thalassemia major 73
Impairment of Innate Immunity and Depletion of Vaccine‐Induced Memory B and T Cells in the Absence of the Spleen 68
Will the changing therapeutic landscape meet the needs of patients with sickle cell disease? 68
Limited access to transcranial Doppler screening and stroke prevention for children with sickle cell disease in Europe: Results of a multinational EuroBloodNet survey 67
Manual erythroexchange in sickle cell disease: multicenter validation of a protocol predictive of volume to exchange and hemoglobin values 67
Inflammatory and senescence-associated mediators affect the persistence of humoral response to COVID-19 mRNA vaccination in transfusion-dependent beta-thalassemic patients 64
Thalassemias and Sickle Cell Diseases in Pregnancy: SITE Good Practice 53
GROWTH ABNORMALITIES, ENDOCRINE, AND BONE DISEASE 45
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. 44
The phenotypes of sickle cell disease: strategies to aid the identification of undiagnosed patients in the Italian landscape 38
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 36
Incorporating national disease burden in GBD estimates of haemoglobinopathies in Italy 25
Corrigendum to "Characterisation of transfusion-dependent prediabetes using continuous glucose monitoring: The Haemoglycare study" [Diab. Res. Clin. Pract. 222 (2025) 112076] 20
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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 5
Totale 10.262
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Categoria #
all - tutte 33.947
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 33.947
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202183 0 0 0 0 0 0 0 0 0 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
2025/20265.956 234 283 332 303 556 3.327 272 269 237 143 0 0
Totale 10.265