IRIS
CANZONIERI, CECILIA
 Distribuzione geografica
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Continente #
NA - Nord America 442
EU - Europa 324
AS - Asia 283
AF - Africa 3
SA - Sud America 2
OC - Oceania 1
Totale 1.055
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Nazione #
US - Stati Uniti d'America 441
CN - Cina 241
IE - Irlanda 132
FI - Finlandia 52
UA - Ucraina 48
SG - Singapore 36
IT - Italia 27
DE - Germania 26
SE - Svezia 15
GB - Regno Unito 13
FR - Francia 8
MU - Mauritius 3
IN - India 2
PK - Pakistan 2
AU - Australia 1
AZ - Azerbaigian 1
BE - Belgio 1
BO - Bolivia 1
CA - Canada 1
JP - Giappone 1
LU - Lussemburgo 1
NL - Olanda 1
PE - Perù 1
Totale 1.055
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Città #
Dublin 132
Chandler 115
Jacksonville 63
Nanjing 63
Singapore 33
Ashburn 32
Beijing 32
Boardman 29
Nanchang 23
Helsinki 21
Changsha 19
Lawrence 18
Medford 18
Princeton 18
Shenyang 18
Hebei 16
Shanghai 16
Seattle 15
Jiaxing 13
Wilmington 13
Tianjin 11
Ann Arbor 10
Pavia 10
Woodbridge 8
Hangzhou 7
Des Moines 5
Milan 5
New York 5
Goito 3
Norwalk 3
Fairfield 2
Houston 2
Jinan 2
Los Angeles 2
Pune 2
Sargodha 2
Taizhou 2
Tappahannock 2
Auburn Hills 1
Baku 1
Borås 1
Brussels 1
Cedar Knolls 1
Changchun 1
Chicago 1
Chongqing 1
Genova 1
Kunming 1
La Paz 1
Lana 1
Lanzhou 1
Lima 1
Luxembourg 1
Ningbo 1
Pisa 1
Ponte San Pietro 1
Shijiazhuang 1
Stockholm 1
Tangshan 1
Tokyo 1
Toronto 1
Xingtai 1
Zhengzhou 1
Totale 815
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Nome #
Bioinformatic Analysis of Pathogenic Missense Mutationsof Activin Receptor Like Kinase 1 Ectodomain 87
Increase of circulating endothelial cells in patients with Hereditary Hemorrhagic Telangiectasia. 75
Immunohistochemical analysis of a merkeloma observed in a patient affected byhereditary haemorrhagic telangiectasia. 71
Rendu-Osler-Weber patients have an increasd frequency of mature endothelial cells in peripheral blood 68
STRUCTURAL MODELLING OF ALK1 ECTO-DOMAIN 66
Breast cancer and genetics 63
Hereditary Hemorrhagic Telangiectasia: Breakpoint Characterization of a Novel Large Deletion in ACVRL1 Suggests the Causing Mechanism. 62
Bioinformatics as a Starting Point for the Analysis of ALK1 Missense Mutations 62
Natural history and outcome of hepatic ascular malformations in a large cohort of patients with hereditary hemorrhagic teleangiectasia 59
Endoscopic evaluation of gastrointestinal tract in patients with hereditary hemorrhagic telangiectasia and correlation with their genotypes. 57
Pulmonary artery systolic pressure as estimated by TTE in a group of HHT patients. 57
Efficacy of thalidomide in the treatment of severe recurrent epistaxis in hereditary hemorrhagic teleangiectasia: a comparison between HHT1 and 2. 56
Hereditary haemorrhagic telangiectasia in North African and sub-Saharan patients. 53
Canzonieri Cecilia; Ornati Federica; Matti Elina; Chu Francesco; Manfredi Guido; Olivieri Carla; Buscarini Elisabetta; Pagella Fabio; Cesare Danesino. 50
“The Italian Job”: our experience in HHT management 50
Argon plasma coagulation is an effective treatment for hereditary hemorrhagic telangiectasia patients with severe nosebleeds. 50
Estimated Pulmonary Artery Systolic Pressure In A Group Of 105 HHT Patients Discloses Differences In Patients Carrying Acvrl1 or Eng Mutations. 46
Modelling of ALK1 ectodomain and ALK1-ActRIIA-BMP9 receptor complex: hints from Type 2 Hereditary Haemorrhagic Telangiectasia 40
Totale 1.072
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Categoria #
all - tutte 4.422
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 4.422
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202061 0 0 0 0 0 10 2 11 16 17 4 1
2020/202195 13 9 4 13 3 11 1 14 2 12 11 2
2021/202273 0 1 0 1 1 0 0 8 6 4 10 42
2022/2023322 28 37 4 19 34 31 0 13 145 1 9 1
2023/2024125 22 14 1 7 4 24 2 39 2 4 3 3
2024/202576 5 18 14 10 21 8 0 0 0 0 0 0
Totale 1.072