Catalogo dei prodotti della ricerca

UNOLT, MARTA
 Distribuzione geografica
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Continente #
NA - Nord America 1.127
EU - Europa 283
AS - Asia 226
SA - Sud America 10
AF - Africa 4
Totale 1.650
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Nazione #
US - Stati Uniti d'America 1.119
IT - Italia 123
SG - Singapore 96
CN - Cina 63
IN - India 55
SE - Svezia 50
FI - Finlandia 24
DE - Germania 19
AR - Argentina 10
BG - Bulgaria 10
FR - Francia 10
GB - Regno Unito 9
RO - Romania 7
CA - Canada 6
IE - Irlanda 6
ID - Indonesia 5
RU - Federazione Russa 5
CH - Svizzera 4
NL - Olanda 4
TG - Togo 4
UA - Ucraina 4
BE - Belgio 3
DK - Danimarca 2
IL - Israele 2
PH - Filippine 2
AE - Emirati Arabi Uniti 1
BS - Bahamas 1
ES - Italia 1
GL - Groenlandia 1
JP - Giappone 1
LT - Lituania 1
SI - Slovenia 1
TR - Turchia 1
Totale 1.650
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Città #
Fairfield 200
Ashburn 103
Woodbridge 82
Chandler 81
Houston 81
Seattle 81
Cambridge 80
Singapore 79
Wilmington 65
Rome 42
Beijing 38
Princeton 31
Ann Arbor 28
Santa Clara 22
San Paolo di Civitate 20
San Diego 17
Helsinki 16
Lawrence 13
Plano 12
New York 10
Sofia 10
Boston 9
Federal 9
Millbury 9
Andover 7
Pescara 7
Dearborn 6
Dublin 6
Campobasso 5
Hyderabad 5
Jakarta 5
Moscow 5
Lomé 4
Milan 4
Norwalk 4
Bern 3
Brussels 3
Changsha 3
Falkenstein 3
Falls Church 3
Lappeenranta 3
Nuremberg 3
Toronto 3
Boardman 2
Bühl 2
Forlì 2
Genoa 2
Gentofte Municipality 2
Hadera 2
Jinan 2
Kunming 2
Las Vegas 2
Los Angeles 2
Mannheim 2
Munich 2
Naples 2
Olongapo City 2
Ottawa 2
Parrano 2
Redwood City 2
Savona 2
Shenyang 2
Southend 2
Trumbull 2
Ardea 1
Bari 1
Bengaluru 1
Bucharest 1
Buenos Aires 1
Buffalo 1
Cassino 1
Catania 1
Chicago 1
Des Moines 1
Frankfurt am Main 1
Fremont 1
Gualtieri 1
Guangzhou 1
Harbin 1
Hebei 1
Hefei 1
Huzhou 1
Istanbul 1
Latina 1
Linyi 1
Little Rock 1
Ljubljana 1
Manchester 1
Marano di Napoli 1
Montréal 1
Nakano 1
Nanjing 1
Napoli 1
Nassau 1
Nieuwegein 1
Nuuk 1
Palma De Mallorca 1
Paris 1
Phoenix 1
Pisa 1
Totale 1.298
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Nome #
Factors that negatively affect the prognosis of pediatric community-acquired pneumonia in district hospital in Tanzania 89
Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo-Cardio-Facial) syndrome 79
Atypical cardiac defects in patients with RASopathies: updated data on CARNET study 79
Congenital heart disease and genetic syndromes: new insights into molecular mechanisms 78
Transposition of great arteries: new insights into the pathogenesis. 76
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers 76
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice. 69
Myoclonic epilepsy, parkinsonism, schizophrenia and left-handedness as common neuropsychiatric features in 22q11.2 deletion syndrome 69
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Double outlet right ventricle versus aortic dextroposition: morphologically distinct defects 64
Use of a pediatric syncope unit improves diagnosis and lowers costs: a hospital-based experience 56
Cardiac defects and genetic syndromes: old uncertainties and new insights 56
Congenital heart disease, genetic syndromes, and major noncardiac malformations 54
Congenital heart diseases in women 51
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Aortic arch interruption without ductus arteriosus and no ventricular septal defect 49
Left ventricular (LV) pacing in newborns and infants. Echo assessment of LV systolic function and synchrony at 5-year follow-up 47
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects 46
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion 46
Double-outlet left ventricle with l-malposition of the great arteries and subpulmonary ventricular septal defect 43
Smith-Lemli-Opitz syndrome, cardiac defects, and spleen anomalies 42
Atrioventricular septal defect prognosis for patients with down syndrome 42
Double-orifice left atrioventricular valve in patients with atrioventricular septal defect with and without down syndrome 41
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Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study 32
Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease 30
22q11.2 Deletion Syndrome. Impact of Genetics in the Treatment of Conotruncal Heart Defects 28
Coexisting genetic findings in a cohort of patients with laboratory confirmation of 22q11.2 deletion syndrome 26
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 24
Congenital heart defects in molecularly confirmed KBG syndrome patients 21
Some Isolated Cardiac Malformations Can Be Related to Laterality Defects 18
Impact of genetic studies on comprehension and treatment of congenital heart disease 18
22q and two: 22q11.2 deletion syndrome and coexisting conditions 16
Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome 12
What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia 10
Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome 7
Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age 6
Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition 6
Totale 1.776
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Categoria #
all - tutte 6.481
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 6.481
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020311 0 0 0 0 0 0 74 76 65 49 30 17
2020/2021174 13 22 8 34 4 22 11 14 20 6 12 8
2021/2022309 0 5 18 10 51 14 6 32 41 18 73 41
2022/2023293 53 48 19 10 43 27 6 18 40 8 12 9
2023/2024198 18 30 16 12 13 25 6 18 2 31 13 14
2024/2025173 9 30 29 20 42 40 3 0 0 0 0 0
Totale 1.776