IRIS
CASALE, Maddalena
 Distribuzione geografica
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Continente #
NA - Nord America 1.507
EU - Europa 1.464
AS - Asia 720
SA - Sud America 61
AF - Africa 6
Totale 3.758
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Nazione #
US - Stati Uniti d'America 1.498
IE - Irlanda 498
IT - Italia 380
SG - Singapore 332
HK - Hong Kong 218
GB - Regno Unito 146
DE - Germania 138
CN - Cina 119
UA - Ucraina 93
BR - Brasile 58
GR - Grecia 46
SE - Svezia 31
FR - Francia 30
FI - Finlandia 22
RU - Federazione Russa 22
TR - Turchia 19
AT - Austria 14
BE - Belgio 13
PK - Pakistan 10
CA - Canada 7
CH - Svizzera 7
NL - Olanda 7
CZ - Repubblica Ceca 4
IN - India 3
ID - Indonesia 2
JO - Giordania 2
KR - Corea 2
MK - Macedonia 2
MX - Messico 2
PT - Portogallo 2
RS - Serbia 2
UZ - Uzbekistan 2
AE - Emirati Arabi Uniti 1
AR - Argentina 1
BD - Bangladesh 1
BG - Bulgaria 1
CO - Colombia 1
CY - Cipro 1
DZ - Algeria 1
ET - Etiopia 1
HU - Ungheria 1
IQ - Iraq 1
IR - Iran 1
KE - Kenya 1
KZ - Kazakistan 1
LT - Lituania 1
LU - Lussemburgo 1
MA - Marocco 1
MD - Moldavia 1
PH - Filippine 1
PL - Polonia 1
PS - Palestinian Territory 1
RO - Romania 1
SC - Seychelles 1
TH - Thailandia 1
TW - Taiwan 1
VE - Venezuela 1
VN - Vietnam 1
ZA - Sudafrica 1
Totale 3.758
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Città #
Dublin 486
Santa Clara 287
Chandler 231
Hong Kong 218
Jacksonville 188
Singapore 97
Ann Arbor 88
Bremen 70
Princeton 70
Caserta 69
Roxbury 66
Medford 51
Beijing 43
Naples 39
New York 38
Woodbridge 35
Wilmington 25
Nanjing 24
Ercolano 23
Des Moines 22
Boardman 21
Ashburn 19
Cambridge 19
Grumo Nevano 17
Napoli 16
Brussels 13
Rome 13
Munich 12
Falkenstein 9
San Mateo 9
Helsinki 8
Pozzuoli 8
São Paulo 8
Milan 7
Nanchang 7
Nocera Inferiore 7
Nuremberg 7
Redwood City 7
Vienna 7
Fairfield 6
Mountain View 6
Elora 5
Istanbul 5
Kunming 5
Orlando 5
San Sebastiano al Vesuvio 5
Stella Cilento 5
Auburn Hills 4
Aversa 4
Brno 4
Changchun 4
Lappeenranta 4
Los Angeles 4
Pagani 4
Seattle 4
Shanghai 4
Tianjin 4
Belo Horizonte 3
Brasília 3
Casoria 3
Eboli 3
Florence 3
Gunzenhausen 3
Houston 3
Jinan 3
London 3
Norwalk 3
Rio Saliceto 3
Shenyang 3
Amman 2
Amsterdam 2
Bandung 2
Belgrade 2
Bitola 2
Caggiano 2
Campinas 2
Carpi 2
Den Haag 2
Dolo 2
Genoa 2
Lanzhou 2
Leawood 2
Lissone 2
Messina 2
Montes Claros 2
Mumbai 2
Newark 2
Oxford 2
Padova 2
Parma 2
Rimini 2
Salerno 2
San Giorgio A Cremano 2
Seoul 2
São José do Rio Preto 2
Tashkent 2
Algiers 1
Almaty 1
Altavilla Irpina 1
Angra dos Reis 1
Totale 2.560
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Nome #
Cognitive, Brain and Intracranial Artery Involvement in Beta Thalassemia 136
Effects of germline VHL deficiency on growth, metabolism, and mitochondria 102
HNF-1β mutation affects PKD2 and SOCS3 expression causing renal cysts and diabetes in MODY5 kindred. 101
Endocrine function and bone disease during long-term chelation therapy with deferasirox in patients with β-thalassemia major. 87
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation) 85
Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overload 82
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range. 78
National systematic approach to the management of asplenia: the set up of the Italian Network on Asplenia 73
Brain iron content in systemic iron overload: A beta-thalassemia quantitative MRI study 70
Asymptomatic intracranial aneurysms in beta-thalassemia: A three-year follow-up report 70
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 69
Congenital Dyserythropoietic Anemia Type II: molecular analysis and expression of the SEC23B Gene. 67
Long-term improvement in cardiac magnetic resonance in β-thalassemia major patients treated with deferasirox extends to patients with abnormal baseline cardiac function 65
A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil Deformity 65
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 65
Acute events in children with sickle cell disease in Italy during the COVID-19 pandemic: useful lessons learned 64
Splenectomy for hereditary spherocytosis: complete, partial or not at all? 61
Deferasirox: la chelazione ottimale nelle anemie trasfusione-dipendenti 61
Clinical outcome of transfusions with extended red blood cell matching in β-thalassemia patients: A single-center experience 61
Organizing national responses for rare blood disorders: The Italian experience with sickle cell disease in childhood 60
Predicting factors for liver iron overload at the first magnetic resonance in children with thalassaemia major 59
Long-term efficacy of deferasirox for cardiac siderosis in thalassemia major 57
Cb2 receptor stimulation and dexamethasone restore the anti-inflammatory and immune-regulatory properties of mesenchymal stromal cells of children with immune thrombocytopenia 56
Access to emergency department for acute events and identification of sickle cell disease in refugees. 56
Brain functional impairment in beta-thalassaemia: the cognitive profile in Italian neurologically asymptomatic adult patients in comparison to the reported literature 56
BONE MINERAL DENSITY IMPROVEMENT IN PATIENTS WITH THALASSEMIA MAJOR ON LONG-TERM CHELATION THERAPY WITH DEFERASIROX 55
Association between serum ferritin and liver iron concentration with cardiac iron in pediatric thalassemia major patients 55
Longitudinal Prospective MRI Study in Pediatric Patients With Thalassemia Major 55
Long term efficacy of iron chelation therapy with deferasirox on endocrine function in thalassemia major 54
An Educational Study Promoting the Delivery of Transcranial Doppler Ultrasound Screening in Paediatric Sickle Cell Disease: A European Multi-Centre Perspective 54
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: Analysis of 78 patients from 21 families 53
Iron chelating properties of Eltrombopag: Investigating its role in thalassemia-induced osteoporosis 53
No evidence of increased cerebrovascular involvement in adult neurologically-asymptomatic β-Thalassaemia. A multicentre multimodal magnetic resonance study 53
Italian patients with hemoglobinopathies exhibit a 5-fold increase in age-standardized lethality due to SARS-CoV-2 infection 53
Association of immune thrombocytopenia and celiac disease in children: A retrospective case control study 52
Extramedullary haematopoiesis correlates with genotype and absence of cardiac iron overload in polytransfused adults with thalassaemia 50
Multiparametric Cardiac Magnetic Resonance Survey in Children With Thalassemia Major: A Multicenter Study 49
Life-Threatening Drug-Induced Liver Injury in a Patient with β-Thalassemia Major and Severe Iron Overload on Polypharmacy. 49
Hydroxyurea prescription, availability and use for children with sickle cell disease in Italy: Results of a National Multicenter survey. 48
Red blood cell alloimmunisation in transfusion-dependent thalassaemia: A systematic review 48
Rubrica a cura di luciano de seta quando il saturimetro mente… 48
Second-line therapy in paediatric warm autoimmune haemolytic anaemia. Guidelines from the Associazione Italiana Onco-Ematologia Pediatrica (AIEOP) 47
Headache in beta-thalassemia: An Italian multicenter clinical, conventional MRI and MR-angiography case-control study 47
Nephrolithiasis in patients exposed to deferasirox and desferioxamine: probably an age-linked event with different effects on some renal parameters 45
Clinical and molecular spectrum of glucose-6-phosphate isomerase deficiency. Report of 12 new cases 44
Tricuspid-valve regurgitant jet velocity as a risk factor for death in β-Thalassemia. 42
Prospective MRI study in pediatric thalassemia major (TM) patients in the MIOT network: a tool to strengthen medical decisions 41
Effect of splenectomy on iron balance in patients with β-thalassemia major: a long-term follow-up 40
Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene 40
Hb Vanvitelli: A new unstable α-globin chain variant causes undiagnosed chronic haemolytic anaemia when co-inherited with deletion − α3.7. 40
Myocardial fibrosis by CMR LGE in a large cohort of pediatric thalassemia major patients 39
Subarachnoid haemorrhage and cerebral vasculopathy in a child with sickle cell anaemia 38
White matter volume changes in adult beta-thalassemia: Negligible and unrelated to anemia and cognitive performances 38
Nineteen-month-old girl with persistent fever 37
Current challenges in the management of patients with sickle cell disease - A report of the Italian experience 37
Management of the risk for severe infections in children with asplenia: Recommendations from the Italian Network of Asplenia 37
Good Clinical Practice of the Italian Society of Thalassemia and Haemoglobinopathies (SITE) for the Management of Endocrine Complications in Patients with Haemoglobinopathies 37
Long-term treatment with deferiprone enhances left ventricular ejection function when compared to deferoxamine in patients with thalassemia major 36
HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype-phenotype correlation 36
No increased cerebrovascular involvement in adult beta-thalassemia by advanced MRI analyses 35
Disease burden and quality of life of in children with sickle cell disease in Italy: time to be considered a priority 35
Transfusional Approach in Multi-Ethnic Sickle Cell Patients: Real-World Practice Data From a Multicenter Survey in Italy 35
[The Management of Endocrine Complications in Patients with Haemoglobinopathies: Good Clinical Practice of the Italian Society of Thalassemia and Haemoglobinopathies (SITE).] 32
Mortality in β-thalassemia patients with confirmed pulmonary arterial hypertension on right heart catheterization 30
Childhood Multiple Endocrine Neoplasia (MEN) Syndromes: Genetics, Clinical Heterogeneity and Modifying Genes 27
Will the changing therapeutic landscape meet the needs of patients with sickle cell disease? 27
Juvenile erythrocytosis in children after liver transplantation: prevalence, risk factors and outcome 27
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 26
Prospective CMR Survey in Children With Thalassemia Major: Insights From a National Network 26
Manual erythroexchange in sickle cell disease: multicenter validation of a protocol predictive of volume to exchange and hemoglobin values 26
Response to measles, mumps and rubella (Mmr) vaccine in transfusion-dependent patients 26
Selecting β-thalassemia Patients for Gene Therapy: A Decision-making Algorithm 26
Incidence of cancer and related deaths in hemoglobinopathies: A follow-up of 4631 patients between 1970 and 2021 25
Thalassaemia is paradoxically associated with a reduced risk of in-hospital complications and mortality in COVID-19: Data from an international registry 25
Premature aging of the immune system affects the response to SARS-CoV-2 mRNA vaccine in β-thalassemia: role of an additional dose 24
Recommendations for the management of acute immune thrombocytopenia in children. A Consensus Conference from the Italian Association of Pediatric Hematology and Oncology 22
Long‐term outcomes of avascular necrosis in sickle cell disease using joint‐specific patient‐reported outcome measures: Results from a multicentre study 19
Reply to "Hepatocellular carcinoma in thalassemia and other hemoglobinopathies" 19
Inflammatory and senescence-associated mediators affect the persistence of humoral response to COVID-19 mRNA vaccination in transfusion-dependent beta-thalassemic patients 19
Transient erythroblastopenia of childhood after COVID-19 infection: a case report 18
Early splenectomy in sickle cell disease: another piece of the puzzle 13
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 12
Limited access to transcranial Doppler screening and stroke prevention for children with sickle cell disease in Europe: Results of a multinational EuroBloodNet survey 10
Impairment of Innate Immunity and Depletion of Vaccine‐Induced Memory B and T Cells in the Absence of the Spleen 6
Screening for sickle cell disease by point-of-care tests in Italy: pilot study on 1000 at risk children 6
Prevalence and mortality trends of hemoglobinopathies in Italy: a nationwide study 5
Characterisation of transfusion-dependent prediabetes using continuous glucose monitoring: The Haemoglycare study 4
Thalassemias and Sickle Cell Diseases in Pregnancy: SITE Good Practice 2
Totale 3.963
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Categoria #
all - tutte 20.347
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 20.347
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020114 0 0 0 0 0 0 0 0 47 12 47 8
2020/2021290 17 5 20 34 33 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
2024/20251.086 10 10 10 44 212 163 244 170 223 0 0 0
Totale 3.963