IRIS
BONIOLI, EUGENIO
 Distribuzione geografica
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Continente #
EU - Europa 12.588
AS - Asia 1.443
NA - Nord America 1.360
SA - Sud America 118
AF - Africa 17
Continente sconosciuto - Info sul continente non disponibili 5
OC - Oceania 2
Totale 15.533
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Nazione #
IT - Italia 12.343
US - Stati Uniti d'America 1.283
SG - Singapore 611
CN - Cina 383
VN - Vietnam 200
FR - Francia 108
BD - Bangladesh 90
BR - Brasile 63
HK - Hong Kong 60
DE - Germania 45
JP - Giappone 28
CA - Canada 27
CH - Svizzera 24
FI - Finlandia 23
AR - Argentina 21
GB - Regno Unito 19
MX - Messico 18
CO - Colombia 14
IQ - Iraq 10
IN - India 8
CL - Cile 7
PK - Pakistan 7
HN - Honduras 6
JM - Giamaica 6
PH - Filippine 6
TH - Thailandia 6
ID - Indonesia 5
NL - Olanda 5
RU - Federazione Russa 5
VE - Venezuela 5
EC - Ecuador 4
GT - Guatemala 4
IE - Irlanda 4
TR - Turchia 4
TW - Taiwan 4
ZA - Sudafrica 4
CR - Costa Rica 3
ES - Italia 3
JO - Giordania 3
NI - Nicaragua 3
PY - Paraguay 3
SA - Arabia Saudita 3
TT - Trinidad e Tobago 3
AE - Emirati Arabi Uniti 2
AL - Albania 2
DZ - Algeria 2
EG - Egitto 2
GR - Grecia 2
KE - Kenya 2
KR - Corea 2
MA - Marocco 2
MY - Malesia 2
PA - Panama 2
SV - El Salvador 2
AM - Armenia 1
AU - Australia 1
BB - Barbados 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CG - Congo 1
CW - ???statistics.table.value.countryCode.CW??? 1
DO - Repubblica Dominicana 1
GH - Ghana 1
GP - Guadalupe 1
KG - Kirghizistan 1
KW - Kuwait 1
MD - Moldavia 1
MN - Mongolia 1
NG - Nigeria 1
NZ - Nuova Zelanda 1
OM - Oman 1
PL - Polonia 1
PT - Portogallo 1
QA - Qatar 1
SC - Seychelles 1
SE - Svezia 1
TG - Togo 1
UA - Ucraina 1
UZ - Uzbekistan 1
Totale 15.529
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Città #
Genova 7.193
Genoa 2.643
Rapallo 1.381
Vado Ligure 975
San Jose 444
Singapore 270
Lauterbourg 104
Ashburn 97
Hong Kong 59
Hanoi 58
Beijing 55
Ho Chi Minh City 55
Santa Clara 55
New York 49
Frankfurt am Main 41
Bordighera 37
Tokyo 25
Zurich 24
Chicago 23
Helsinki 23
Dallas 14
Los Angeles 14
Mexico City 13
Milan 13
Rome 13
Atlanta 9
City of London 9
Antioch 8
Tianjin 8
Buffalo 7
Charlotte 7
Da Nang 7
Miami 7
Naples 7
Brooklyn 6
Garland 6
Haiphong 6
São Paulo 6
Amsterdam 5
Baghdad 5
Cardiff 5
Figino 5
Greensboro 5
Guangzhou 5
Philadelphia 5
San Francisco 5
Santiago 5
Bologna 4
Collingswood 4
Columbus 4
Dhaka 4
Dublin 4
Federal Way 4
Florence 4
Fort Worth 4
Guatemala City 4
Montgomery 4
Porto Alegre 4
San Antonio 4
Turin 4
Alpharetta 3
Amman 3
Augusta 3
Austin 3
Bethlehem 3
Biên Hòa 3
Catania 3
Curitiba 3
Denver 3
Des Moines 3
Houston 3
Katy 3
Lahore 3
Las Vegas 3
Louisville 3
Milwaukee 3
Poplar 3
Princeton 3
Providence 3
Seattle 3
Shanghai 3
Toronto 3
Agawam 2
Ancona 2
Baltimore 2
Bangkok 2
Basra 2
Baton Rouge 2
Bogotá 2
Boston 2
Buenos Aires 2
Bắc Ninh 2
Cairo 2
Can Tho 2
Casablanca 2
Cleveland 2
Council Bluffs 2
Crofton 2
Davenport 2
Dearborn 2
Totale 13.970
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Nome #
Combined deficiency of xanthine oxidase and sulphite oxidase due to a deficiency of molybdenum cofactor. 208
Ten novel mutations in the human neurofibromatosis type 1 (NF1) gene in Italian patients 197
Asymptomatic intracranial hypertension associated with tetracycline use. 193
Altered response to stimuli of the AP-1/DNA binding activity in a syndrome of precocious ageing (Geroderma osteodysplastica hereditaria). 175
Therapy for hereditary nephrogenic diabetes insipidus. 172
Chyliferous vessel pathologies and associated syndromes: Primary chylous ascites 170
Heterozygous mutations of growth hormone receptor gene in children with idiopathic short stature. 169
The lymphatics in the pathophysiology of thoracic and abdominal surgical pathology: immunological consequences and the unexpected role of microsurgery 168
Congenital pulmonary lymphangiectasia. 167
Are there lymphatic vessels in the placenta? 164
Slipped capital femoral epiphysis associated with Rubinstein-Taybi syndrome. 163
Pseudolithiasis and intractable hiccups in a boy receiving ceftriaxone. 163
A diagnostic flow chart for non-immune hydrops fetalis. 160
Partial agenesis of corpus callosum in LEOPARD syndrome 160
Reliability assessment of glucose measurement by HemoCue analyser in a neonatal intensive care unit 160
Evaluation of tibial osteopathy occurrence in neurofibromatosis type 1 Italian patients. 160
Clinical picture of multiple anomalies in a 49,XXXXY patient 157
Immunohistochemistry in non-immune hydrops fetalis: a single center experience in 79 fetuses 155
Surgical vs. medical treatment of seizures in hemimegalencephaly. 154
X-linked creatine transporter deficiency: clinical description of a patient with a novel SLC6A8 gene mutation. 154
Microsurgery for treatment of peripheral lymphedema: long-term outcome and future perspectives 152
Microsurgery for lymphedema: clinical research and long-term results 151
Reliability assessment of glucose measurement by HemoCue analyzer in a neonatal intensive care unit: reply to Dr. Joakim Hagvik 149
Neurofibromatosis type 1 (NF1): Identification of eight unreported mutations in NF1 gene in Italian patients 148
Familial mediterranean fever 148
Aplasia cutis congenita, skull defect, brain heterotopia, and intestinal lymphangiectasia 148
Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome. 147
The role of lymphoscintigraphy in the diagnosis of lymphedema in Turner syndrome. 143
Clinical and cytogenetic study of a case of trisomy 1q with familial translocation t(1;5)(q42;p15.3) 143
Rubinstein-Taybi syndrome and pheochromocytoma 141
Unusual association: Dandy-Walker-like malformation in the Rubinstein-Taybi syndrome 140
Peroxisomal acyl-CoA-oxidase deficiency: two new cases 140
Paraproteinemia ina case of Hyper IgE syndrome in pediatric age. 140
Pulmonary lymphangiectasia. 139
Diagnosis and management of primary chylous ascites 139
Fumarate hydratase deficiency. 139
Inheritance of Rubinstein-Taybi syndrome. 138
Nuchal translucency and lymphatic system maldevelopment 138
Normal polymorphonuclear neutrophil function in a case of glycogen storage disease type Ib. 137
Sebaceous nevus syndrome: report of two cases 136
Lymphodysplasia and KRAS mutation: a case report and literature review 136
Congenital fetal and neonatal visceral chylous effusions: neonatal chylothorax and chylous ascites revisited. A multicenter retrospective study. 135
Follicular cysts of the mandible. The diagnostic problems 134
The Genoa experience of prenatal diagnosis in NF1 134
Pediatric lymphedema and correlated syndromes: role of microsurgery 133
Lymphoscintigraphy in paediatric patients. 133
Teacher and courses evaluation by attending students in Genoa (Italy) Medical School 132
Etiology of nonimmune hydrops fetalis: a systematic review 131
Dynamics of pleural fluid effusion and chylothorax in the fetus and newborn: role of the lymphatic system. 130
Association of NF1 and neuroblastoma in a pediatric case 127
Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 126
Lymphoscintigraphy patterns in newborns and children with congenital lymphatic dysplasia. 125
Imaging findings in pulmonary lymphangiectasia 124
A very rare cause of a deglutition disorder: achalasia of the cricopharyngeal muscle 123
A case of partial trisomy 4p 122
Phenobarbital enhances sister chromatid exchanges in vivo. 121
Immunohistochemical studies in a hydroptic fetus with pulmonary lymphangiectasia and trisomy 21. 119
Neurofibromatosis type 1 (NF1): Identification of eight unreported mutations in NF1 gene in Italian patients [corrected]. 117
Fibrodysplasia ossificans progressiva (myositis ossificans progressiva) 116
Clinical and radiological aspects of hypochondroplasia. Description of 6 cases 116
Lymphoscinitigraphy: its use for surgery decisions 113
Craniosinostosi 112
The role of lymphoscintigraphy in lymphatic dysplasias of the newborns and children 112
Lymphatic dysplasias of the newborn and children: the role of lymphoscintigraphy 112
Role of the early lymphatic microsurgery in the combined tratment of peripheral lymphedema 111
The heterogeneity of oral-facial-digital anomalies. Report of a case of Mohr syndrome 111
Mental retardation with a 46,XX, 9q12+ karyotype 110
Jarcho-Levin syndrome. Description of a familial case and review of the literature 110
Congentital lymphatic dysplasias in newborns 110
Prevention and treatment of injuries to the lymphatic system 110
A new case of partial trisomy 8p 110
Behaviour of cholesterol HDL in diabetes mellitus in childhood 108
Thoracic duct and Pecquet cyst dysplasias: clinical patterns, diagnostics, and therapeutical strategies 108
Behaviour of the renin-aldosterone system in a case of pheochromocytoma 108
Cheilognatho-urano-staphyloschisis associated with t(Y;13) 107
Trisomy 22 107
The Weaver Smith syndrome 107
Five case of cri du chat syndrome 107
Linee guida assistenziali nel bambino con patologia metabolica e malformativa - vol III 106
Immunohistochemical evaluation of fetal lymphatic malformation 106
La sclerosi tuberosa 104
Facio-Femoral syndrome. Description of a case with monolateral femoral hypoplasia 104
Partial trisomy of the long arm of chromosome 4: a new syndrome 103
Interpretation of chromosome Y variants 103
EEC syndrome:report of two cases in a familiy 103
Selective D2-40 lymphatic endothelium immunoreactivity in developing human fetal skin appendages 101
La genetica dell'obesita' 101
Lymphatic dysplasias in newborns and children: the role of lymphoscintigraphy 101
Brachmann-Cornelia de Lange syndrome 101
Activity of the brown adipose tissue in children with type 1 diabetes 101
Study of the beta cell function in type I diabetes by the determination of peptide C after glucagon challenge 101
Congenital lymphatic dysplasia in Kabuki syndrome: first report of an unusual association 100
Familial hypercjolesterolemia. Study of low density lipoprotein receptors. Treatment with plasmapheresis 100
Smith-Lemli-Opitz syndrome. Description of two cases and review of the literature 100
Freeman-Sheldon syndrome. Description of 2 cases of probable recessive autosomal inheritance. 100
Radiological case of the month. Sinus pericranii. 99
Unusual association of Bourneville's tuberous sclerosis and progressive external ophtalmoplegia 99
Picture of the month. Cushing's syndrome due to topical corticosteroids 98
Pituitary dwarfism "Goldnhar like" multiple deformities in a patient with 18p- 98
Karyotype-phenotype correlation in partial trisomy 13. Report of a case due to maternal translocation 97
Totale 12.958
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Categoria #
all - tutte 48.759
article - articoli 44.017
book - libri 314
conference - conferenze 3.055
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.373
Totale 97.518
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.298 0 0 115 152 102 64 84 406 31 129 41 174
2022/20231.633 158 112 16 154 237 338 0 125 312 16 131 34
2023/2024614 45 102 14 85 29 87 45 50 24 34 33 66
2024/20252.029 64 201 133 99 283 261 117 361 68 68 200 174
2025/20263.303 436 68 110 162 533 324 637 141 220 272 184 216
2026/2027756 397 74 285 0 0 0 0 0 0 0 0 0
Totale 15.533