Catalogo dei prodotti della ricerca

MARINO TAUSSIG DE BODONIA, Bruno
 Distribuzione geografica
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Continente #
NA - Nord America 8.956
EU - Europa 1.964
AS - Asia 1.322
AF - Africa 39
SA - Sud America 37
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 12.323
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Nazione #
US - Stati Uniti d'America 8.908
UA - Ucraina 574
IT - Italia 549
SG - Singapore 442
IN - India 422
CN - Cina 394
SE - Svezia 247
FI - Finlandia 217
DE - Germania 85
GB - Regno Unito 54
IE - Irlanda 48
CA - Canada 41
NL - Olanda 39
RU - Federazione Russa 38
AR - Argentina 34
BE - Belgio 33
TG - Togo 24
BG - Bulgaria 23
ID - Indonesia 18
FR - Francia 16
RO - Romania 13
CH - Svizzera 12
IR - Iran 7
HK - Hong Kong 6
ZA - Sudafrica 6
MX - Messico 5
NG - Nigeria 5
PT - Portogallo 5
SA - Arabia Saudita 5
IL - Israele 4
JP - Giappone 4
KR - Corea 4
TR - Turchia 4
BR - Brasile 3
ES - Italia 3
PH - Filippine 3
AE - Emirati Arabi Uniti 2
AU - Australia 2
CZ - Repubblica Ceca 2
DK - Danimarca 2
EU - Europa 2
SC - Seychelles 2
TW - Taiwan 2
AZ - Azerbaigian 1
BN - Brunei Darussalam 1
BS - Bahamas 1
BY - Bielorussia 1
EG - Egitto 1
GL - Groenlandia 1
LT - Lituania 1
MU - Mauritius 1
NZ - Nuova Zelanda 1
PK - Pakistan 1
PL - Polonia 1
SI - Slovenia 1
TH - Thailandia 1
VN - Vietnam 1
Totale 12.323
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Città #
Fairfield 1.642
Woodbridge 897
Houston 744
Seattle 618
Ashburn 613
Cambridge 566
Wilmington 488
Chandler 476
Ann Arbor 376
Singapore 311
Beijing 293
Princeton 282
Rome 262
Jacksonville 240
Plano 190
Boston 156
Lawrence 154
Santa Clara 120
San Diego 117
San Paolo di Civitate 96
Millbury 71
Dearborn 59
Andover 52
Dublin 48
New York 47
Boardman 46
Falls Church 43
Helsinki 41
Norwalk 36
Federal 32
Toronto 29
Pune 25
Lomé 24
Sofia 23
Los Angeles 22
Moscow 22
Falkenstein 19
Waanrode 19
Jakarta 18
Des Moines 16
Milan 16
San Mateo 14
Brussels 13
Hyderabad 12
Bühl 11
Bern 9
London 9
Mannheim 9
Guangzhou 8
Nanjing 8
Redmond 8
Changsha 7
Hefei 7
Lappeenranta 7
Ottawa 7
Pescara 7
Bari 6
Hong Kong 6
Campobasso 5
Kunming 5
Port Harcourt 5
Ancona 4
Bremen 4
Buffalo 4
Cordova 4
Grafing 4
Indiana 4
Jinan 4
Kilburn 4
Phoenix 4
Prineville 4
Redwood City 4
Trumbull 4
Acqui Terme 3
Bologna 3
Bolzano 3
Dallas 3
Hebei 3
Macomer 3
Merano 3
Mexico City 3
Nanchang 3
Shenyang 3
Zhengzhou 3
Acton 2
Auburn Hills 2
Buenos Aires 2
Campofelice Di Roccella 2
Chicago 2
Craigavon 2
Cumming 2
Feira de Santana 2
Fiumicino 2
Forlì 2
Frankfurt am Main 2
Fremont 2
Genoa 2
Gentofte Municipality 2
Groningen 2
Harbin 2
Totale 9.625
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Nome #
A genetic assessment of trisomy 21 in a patient with persistent truncus arteriosus who died 38 years ago 112
Shells and heart: Are human laterality and chirality of snails controlled by the same maternal genes? 102
Cardiopulmonary response to exercise and cardiac assessment in patients with turner syndrome. 99
The heart and shell. Anatomical and genetic similarities 98
Absent pulmonary valve with intact ventricular septum and patent ductus arteriosus: a specific cardiac phenotype associated with deletion 18q syndrome 95
Surgical Outcomes for Patients with Turner Syndrome. 91
Atrioventricular canal defect and genetic syndromes: the unifying role of sonic hedgehog 89
Influence of heart rate on left ventricular isovolumic relaxation time: a Doppler study in healthy newborns 89
Association of deletion 22 and trisomy 21: A likely random association in patients with conotruncal heart defects 87
Familial recurrence of discrete membranous subaortic stenosis 86
Truncus Arteriosus with Unilateral Absence of the Left Proximal Pulmonary Artery and DiGeorge Syndrome 86
DiGeorge subtypes of nonsyndromic conotruncal defects: evidence against a major role of TBX1 Gene 82
Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome 82
Persistent left superior vena cava into unroofed coronary sinus 81
Specific congenital heart defects in RSH/Smith-Lemli-Opitz syndrome: Postulated involvement of the sonic hedgehog pathway in syndromes with postaxial polydactyly or heterotaxia 81
Prevalence, type, and molecular spectrum of NF1 mutations in patients with neurofibromatosis type 1 and congenital heart disease 81
Additional evidence that PTPN11 mutations play only a minor role in the pathogenesis of non-syndromic atrioventricular canal defect 81
Comparison of left ventricular ejection fraction by magnetic resonance imaging and radionuclide ventriculography in idiopathic dilated cardiomyopathy 80
Association of Di George anomaly and caudal dysplasia sequence in neonate born to a diabetic mother. 80
Outcome in Down syndrome fetuses with cardiac anomalies 80
Genetic syndromes and congenital heart defects: how is surgical management affected? 80
Three patients with oculo-auriculo-vertebral spectrum and microdeletion 22q11.2 79
Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo-Cardio-Facial) syndrome 79
Common atrium/atrioventricular canal defect and postaxial polydactyly: a mild clinical subtype of Ellis-van Creveld syndrome caused by hypomorphic mutations in the EVC gene 79
Genetic syndromes and outcome after surgical correction of tetralogy of Fallot 78
Congenital heart disease and genetic syndromes: new insights into molecular mechanisms 78
Atypical cardiac defects in patients with RASopathies: updated data on CARNET study 78
Autosomal dominant inheritance of aplasia cutis congenita and congenital heart defect: A possible link to the Adams-Oliver syndrome 78
No proof that Santa Rosa heart thrombus was antemortem – Authors' reply 77
Age at operation for children with atrioventricular canal. 77
Clinical and molecular analysis of 30 patients with multiple lentigines LEOPARD syndrome 77
Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors 77
Impact of DEL22q11, trisomy 21, and other genetic syndromes on surgical outcome of conotruncal heart defects 77
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
Cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results 76
Profilo anatomo-clinico dell'atresia aortica con difetto interventricolare 75
GATA4 as Candidate Gene for Pericardial Defects 75
Atrioventricular canal defect in patients with RASopathies 75
Congenital heart defect in sibs with discordant karyotypes 74
Cardiac outflow tract: A review of some embryogenetic aspects of the conotruncal region of the heart 74
Familial recurrence of transposition of the great arteries. 74
Better surgical prognosis for patients with Down Syndrome 73
Health supervision for children with down syndrome. 73
Blocked atrial bi/trigeminy in utero evolving in supraventricular tachycardia after birth. 73
Correlation between PTPN11 gene mutations and congenital heart defects in Noonan and LEOPARD syndromes 72
Atrioventricular canal defect and associated genetic disorders: new insights into polydactyly syndromes 72
Challenges of classifying double outlet right ventricle: Importance for genotype-phenotype analyses. 72
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries in mice 72
Re: Atrioventricular septal defect with common atrioventricular junction, common arterial trunk and severe coartation of the aorta in a patient with Down's syndrome. 71
Familial aggregation of genetically heterogeneous hypertrophic cardiomyopathy: a boy with LEOPARD syndrome due to PTPN11 mutation and his nonsyndromic father lacking PTPN11 mutations 71
Congenital diaphragmatic hernia after exposure to a triple retinoic acid antagonist during pregnancy 71
New mutations in ZFPM2/FOG2 gene in tetralogy of fallot and double outlet right ventricle 71
Atrioventricular canal defect as a sign of laterality defect in Ellis-van Creveld and polydactyly syndromes with ciliary and hedgehog signaling dysfunction 71
Congenital heart defects in Noonan syndrome and RIT1 mutation 70
Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect 70
Tetralogy of Fallot with aortic valvular stenosis and deletion 22q11 69
New Findings concerning Cardiovascular Manifestations emerging from Long-term Follow-up of 150 patients with the Williams-Beuren-Beuren syndrome 69
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice. 69
Complete transposition of the great arteries: patterns of congenital heart disease in familial precurrence 69
Deletion 22q11 in patients with interrupted aortic arch. 68
Ductal origin of the distal pulmonary artery in truncus arteriosus. 68
NF1 gene mutations represent the major molecular event underlying neurofibromatosis-Noonan syndrome 68
Congenital heart defects in patients with oculo-auriculo-vertebral spectrum (Goldenhar syndrome) 68
Cardiac defects in Mexican children with down syndrome 67
PTPN11 gene mutations: linking the Gln510Glu mutation to the "LEOPARD syndrome phenotype" 67
22q11 Deletion syndrome: a review of some developmental biology aspects of the cardiovascular system 67
Severe, obstructive biventricular hypertrophy in a patient with Costello syndrome: Clinical impact and management 66
Genetic predisposition to ventricular septal defect in Down syndrome 66
T cell receptor repertoire and function in patients with DiGeroge syndrome and velocardiofacial syndrome 65
Familial transposition of the great arteries caused by multiple mutations in laterality genes 65
Screening for 22q11.2 microdeletion in adults with tetralogy of Fallot 65
Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: rare association with pulmonary valve stenosis 65
JAG1 Mutation in a patient with deletion 22q11.2 syndrome and tetralogy of Fallot 65
null 65
Cardiovascular disease in Down syndrome 65
A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot 65
Atrioventricular canal defect is the classic congenital heart disease in Bardet-Biedl syndrome 65
Better surgical prognosis for patients with complete atrioventricular septal defect and Down’s syndrome. 65
Hypoplastic Left Heart Syndrome in Patients With Kabuki Syndrome 65
LEOPARD syndrome: clinical diagnosis in the first year of life. 64
CRELD1 and GATA4 gene analysis in patients with nonsyndromic atrioventricular canal defects. 64
Types of cardiac defects in children with Down's syndrome. 64
Ebstein Anomaly: Genetic Heterogeneity and Association With Microdeletions 1p36 and 8p23.1 64
Spiral shapes in heart and shells: when form and function do matter 64
Surgery for Complex forms of Atrioventricular Septal Defect: Early Survival and Probability of Cure 64
Double outlet right ventricle versus aortic dextroposition: morphologically distinct defects 64
Spiral pattern: universe, normal heart and complex congenital defects. 63
Exclusion of Cx43 gene mutation as a major cause of criss-cross heart anomaly in man 63
Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome 63
Deletion 22q11 and isolated congenital heart disease 63
Transposition of the great arteries in asplenia and polysplenia phenotypes 63
Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects 63
Pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: the multifaceted consequences of PTPN11 mutations 63
FOLIC ACID AND METHIONINE IN THE PREVENTION OF TERATOGEN -INDUCED CONGENITAL DEFECTS IN MICE 63
Obituary of Dr. Angelo Di George 63
Genotype-phenotype analysis and natural history of left ventricular hypertrophy in LEOPARD syndrome. 63
Clinical, pathological, and molecular analyses of cardiovascular abnormalities in Costello syndrome: a Ras/MAPK pathway syndrome. 63
Atrioventricular canal defect in Bardet-Biedl syndrome: clinical evidence supporting the link between atrioventricular canal defect and polydactyly syndromes with ciliary dysfunction536. 62
Genetics of congenital heart diseases in syndromic and non-syndromic patients: new advances and clinical implications 62
Totale 7.314
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Categoria #
all - tutte 39.809
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 39.809
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.259 0 0 0 0 0 386 424 427 374 395 186 67
2020/20211.119 162 146 51 141 16 89 24 107 100 136 114 33
2021/20222.244 11 133 269 69 294 40 44 249 165 168 355 447
2022/20231.781 465 392 64 175 174 147 20 127 130 17 41 29
2023/2024884 68 133 41 67 53 99 19 57 16 148 64 119
2024/2025653 82 63 144 71 181 112 0 0 0 0 0 0
Totale 12.737