NOBILI, Bruno
 Distribuzione geografica
Continente #
EU - Europa 7.056
NA - Nord America 3.964
AS - Asia 2.901
SA - Sud America 414
AF - Africa 25
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 2
Totale 14.368
Nazione #
RU - Federazione Russa 4.316
US - Stati Uniti d'America 3.908
SG - Singapore 997
CN - Cina 793
IE - Irlanda 786
UA - Ucraina 465
HK - Hong Kong 410
GB - Regno Unito 375
BR - Brasile 358
IT - Italia 325
DE - Germania 281
VN - Vietnam 268
SE - Svezia 154
FI - Finlandia 124
IN - India 121
TR - Turchia 103
FR - Francia 84
GR - Grecia 69
KR - Corea 57
JP - Giappone 54
CA - Canada 28
AR - Argentina 23
BE - Belgio 20
BD - Bangladesh 17
PL - Polonia 16
MX - Messico 15
IQ - Iraq 10
CZ - Repubblica Ceca 9
SA - Arabia Saudita 9
EC - Ecuador 8
NL - Olanda 8
PH - Filippine 8
ZA - Sudafrica 8
IR - Iran 7
CO - Colombia 6
ES - Italia 6
PY - Paraguay 6
UZ - Uzbekistan 6
VE - Venezuela 6
AE - Emirati Arabi Uniti 5
EU - Europa 5
AT - Austria 4
CL - Cile 4
DO - Repubblica Dominicana 4
ID - Indonesia 4
KZ - Kazakistan 4
PK - Pakistan 4
TN - Tunisia 4
CR - Costa Rica 3
DZ - Algeria 3
GE - Georgia 3
MY - Malesia 3
PT - Portogallo 3
AU - Australia 2
AZ - Azerbaigian 2
EG - Egitto 2
IS - Islanda 2
JM - Giamaica 2
JO - Giordania 2
KE - Kenya 2
KW - Kuwait 2
MA - Marocco 2
MD - Moldavia 2
NP - Nepal 2
PS - Palestinian Territory 2
SN - Senegal 2
AF - Afghanistan, Repubblica islamica di 1
AO - Angola 1
BB - Barbados 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CH - Svizzera 1
EE - Estonia 1
ET - Etiopia 1
GT - Guatemala 1
HN - Honduras 1
IL - Israele 1
LT - Lituania 1
LV - Lettonia 1
NO - Norvegia 1
OM - Oman 1
PA - Panama 1
PE - Perù 1
QA - Qatar 1
RO - Romania 1
SY - Repubblica araba siriana 1
TW - Taiwan 1
UY - Uruguay 1
XK - ???statistics.table.value.countryCode.XK??? 1
YE - Yemen 1
Totale 14.368
Città #
Moscow 1.535
Dublin 785
Jacksonville 692
Chandler 596
Hong Kong 404
Singapore 399
Santa Clara 354
San Jose 285
Ashburn 157
Ann Arbor 125
Princeton 120
Medford 111
Boardman 104
Bengaluru 103
Hefei 98
Beijing 97
San Mateo 87
Ho Chi Minh City 79
Wilmington 78
Hanoi 71
Caserta 69
Woodbridge 69
Dallas 65
Nanjing 62
Seoul 56
Bremen 48
New York 35
Munich 31
Cambridge 30
Roxbury 29
São Paulo 27
The Dalles 27
Dearborn 21
Düsseldorf 21
Istanbul 21
Kunming 21
Brussels 20
Los Angeles 20
Jinan 19
Da Nang 16
Guangzhou 16
Mountain View 16
Naples 15
Napoli 15
Warsaw 15
Des Moines 14
Grumo Nevano 13
Haiphong 13
Nanchang 13
Auburn Hills 12
Belo Horizonte 12
Curitiba 12
Tianjin 12
Council Bluffs 11
Norwalk 11
Rio de Janeiro 11
Zhengzhou 11
Chicago 10
Frankfurt am Main 10
Elora 9
Hangzhou 9
Orem 9
Atlanta 8
Milan 8
Shenyang 8
Boston 7
Brno 7
Hebei 7
Helsinki 7
Hillsboro 7
Houston 7
Nha Trang 7
London 6
Montreal 6
Ningbo 6
Redwood City 6
Riyadh 6
Shanghai 6
Tashkent 6
Bắc Ninh 5
Johannesburg 5
Lanzhou 5
Nocera Inferiore 5
Porto Alegre 5
Amsterdam 4
Baghdad 4
Brasília 4
Brooklyn 4
Campinas 4
Caracas 4
Centrale 4
Changchun 4
Changsha 4
Cutrofiano 4
Dhaka 4
Falls Church 4
Goiânia 4
Jiaxing 4
Recife 4
Ribeirão Preto 4
Totale 7.460
Nome #
Association between cannabinoid receptor type 2 Q63R variant and oligo/polyarticular juvenile idiopathic arthritis 246
Cannabinoid receptor 2 as anti-obesity target: inflammation, fat storage and browning modulation. 205
Cannabinoid receptor 2-63 QQ varianti s associated with severe necroinflammation in chronic epatiti C 203
Cannabinoid receptor 2 Q63R variant could modulate the relationship between childhood obesity and age at menarche 196
Association Between a Polymorphism in Cannabinoid Receptor 2 and Severe Necroinflammation in Patients With Chronic Hepatitis C. 189
Endocannabinoid Research Group (ERG), Italy. The endovanilloid/endocannabinoid system: a new potential target for osteoporosis therapy. 185
Iron overload enhances human mesenchymal stromal cell growth and hampers matrix calcification 184
CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura. 181
A case of cutaneous mastocytosis associated with A-G dysgammaglobulinemia 177
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range. 177
Endocrine function and bone disease during long-term chelation therapy with deferasirox in patients with β-thalassemia major. 168
[Sanfilippo's disease of type B. Study of the enzymatic deficiency in a family] 163
Ematologia 157
EPO receptor gain-of-function causes hereditary polycythemia, alters CD34 cell differentiation and increases circulating endothelial precursors. 156
PKCβII-mediated cross-talk of TRPV1/CB2 modulates the glucocorticoid-induced osteoclast overactivity 156
Vitamin A and infancy. Biochemical, functional, and clinical aspects 155
The cannabinoid receptor type 2 Q63R variant increases the risk of celiac disease: implication for a novel molecular biomarker and future therapeutic intervention. 155
The 17-β-oestradiol inhibits osteoclast activity by increasing the cannabinoid CB2 receptor expression. 152
A modification of the 'pink test' may improve the diagnosis of hereditary spherocytosis 152
The cannabinoid receptor type 2 as mediator of mesenchymal stromal cell immunosuppressive properties. 151
Association of the cannabinoid receptor 2 (CB2) Gln63Arg polymorphism with indices of liver damage in obese children: An alternative way to highlight the CB2 hepatoprotective properties. 151
[Fluorimetric determination of erythrocytic free protoporphyrins in evaluation of iron deficiency states] 150
Vitamin A and infancy. Biochemical, functional, and clinical aspects 147
ERITROCITOSI CONGENITA CAUSATA DA ALTERAZIONI DEL SISTEMA SENSORE DELL’OSSIGENO 147
The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 function 146
[Hematological screening of a group of children from a school population] 143
CB2 and TRPV1 receptors oppositely modulate in vitro human osteoblast activity 142
[Antibiotic therapy: cephalosporins] 142
Concordanza tra visita oculistica e RM encefalo nello screening del glioma delle vie ottiche nei pazienti pediatrici con neurofibromatosi tipo 1 142
The genetic ablation or pharmacological inhibition of TRPV1 signalling is beneficial for the restoration of quiescent osteoclast activity in ovariectomized mice. 141
Spectrum of FANCA mutations in Italian Fanconi anemia patients: identification of six novel alleles and phenotypic characterization of the S858R variant 139
[Current possibilities of the use of ferritin in clinical diagnosis] 137
Iron overload causes osteoporosis in Thalassemia Major patients through interaction with TRPV1 channels. 137
The 17-estradiol inhibits osteoclast activity by increasing the cannabinoid CB2 receptor expression 137
[Alpha thalassemia in Campania: results of a survey of 319 newborn infants] 137
[Glycerol test in thalassemia diagnosis (author's transl)] 136
[Prevention therapy of infections in the course of granulocytopenia] 136
[Comparative evaluation of the activity "in vitro" of 4 aminoglycosides (gentamycin, sisomicin, tobramycin, amikacin)] 135
[Diagnostic methods in iron deficiency states. Comparative data on free protoporphyrins of erythrocytes in iron deficiency states and in thalassemia] 135
[A case of progeria associated with Uhl's syndrome] 135
The endovanilloid/endocannabinoid system: A new potential target for osteoporosis therapy 133
[The L-dopa test in diagnosis of pituitary dwarfism] 133
Von Hippel-Lindau-dependent polycythemia is endemic on the island of Ischia: identification of a novel cluster. 132
[An unusual salt-losing syndrome: pseudohypoaldosteronism. Description of a case] 131
Amoxicillin-induced hemolytic anemia in a child with glucose 6-phosphate isomerase deficiency 131
Effects of nebivolol on human platelet aggregation 130
Interaction between metabotropic and NMDA glutamate receptors participate in the periaqueductal grey pain modulatory system 128
[Problems of antibiotic therapy in pediatrics] 128
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibition 125
Studio retrospettivo sulle complicanze emato-oncologiche nella neurofibromatosi tipo 1 in età pediatrica 125
[Very unusual combination: congenital nephrosis and bilateral congenital glaucoma] 124
Diamond-Blackfan anemia: expansion of erythroid progenitors in vitro by IL-9, but exclusion of a significant pathogenetic role for the IL-9 gene and the hematopoietic gene cluster on chromosome 5q 123
Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency 123
The endovanilloid/endocannabinoid system in human osteoclasts: Possible involvement in bone formation and resorption 123
Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele 122
[Fetal hemoglobin during the first year of life: evaluation of total erythrocytes, neocytes and gerocytes] 121
[Prenatal diagnosis: current knowledge and future prospects] 120
Neridronate improves bone mineral density and reduces back pain in β-thalassaemia patients with osteoporosis: results from a phase 2, randomized, parallel-arm, open-label study 119
[Cartilage-hair hypoplasia: clinical and immunological study] 119
The DMT1 IVS4+44C>A polymorphism and the risk of iron deficiency anemia in children with celiac disease 119
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis 117
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience 115
Treatment with short-term, high-dose cyclosporin A in children with refractory chronic idiopathic thrombocytopenic purpura 112
Long-term efficacy of deferasirox for cardiac siderosis in thalassemia major 111
Rituximab (anti-CD20 monoclonal antibody) in children with chronic refractory symptomatic immune thrombocytopenic purpura: efficacy and safety of treatment 109
La prevenzione dell’anemia mediterranea in Campania: stato attuale e prospettive 108
Reversible erythrocyte skeleton destabilization is modulated by beta-spectrin phosphorylation in childhood leukemia 107
L1 effects on reactive oxygen (ROS) and nitrogen species (RNS) release, hemoglobin oxidation, low molecular weight antioxidants, and antioxidant enzyme activities in red and white blood cells of thalassemic patients 107
Hereditary spherocytosis due to a novel frameshift mutation in AE1 cytoplasmic COOH terminal tail: band 3 Vesuvio 106
Esame emocromocitometrico 106
Bilateral neuroretinitis in a 6-year-old boy with acquired toxoplasmosis 104
Effect of eradication of Helicobacter pylori in children with chronic immune thrombocytopenia: a prospective, controlled, multicenter study. 103
ROBO2 gene variants are associated with familial vesicoureteral reflux 103
Diamond-Blackfan anaemia in the Italian population 103
Rituximab for the treatment of refractory autoimmune hemolytic anemia in children 103
Long-term follow-up analysis after rituximab therapy in children with refractory symptomatic ITP: identification of factors predictive of a sustained response 102
Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis 102
COINHERITANCE OF GILBERT SYNDROME INCREASES THE RISK FOR DEVELOPING GALLSTONES IN PATIENTS WITH HEREDITARY SPHEROCYTOSIS 102
Factors influencing post-transfusional platelet increment in pediatric patients given hematopoietic stem cell transplantation 102
Le anemie diseritropoietiche 102
REPORT OF ADVERSE TRANSFUSION REACTIONS: EMOCOMPONENTS VIA APHERESIS VS WHOLE BLOOD INPEDIATRIC PATIENTS 102
Clinical and biochemical study of thalassemia intermedia in Campania (southern Italy) 101
Management of acute childhood idiopathic thrombocytopenic purpura according to AIEOP consensus guidelines:assessment of Italian experience 100
Membranous glomerulopathy in children given allogeneic hematopoietic stem cell transplantation 100
Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis 100
Clinical and molecular evaluation of non-dominant hereditary spherocytosis 100
Serum Hepcidin and Iron Absorption in Pediatric Inflammatory Bowel Disease. 100
The outcome of children with Fanconi anemia given hematopoietic stem cell transplantation and the influence of fludarabine in the conditioning regimen: a report from the Italian pediatric group 99
Anti-CD20 monoclonal antibody (Rituximab) for life-threatening autoimmune haemolytic anaemia in a patient with systemic lupus erythematosus 99
Long term efficacy of iron chelation therapy with deferasirox on endocrine function in thalassemia major 99
Flow-cytometric analysis of erythrocytes and reticulocytes in congenital dyserythropoietic anaemia type II (CDA II): value in differential diagnosis with hereditary spherocytosis 98
Gender- and age-related distinctions for the in vivo prooxidant state in Fanconi anaemia patients 97
ROBO2 gene variants are associated with familial vesicouretral reflux 97
Molecular heterogeneity of hereditary elliptocytosis in Italy 97
EVALUATION OF BODY IRON STATUS IN ITALIAN CARRIERS OF BETA-THALASSEMIA TRAIT 96
Bart's hemoglobin in newborn infants of Campania 96
Terapia con rHu Epo in un caso di diabete mellito “early onset” ed anemia aplastica normocitica 96
Erythropoietin treatment can prevent blood transfusion in infantile pyknocytosis 95
Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II) 95
Anti-CD20 monoclonal antibody for the treatment of severe, immune-mediated, pure red cell aplasia and hemolytic anemia 95
Totale 12.918
Categoria #
all - tutte 45.641
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 45.641


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021279 0 0 0 0 0 0 0 0 0 147 100 32
2021/2022763 96 8 7 18 257 7 13 19 27 72 66 173
2022/20231.814 144 40 27 205 206 176 3 134 804 13 33 29
2023/2024537 69 14 22 65 196 29 15 25 4 0 29 69
2024/20251.649 9 18 19 71 288 154 274 160 241 224 108 83
2025/20266.881 256 322 340 300 587 4.075 405 244 234 118 0 0
Totale 14.563