COLOMBATTI, RAFFAELLA
 Distribuzione geografica
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Continente #
NA - Nord America 3.855
EU - Europa 347
AS - Asia 157
AF - Africa 8
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 4.369
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Nazione #
US - Stati Uniti d'America 3.845
IT - Italia 137
CN - Cina 101
FI - Finlandia 64
SE - Svezia 55
VN - Vietnam 36
DE - Germania 35
GB - Regno Unito 32
UA - Ucraina 13
CA - Canada 9
IE - Irlanda 6
IR - Iran 5
CM - Camerun 4
CY - Cipro 3
EG - Egitto 3
HK - Hong Kong 3
IN - India 3
IQ - Iraq 2
NL - Olanda 2
TR - Turchia 2
AU - Australia 1
EU - Europa 1
GR - Grecia 1
JM - Giamaica 1
JP - Giappone 1
PH - Filippine 1
PL - Polonia 1
RO - Romania 1
TZ - Tanzania 1
Totale 4.369
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Città #
Fairfield 740
Woodbridge 459
Houston 353
Chandler 334
Ashburn 299
Seattle 275
Cambridge 250
Wilmington 236
Ann Arbor 176
Princeton 85
Medford 67
San Diego 65
Jacksonville 63
Padova 48
Des Moines 46
Beijing 40
Roxbury 37
Dong Ket 36
Helsinki 35
Nanjing 18
Boardman 17
Milan 17
London 12
New York 12
North York 8
Norwalk 7
Dublin 6
Shenyang 6
Guangzhou 5
Nanchang 5
Villaga 5
Washington 5
Changsha 4
Hebei 4
Tianjin 4
Borås 3
Chicago 3
Hong Kong 3
Kilburn 3
Lappeenranta 3
Nicosia 3
Ogden 3
Rome 3
Silver Spring 3
Ardabil 2
Busto Arsizio 2
Charlotte 2
Douala 2
Jiaxing 2
Jinan 2
Karaj 2
Kunming 2
Las Vegas 2
Margherita Di Savoia 2
Modena 2
Monselice 2
Noventa di Piave 2
Scuola 2
Southwark 2
St Louis 2
Yenibosna 2
Ancona 1
Bologna 1
Chengdu 1
Chiswick 1
Costa Mesa 1
Council Bluffs 1
Danbury 1
Dar es Salaam 1
Dartford 1
Edinburgh 1
Frankfurt am Main 1
Geislingen an der Steige 1
Genoa 1
Gurgaon 1
Hefei 1
Hounslow 1
Indiana 1
Islington 1
Kingston 1
New Bedfont 1
Philadelphia 1
Phoenix 1
Poughkeepsie 1
Prescot 1
Redwood City 1
Rochester 1
Rosà 1
San Francisco 1
San Mateo 1
Serravalle Scrivia 1
Shanghai 1
Tokyo 1
Torino 1
Treviso 1
Verona 1
Vicenza 1
Vigodarzere 1
Wandsworth 1
Yellow Springs 1
Totale 3.879
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Nome #
Spleen histology in children with sickle cell disease and hereditary spherocytosis: Hints on the disease pathophysiology 137
Pulmonary hypertension in sickle cell disease children under 10 years of age 129
Malaria prevention reduces in-hospital mortality among severely ill tuberculosis patients: a three-step intervention in Bissau, Guinea-Bissau. 121
Transcranial Doppler Sonography in children with sickle cell disease and silent ischemic lesions 119
Treosulfan-based conditioning regimen in sibling and alternative donor hematopoietic stem cell transplantation for children with sickle cell disease 115
Hospitalization of children with sickle cell disease in a region with increasing immigration rates. 110
Cognitive evoked potentials and neural networks are abnormal in children with sickle cell disease and not related to the degree of anaemia, pain and silent infarcts 110
Results of a multicenter universal newborn screening program for sickle cell disease in Italy: A call to action 109
European Intergroup Studies (MMT4-89 and MMT4-91) on Childhood Metastatic Rhabdomyosarcoma: Final Results and Analysis of Prognostic Factors 108
Coagulation Activation in Children with Sickle Cell Disease Is Associated with Cerebral Small Vessel Vasculopathy 105
Airways obstruction and pulmonary capillary blood volume in children with sickle cell disease 105
Tricuspid regurgitant velocity elevation in a three-year old child with sickle cell anemia and recurrent acute chest syndromes reversed not by hydroxyurea but by bone marrow transplantation 103
Intellectual impairment and TCD evaluation in children with sickle cell disease and silent stroke 102
Haploidentical stem cell transplantation cures autoimmune hepatitis and cerebrovascular disease in a patient with sickle cell disease 97
Comprehensive care for sickle cell disease immigrant patients: A reproducible model achieving high adherence to minimum standards of care. 96
Visual cortex changes in children with sickle cell disease and normal visual acuity: a multimodal magnetic resonance imaging study 95
Evaluation of Technical Issues in a Pilot Multicenter Newborn Screening Program for Sickle Cell Disease 92
Newborn screening for sickle cell disease in Europe: recommendations from a Pan-European Consensus Conference 86
Acute Chest Syndrome in Children with Sickle Cell Disease in Italy: Results of a National Survey from the Italian Association of Pediatric Hematology Oncology (AIEOP) 80
A study of the geographic distribution and associated risk factors of leg ulcers within an international cohort of sickle cell disease patients: the CASiRe group analysis 78
primary stroke prevention for sickle cell disease in north-east Italy: the role of ethnic issues in establishing a Transcranial Doppler screening program 77
Hydroxyurea prescription, availability and use for children with sickle cell disease in Italy: Results of a National Multicenter survey 77
Intellectual function evaluation of first generation immigrant children with sickle cell disease: the role of language and sociodemographic factors 76
INTENSIVE CHEMOTHERAPY FOR CHILDREN AND YOUNG ADULTS WITH METASTATIC NEUROECTODERMAL TUMORS OF THE SOFT TISSUE 75
Longitudinal evaluation of cerebral white matter hyperintensities lesion volume in children with sickle cell disease 74
Selective Difficulties in Lexical Retrieval and Nonverbal Executive Functioning in Children With HbSS Sickle Cell Disease 73
High-dose melphalan with autologous stem-cell rescue in metastatic rhabdomyosarcoma 64
Microvasculopathy and biomarkers in sickle cell disease: the promise of non-invasive real-time in vivo tools 63
Anemia and transfusion in the neonate 63
A multinational trial of prasugrel for sickle cell vaso-occlusive events 62
Childhood sickle cell disease in north-east Italy: genetic, hematologic, clinical characteristics and social challenges of an emerging disease: a single center experience 57
An Analysis of Racial and Ethnic Backgrounds Within the CASiRe International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical Research 55
Association between a combination of single nucleotide polymorphisms and large vessel cerebral vasculopathy in African children with sickle cell disease 55
The Management of Sickle Cell Pain in the Emergency Department: A Priority For Health Systems. 54
ENERCA clinical recommendations for disease management and prevention of complications of sickle cell disease in children 54
Newborn screening for sickle cell disease in Europe 50
An Educational Study Promoting the Delivery of Transcranial Doppler Ultrasound Screening in Paediatric Sickle Cell Disease: A European Multi-Centre Perspective 48
Lipoarabinomannan antigenic epitope differences in tuberculosis disease subtypes 47
Thrombocytopenia and splenomegaly: An unusual presentation of congenital hepatic fibrosis 44
Feasibility and effectiveness of tuberculosis active case-finding among children living with tuberculosis relatives: A cross-sectional study in Guinea-Bissau 41
Direct detection by the xpert MTB/RIF assay and characterization of multi and poly drug- resistant tuberculosis in Guinea-Bissau, West Africa 41
Cognition and the default mode network in children with sickle cell disease: A resting state functional MRI study 40
A short-term intervention for the treatment of severe malnutrition in a post-conflict country: Results of a survey in Guinea Bissau 40
Age of first pain crisis and associated complications in the CASiRe international sickle cell disease cohort 40
Paediatric Emergency Department use and risk factors for admission in Sickle Cell Disease Children in a country without comprehensive care 40
Problematiche acute dell’Anemia Falciforme nel bambino: esperienza del Pronto Soccorso Pediatrico di Padova 39
Dalla Guinea Bissau a Padova per l’alta specializzazione:un nuovo modello per la globalozzazione della Pediatria? 37
Monitoring oral iron therapy in children with iron deficiency anemia: an observational, prospective, multicenter study of AIEOP patients (Associazione Italiana Emato-Oncologia Pediatrica) 37
Geographic Differences in Phenotype and Treatment of Children with Sickle Cell Anemia from the Multinational DOVE Study 37
Organizing national responses for rare blood disorders: The Italian experience with sickle cell disease in childhood 37
Successful Treatment of Severe Iatrogenic Calcinosis Cutis with Intravenous Sodium Thiosulfate in a Child Affected by T-Acute Lymphoblastic Leukemia 36
Lessons learned from the H1N1 pandemic: The need to improve systematic vaccination in Sickle Cell Disease children. A multi center survey in Italy 36
The Guinea-Bissau Family of Mycobacterium tuberculosis Complex Revisited 35
Recombinant erythropoietin vs. blood transfusion care in infants with hereditary spherocytosis: a retrospective cohort study of A.I.E.O.P. patients (Associazione Italiana Emato-Oncologia Pediatrica) 35
Impact of sickle cell disease on patients' daily lives, symptoms reported, and disease management strategies: Results from the international Sickle Cell World Assessment Survey (SWAY) 34
Editorial for special issue “newborn screening for sickle cell disease and other haemoglobinopathies” 32
Complicanze acute dell’anemia falciforme nel bambino: progressi nell’ottimizzazione delle cure ed aree suscettibili di miglioramento nell’esperienza del Pronto Soccorso Pediatrico di Padova 31
Intracranial circulation in sickle cell disease 30
THE ROLE OF EXECUTIVE DYSFUNCTIONS IN THE VERBAL LANGUAGE DEFICITS OF CHILDREN WITH SICKLE CELL DISEASE 30
Treatment of dental and orthodontic complications in thalassaemia 30
Annual Academy of Sickle Cell and Thalassaemia (ASCAT) conference: a summary of the proceedings 30
Crisi dolorose articolari in bambini di colore: il sospetto di anemia falciforme nel Pronto Soccorso pediatrico di un’area non endemica 29
HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype-phenotype correlation 29
Novel findings from the multinational DOVE study on geographic and age-related differences in pain perception and analgesic usage in children with sickle cell anaemia 29
Current challenges in the management of patients with sickle cell disease - A report of the Italian experience 29
European migration crises: The role of national hemoglobinopathy registries in improving patient access to care 25
Short term advantages of a public-private partnership for tuberculosis in Guinea Bissau: Reduction of mortality and increased diagnostic capacity 23
Distribution of HbS Allele and Haplotypes in a Multi-Ethnic Population of Guinea Bissau, West Africa: Implications for Public Health Screening 23
Contamination of drinking water sources during the rainy season in an urban post-conflict community in Guinea Bissau: implications for sanitation priority 21
Real-Life experience with hydroxyurea in patients with sickle cell disease: Results from the prospective ESCORT-HU cohort study 19
American Society of Hematology 2020 Podcast Collection: Sickle Cell Anaemia 15
Disease burden and quality of life of in children with sickle cell disease in Italy: time to be considered a priority 15
Acute events in children with sickle cell disease in Italy during the COVID-19 pandemic: useful lessons learned 14
Erythrocyte microRNAs: a tiny magic bullet with great potential for sickle cell disease therapy 14
The impact of Parvovirus B19 on hereditary haemolytic anaemias 14
Pediatric Moyamoya Disease and Syndrome in Italy: A Multicenter Cohort 13
Severe hemolytic anemia in a newborn: Look out for rare Gardos channelopathies due to KCNN4 mutation 12
Global geographic differences in healthcare utilization for sickle cell disease pain crises in the CASiRe cohort 9
Health-related quality of life in hemoglobinopathies: A systematic review from a global perspective 8
Pain Frequency and Health Care Utilization Patterns in Women with Sickle Cell Disease Experiencing Menstruation-Associated Pain Crises 6
CK2β Regulates Hematopoietic Stem Cell Biology and Erythropoiesis 6
Challenges and Opportunities of Precision Medicine in Sickle Cell Disease: Novel European Approach by GenoMed4All Consortium and ERN-EuroBloodNet 6
Standardizing elements of care in pediatric sickle cell disease centers: The road toward health equity 5
Treatment of dental and orthodontic complications in thalassaemia 5
Point-of-care testing allows successful simultaneous screening of sickle cell disease, HIV, and tuberculosis for households in rural Guinea-Bissau, West Africa 5
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 5
Environmental Factors in Northern Italy and Sickle Cell Disease Acute Complications: A Multicentric Study 5
Pain Burden in the CASiRe International Cohort of Sickle Cell Patients: United States and Ghana 5
Defining global strategies to improve outcomes in sickle cell disease: a Lancet Haematology Commission 4
Sickle cell disease landscape and challenges in the EU: the ERN-EuroBloodNet perspective 4
Relationship between hemoglobin, hemolysis, and transcranial Doppler velocities in children with sickle cell disease: Results from a long-term natural history study in Italy in the era of multimodal therapy 4
Author Correction: Lipoarabinomannan antigenic epitope differences in tuberculosis disease subtypes 3
The family pediatrician and the shared management of children with hemato-oncological diseases|Il pediatra di famiglia e la gestione condivisa tra ospedale e territorio del bambino emato-oncologico 2
Transfusional Approach in Multi-Ethnic Sickle Cell Patients: Real-World Practice Data From a Multicenter Survey in Italy 2
Hematological characteristics and hepatobiliary complications of hereditary spherocytosis in a tertiary care pediatric center: optimizing diagnosis and care through local and international networks 2
Sickle cell disease: embedding patient participation into an international conference can transform the role of lived experience 1
Systematic Literature Review Shows Gaps in Data on Global Prevalence and Birth Prevalence of Sickle Cell Disease and Sickle Cell Trait: Call for Action to Scale Up and Harmonize Data Collection 1
Prevention of neurovascular complications in children with Sickle Cell Disease in the real-world setting: What adult medicine physicians should know 1
A Phase 3 Randomized Trial of Voxelotor in Sickle Cell Disease 1
Haemochromatosis in children: A national retrospective cohort promoted by the A.I.E.O.P. (Associazione Italiana Emato‐Oncologia Pediatrica) study group 1
Totale 4.468
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Categoria #
all - tutte 19.631
article - articoli 19.502
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 39.133
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019211 0 0 0 0 0 0 0 0 0 42 93 76
2019/2020511 73 16 7 34 47 48 49 66 72 46 34 19
2020/20211.419 23 19 31 406 10 176 135 120 174 146 60 119
2021/2022942 22 37 102 63 79 81 25 149 69 29 77 209
2022/2023663 177 73 13 73 83 56 5 48 74 2 54 5
2023/2024313 20 54 47 32 25 43 25 37 21 9 0 0
Totale 4.469