Pugnaloni, Flaminia
 Distribuzione geografica
Continente #
NA - Nord America 258
EU - Europa 151
AS - Asia 63
AF - Africa 2
SA - Sud America 1
Totale 475
Nazione #
US - Stati Uniti d'America 256
IT - Italia 85
SG - Singapore 30
SE - Svezia 20
IN - India 17
FI - Finlandia 11
BG - Bulgaria 8
CN - Cina 7
DE - Germania 5
ID - Indonesia 5
CH - Svizzera 4
IE - Irlanda 4
NL - Olanda 4
GB - Regno Unito 3
IR - Iran 3
LU - Lussemburgo 3
CA - Canada 2
RO - Romania 2
UA - Ucraina 2
EC - Ecuador 1
IL - Israele 1
MU - Mauritius 1
TG - Togo 1
Totale 475
Città #
Chandler 43
Fairfield 32
Rome 31
Ashburn 18
Singapore 18
Houston 14
Woodbridge 13
Cambridge 12
Helsinki 11
Wilmington 11
Seattle 10
Sofia 8
Pescara 7
Princeton 7
Hyderabad 6
San Paolo di Civitate 6
Campobasso 5
Jakarta 5
Ann Arbor 4
Changsha 4
Dublin 4
Lawrence 4
Milan 4
Andover 3
Bern 3
Boardman 3
Boston 3
Los Angeles 3
Luxembourg 3
Millbury 3
Beijing 2
Campofelice Di Roccella 2
Dearborn 2
Forlì 2
Naples 2
New York 2
Norwalk 2
Plano 2
Santa Clara 2
Velp 2
Ardea 1
Azor 1
Bengaluru 1
Bologna 1
Bonn 1
Bucharest 1
Des Moines 1
Falkenstein 1
Falls Church 1
Fondi 1
Guangzhou 1
Kilburn 1
Lomé 1
Manchester 1
Marano di Napoli 1
Montréal 1
Newark 1
Nieuwegein 1
Phoenix 1
Portici 1
Pune 1
Quito 1
San Diego 1
Toronto 1
Trumbull 1
Udine 1
Velletri 1
Wandsworth 1
Washington 1
Zurich 1
Totale 348
Nome #
Atrioventricular canal defect and genetic syndromes: the unifying role of sonic hedgehog 86
Atrioventricular canal defect is the classic congenital heart disease in Bardet-Biedl syndrome 64
A dangerous food binge. a case report of hypokalemic periodic paralysis and review of current literature 54
Cardiac defects and genetic syndromes: old uncertainties and new insights 51
null 49
Genetics of atrioventricular canal defects 45
Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study 30
Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease 24
22q11.2 Deletion Syndrome. Impact of Genetics in the Treatment of Conotruncal Heart Defects 23
Coexisting genetic findings in a cohort of patients with laboratory confirmation of 22q11.2 deletion syndrome 21
Crossed pulmonary arteries: An underestimated cardiovascular variant with a strong association with genetic syndromes{\textemdash}A report of 74 cases with systematic review of the literature 21
Some Isolated Cardiac Malformations Can Be Related to Laterality Defects 17
null 13
Smith–Magenis syndrome: Report of morphological and new functional cardiac findings with review of the literature 6
CA125: a novel cardiac biomarker for infants with congenital diaphragmatic hernia 5
Early Postnatal Ventricular Disproportion Predicts Outcome in Congenital Diaphragmatic Hernia 3
Staphylococcal Infections and Neonatal Skin: Data from Literature and Suggestions for the Clinical Management from Four Challenging Patients 3
Echocardiographic Assessment of Pulmonary Hypertension in Neonates with Congenital Diaphragmatic Hernia Using Pulmonary Artery Flow Characteristics 2
Totale 517
Categoria #
all - tutte 2.276
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 2.276


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202032 0 0 0 0 4 6 5 5 6 3 3 0
2020/202145 3 0 2 12 1 0 6 3 0 4 14 0
2021/202276 0 0 7 4 15 3 1 8 12 0 11 15
2022/2023140 17 21 10 15 16 11 2 17 15 5 4 7
2023/2024122 9 13 16 7 15 14 8 11 0 20 2 7
2024/202559 8 18 16 17 0 0 0 0 0 0 0 0
Totale 517