IRIS
MELAZZINI, FEDERICA
 Distribuzione geografica
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Continente #
NA - Nord America 1.029
EU - Europa 774
AS - Asia 513
OC - Oceania 3
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
SA - Sud America 1
Totale 2.322
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Nazione #
US - Stati Uniti d'America 1.010
CN - Cina 455
IE - Irlanda 322
IT - Italia 227
FI - Finlandia 84
DE - Germania 35
SG - Singapore 24
IN - India 20
CA - Canada 19
UA - Ucraina 19
SE - Svezia 18
GB - Regno Unito 14
RO - Romania 14
BE - Belgio 9
RU - Federazione Russa 9
CH - Svizzera 8
IR - Iran 5
JP - Giappone 5
CZ - Repubblica Ceca 4
FR - Francia 4
AU - Australia 3
GR - Grecia 2
IL - Israele 2
PT - Portogallo 2
RS - Serbia 2
BD - Bangladesh 1
CL - Cile 1
DK - Danimarca 1
EG - Egitto 1
EU - Europa 1
ID - Indonesia 1
Totale 2.322
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Città #
Dublin 322
Chandler 256
Nanjing 100
Ashburn 91
Beijing 84
Boardman 68
Jacksonville 64
Helsinki 54
Milan 53
Princeton 51
Lawrence 47
New York 46
Medford 43
Wilmington 43
Changsha 40
Shanghai 40
Hebei 35
Pavia 32
Nanchang 31
Shenyang 29
Jiaxing 22
Pune 20
Ann Arbor 18
Hangzhou 18
Tianjin 17
Singapore 14
Toronto 14
Guangzhou 12
Los Angeles 10
Norwalk 10
Timisoara 10
Brussels 9
Rome 9
Fairfield 7
Seattle 7
Palermo 6
Woodbridge 6
Zurich 6
Brescia 5
Caccamo 5
Falls Church 5
Rozzano 5
Tokyo 5
Zhengzhou 5
Cagliari 4
Turin 4
Andover 3
Bari 3
Brno 3
Chongqing 3
Desio 3
Jinan 3
Laives 3
Moscow 3
Paceco 3
Redwood City 3
Tehran 3
Verona 3
Auburn Hills 2
Bad Sobernheim 2
Belgrade 2
Borgomanero 2
Corsico 2
Dallas 2
Florence 2
Foligno 2
Geneva 2
Houston 2
Liscate 2
Marcignago 2
Mariglianella 2
Martinengo 2
Ottawa 2
Pieve Emanuele 2
Piscataway 2
Porto 2
Ramat Gan 2
Rho 2
Rockville 2
Sacramento 2
Santa Clara 2
Siziano 2
Taizhou 2
Tolentino 2
Torino 2
Venegono Superiore 2
Washington 2
Borås 1
Böblingen 1
Cairo 1
Casier 1
Castelraimondo 1
Chicago 1
Como 1
Costa Masnaga 1
Des Moines 1
Edmonton 1
Falkenstein 1
Fayetteville 1
Frankfurt Am Main 1
Totale 1.889
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Nome #
Impaired respiratory function reduces haemoglobin oxygen affinity in COVID-19 119
Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders. 78
Analysis of 65 pregnancies in 34 women with five different forms of inherited platelet function disorders 67
Clinical and pathogenetic characterization of ETV6-related thrombocytopenia (ETV6-RT), an inherited thrombocytopenia (IT) predisposing to childhood acute lymphoblastic leukemia (ALL) 66
Personalized reference intervals for platelet count reduce the number of subjects with unexplained thrombocytopenia 60
NOVEL PERSPECTIVES IN GENOTYPE-PHENOTYPE CORRELATIONS IN MYH9-RELATED DISEASE: NO LONGER JUST A MATTER OF HEAD OR TAIL 60
Correction to: Anemia in patients with Covid-19: pathogenesis and clinical significance (Clinical and Experimental Medicine, (2021), 10.1007/s10238-020-00679-4) 60
Platelet size distinguishes between inherited macrothrombocytopenias and immune thrombocytopenia. 58
Depletion of circulating IgM memory B cells predicts unfavourable outcome in COVID-19 58
Bleeding risk of surgery and its prevention in patients with inherited platelet disorders. The Surgery in Platelet disorders And Therapeutic Approach (SPATA) study 57
A MONOALLELIC LOSS-FUNCTION MUTATION IN THE THROMBOPOIETIN (THPO) GENE IS RESPONSIBLE FOR A NEW FORM OF INHERITED THROMBOCYTOPENIA (IT) 57
Impact of COVID-19 on liver function: results from an internal medicine unit in Northern Italy 56
5′UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia 55
Bleeding is not the main clinical issue in many patients with inherited thrombocytopaenias 54
ETV6-RELATED THROMBOCYTOPENIA (ETV6-RT): CLINICAL AND PATHOGENETIC CHARACTERIZATION OF AN INHERITED THROMBOCYTOPENIA (IT) PREDISPOSING TO CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA (ALL) 54
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIb{alpha} (Bolzano mutation). 53
Platelet size for distinguishing between inherited thrombocytopenias and immune thrombocytopenia: a multicentric, real life study 52
Clinical and genetic aspects Bernard-Soulier syndrome: searching for genotype/phenotype correlations. 52
Diagnostic Delay of Pulmonary Embolism in COVID-19 Patients 52
NOVEL RUNX1 MUTATIONS IN FAMILIES WITH INHERITED THROMBOCYTOPENIA 51
Massive mediastinal enlargement due to extramedullary haematopoiesis in a patient with MYH9-related thrombocytopenia 51
A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene 50
Inherited thrombocytopenias—recent advances in clinical and molecular aspects 49
Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy 49
COMBINING NEXT GENERATION SEQUENCING WITH CLINICAL STUDIES TO UNRAVEL NOVEL INHERITED THROMBOCYTOPENIAS AFFECTING HALF OF THE PATIENTS 47
Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations 46
Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations. 45
Letter: Safety and efficacy issues of tirofiban use in endovascular procedures: What are the actual indications? 45
Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemia 45
ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia 45
QTc prolongation and mortality in SARS-2-CoV-infected patients treated with azithromycin and hydroxychloroquine 45
Mutations of RUNX1 in families with inherited thrombocytopenia 44
Correction to: Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy (Internal and Emergency Medicine, (2021), 16, 5, (1141-1152), 10.1007/s11739-020-02550-6) 43
Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim 42
Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy 41
Personalized reference intervals for platelet count reduce the number of subjects with unexplained thrombocytopenia 40
COVID-19-related symptom clustering in a primary care vs internal medicine setting 40
Seronegative autoimmune diseases: A challenging diagnosis 39
Dysregulation of oncogenic factors by GFI1B p32: investigation of a novel GFI1B germline mutation 39
Anemia in patients with Covid-19: pathogenesis and clinical significance 37
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families. 35
New roles for mean platelet volume measurement in the clinical practice? 33
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC 33
Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk disorders. In patients the SPATA-DVT with inherited Study platelet 33
Extramedullary hematopoiesis: a new feature of inherited thrombocytopenias? 30
Platelets in Thrombotic and Non-Thrombotic Disorders Pathophysiology, Pharmacology and Therapeutics: an Update 29
Research at the heart of hematology: Thrombocytopenias and platelet function disorders 29
Corrigendum: Diagnostic Delay of Pulmonary Embolism in COVID-19 Patients 28
The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology 26
A mid-term follow-up with a lung ultrasonographic score correlates with the severity of COVID-19 acute phase 24
QTc prolongation and mortality in SARS-2-CoV-infected patients treated with azithromycin and hydroxychloroquine 20
Venous thromboembolism in chronic gastrointestinal disorders 20
Determinants of COVID-19-related mortality in an internal medicine setting 19
Peptic Ulcer Disease as a Common Cause of Bleeding in Patients with Coronavirus Disease 2019 14
Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup 11
Totale 2.485
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Categoria #
all - tutte 11.175
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 11.175
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020288 0 184 1 3 1 6 2 4 5 29 47 6
2020/2021126 6 16 3 4 4 8 3 24 23 13 20 2
2021/2022261 7 1 28 1 9 6 3 10 12 13 35 136
2022/2023774 69 67 11 56 60 64 0 31 359 9 33 15
2023/2024557 46 61 12 26 107 129 33 37 7 38 24 37
2024/2025105 36 69 0 0 0 0 0 0 0 0 0 0
Totale 2.485