IRIS
NOBILI, Bruno
 Distribuzione geografica
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Continente #
NA - Nord America 3.162
EU - Europa 2.594
AS - Asia 1.164
SA - Sud America 149
AF - Africa 9
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 1
Totale 7.085
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Nazione #
US - Stati Uniti d'America 3.146
IE - Irlanda 783
UA - Ucraina 461
SG - Singapore 403
GB - Regno Unito 357
HK - Hong Kong 311
CN - Cina 297
IT - Italia 290
DE - Germania 243
SE - Svezia 151
BR - Brasile 139
FI - Finlandia 121
TR - Turchia 96
FR - Francia 74
GR - Grecia 69
BE - Belgio 20
CA - Canada 12
CZ - Repubblica Ceca 8
KR - Corea 8
IN - India 6
IQ - Iraq 6
IR - Iran 6
EU - Europa 5
SA - Arabia Saudita 5
AR - Argentina 4
NL - Olanda 4
ZA - Sudafrica 4
BD - Bangladesh 3
GE - Georgia 3
JP - Giappone 3
MX - Messico 3
PK - Pakistan 3
RU - Federazione Russa 3
UZ - Uzbekistan 3
CO - Colombia 2
EC - Ecuador 2
EG - Egitto 2
IS - Islanda 2
KZ - Kazakistan 2
VN - Vietnam 2
AU - Australia 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
CH - Svizzera 1
DZ - Algeria 1
ES - Italia 1
ID - Indonesia 1
JM - Giamaica 1
JO - Giordania 1
MA - Marocco 1
MD - Moldavia 1
NO - Norvegia 1
NP - Nepal 1
PH - Filippine 1
PL - Polonia 1
PS - Palestinian Territory 1
PT - Portogallo 1
RO - Romania 1
TN - Tunisia 1
TW - Taiwan 1
UY - Uruguay 1
VE - Venezuela 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 7.085
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Città #
Dublin 782
Jacksonville 692
Chandler 596
Santa Clara 350
Hong Kong 307
Singapore 126
Ann Arbor 125
Princeton 120
Medford 111
Boardman 104
San Mateo 87
Wilmington 78
Beijing 69
Caserta 69
Woodbridge 69
Nanjing 62
Bremen 48
Ashburn 40
Cambridge 30
Roxbury 29
New York 23
Dearborn 21
Düsseldorf 21
Brussels 20
Kunming 20
Istanbul 18
Jinan 18
Mountain View 16
Napoli 15
Des Moines 14
Grumo Nevano 13
Hefei 13
Nanchang 13
Auburn Hills 12
Norwalk 11
São Paulo 11
Guangzhou 10
Elora 9
Naples 9
Hangzhou 8
Milan 8
Munich 8
Belo Horizonte 7
Brno 7
Hebei 7
Helsinki 7
Los Angeles 7
Seoul 7
Shenyang 7
Tianjin 7
Houston 6
Redwood City 6
Zhengzhou 6
Curitiba 5
Lanzhou 5
Ningbo 5
Nocera Inferiore 5
Riyadh 5
Centrale 4
Changchun 4
Cutrofiano 4
Falls Church 4
Rio de Janeiro 4
Seattle 4
Shanghai 4
Cava 3
Central 3
Changsha 3
Città Sant'Angelo 3
Dallas 3
Fortaleza 3
Giussano 3
Jiaxing 3
Portici 3
San Sebastiano al Vesuvio 3
Santa Luzia 3
Taiyuan 3
Tashkent 3
Tbilisi 3
Tehran 3
Verona 3
Alexandria 2
Altamura 2
Amsterdam 2
Baghdad 2
Bogotá 2
Bologna 2
Brasília 2
Brescia 2
Campinas 2
Cape Town 2
Contagem 2
Contrada di Sotto 2
Dhaka 2
Dong Ket 2
Fairfield 2
Goiânia 2
Haikou 2
Johannesburg 2
Jundiaí 2
Totale 4.418
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Nome #
Cannabinoid receptor 2 as anti-obesity target: inflammation, fat storage and browning modulation. 148
Cannabinoid receptor 2-63 QQ varianti s associated with severe necroinflammation in chronic epatiti C 123
Association between cannabinoid receptor type 2 Q63R variant and oligo/polyarticular juvenile idiopathic arthritis 119
Ematologia 113
Endocannabinoid Research Group (ERG), Italy. The endovanilloid/endocannabinoid system: a new potential target for osteoporosis therapy. 97
Cannabinoid receptor 2 Q63R variant could modulate the relationship between childhood obesity and age at menarche 94
Endocrine function and bone disease during long-term chelation therapy with deferasirox in patients with β-thalassemia major. 87
Iron overload enhances human mesenchymal stromal cell growth and hampers matrix calcification 87
A case of cutaneous mastocytosis associated with A-G dysgammaglobulinemia 86
Association Between a Polymorphism in Cannabinoid Receptor 2 and Severe Necroinflammation in Patients With Chronic Hepatitis C. 83
CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura. 83
The cannabinoid receptor type 2 as mediator of mesenchymal stromal cell immunosuppressive properties. 82
ERITROCITOSI CONGENITA CAUSATA DA ALTERAZIONI DEL SISTEMA SENSORE DELL’OSSIGENO 80
PKCβII-mediated cross-talk of TRPV1/CB2 modulates the glucocorticoid-induced osteoclast overactivity 79
The 17-β-oestradiol inhibits osteoclast activity by increasing the cannabinoid CB2 receptor expression. 78
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range. 78
Vitamin A and infancy. Biochemical, functional, and clinical aspects 76
Vitamin A and infancy. Biochemical, functional, and clinical aspects 75
The cannabinoid receptor type 2 Q63R variant increases the risk of celiac disease: implication for a novel molecular biomarker and future therapeutic intervention. 74
The genetic ablation or pharmacological inhibition of TRPV1 signalling is beneficial for the restoration of quiescent osteoclast activity in ovariectomized mice. 73
EPO receptor gain-of-function causes hereditary polycythemia, alters CD34 cell differentiation and increases circulating endothelial precursors. 73
The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 function 73
[Sanfilippo's disease of type B. Study of the enzymatic deficiency in a family] 73
The endovanilloid/endocannabinoid system: A new potential target for osteoporosis therapy 72
CB2 and TRPV1 receptors oppositely modulate in vitro human osteoblast activity 72
Von Hippel-Lindau-dependent polycythemia is endemic on the island of Ischia: identification of a novel cluster. 70
A modification of the 'pink test' may improve the diagnosis of hereditary spherocytosis 70
The 17-estradiol inhibits osteoclast activity by increasing the cannabinoid CB2 receptor expression 70
[Antibiotic therapy: cephalosporins] 70
Concordanza tra visita oculistica e RM encefalo nello screening del glioma delle vie ottiche nei pazienti pediatrici con neurofibromatosi tipo 1 70
Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency 69
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibition 69
Spectrum of FANCA mutations in Italian Fanconi anemia patients: identification of six novel alleles and phenotypic characterization of the S858R variant 68
[Alpha thalassemia in Campania: results of a survey of 319 newborn infants] 68
Iron overload causes osteoporosis in Thalassemia Major patients through interaction with TRPV1 channels. 67
Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele 67
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. 67
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis 66
Effects of nebivolol on human platelet aggregation 66
Studio retrospettivo sulle complicanze emato-oncologiche nella neurofibromatosi tipo 1 in età pediatrica 66
Interaction between metabotropic and NMDA glutamate receptors participate in the periaqueductal grey pain modulatory system 65
[Fluorimetric determination of erythrocytic free protoporphyrins in evaluation of iron deficiency states] 65
Amoxicillin-induced hemolytic anemia in a child with glucose 6-phosphate isomerase deficiency 65
[A case of progeria associated with Uhl's syndrome] 65
Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis 62
Treatment with short-term, high-dose cyclosporin A in children with refractory chronic idiopathic thrombocytopenic purpura 62
[Current possibilities of the use of ferritin in clinical diagnosis] 61
[Diagnostic methods in iron deficiency states. Comparative data on free protoporphyrins of erythrocytes in iron deficiency states and in thalassemia] 61
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 60
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 60
Rituximab (anti-CD20 monoclonal antibody) in children with chronic refractory symptomatic immune thrombocytopenic purpura: efficacy and safety of treatment 59
[Comparative evaluation of the activity "in vitro" of 4 aminoglycosides (gentamycin, sisomicin, tobramycin, amikacin)] 59
[An unusual salt-losing syndrome: pseudohypoaldosteronism. Description of a case] 59
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience 59
Factors influencing post-transfusional platelet increment in pediatric patients given hematopoietic stem cell transplantation 58
[Glycerol test in thalassemia diagnosis (author's transl)] 58
Bart's hemoglobin in newborn infants of Campania 58
Effect of eradication of Helicobacter pylori in children with chronic immune thrombocytopenia: a prospective, controlled, multicenter study. 57
COINHERITANCE OF GILBERT SYNDROME INCREASES THE RISK FOR DEVELOPING GALLSTONES IN PATIENTS WITH HEREDITARY SPHEROCYTOSIS 57
Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases 57
[Problems of antibiotic therapy in pediatrics] 57
Long-term efficacy of deferasirox for cardiac siderosis in thalassemia major 57
ROBO2 gene variants are associated with familial vesicoureteral reflux 56
Long-term follow-up analysis after rituximab therapy in children with refractory symptomatic ITP: identification of factors predictive of a sustained response 56
[Hematological screening of a group of children from a school population] 56
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 55
Reversible erythrocyte skeleton destabilization is modulated by beta-spectrin phosphorylation in childhood leukemia 55
Bilateral neuroretinitis in a 6-year-old boy with acquired toxoplasmosis 55
[Cartilage-hair hypoplasia: clinical and immunological study] 55
[Prevention therapy of infections in the course of granulocytopenia] 55
La prevenzione dell’anemia mediterranea in Campania: stato attuale e prospettive 55
Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis 54
Hereditary spherocytosis due to a novel frameshift mutation in AE1 cytoplasmic COOH terminal tail: band 3 Vesuvio 54
Serum Hepcidin and Iron Absorption in Pediatric Inflammatory Bowel Disease. 54
Long term efficacy of iron chelation therapy with deferasirox on endocrine function in thalassemia major 54
Flow-cytometric analysis of erythrocytes and reticulocytes in congenital dyserythropoietic anaemia type II (CDA II): value in differential diagnosis with hereditary spherocytosis 53
Anti-CD20 monoclonal antibody for the treatment of severe, immune-mediated, pure red cell aplasia and hemolytic anemia 53
Le anemie diseritropoietiche 53
[The L-dopa test in diagnosis of pituitary dwarfism] 53
[Fetal hemoglobin during the first year of life: evaluation of total erythrocytes, neocytes and gerocytes] 53
[Very unusual combination: congenital nephrosis and bilateral congenital glaucoma] 53
Terapia con rHu Epo in un caso di diabete mellito “early onset” ed anemia aplastica normocitica 53
Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II) 52
EVALUATION OF BODY IRON STATUS IN ITALIAN CARRIERS OF BETA-THALASSEMIA TRAIT 52
Diamond-Blackfan anaemia in the Italian population 52
Rituximab for the treatment of refractory autoimmune hemolytic anemia in children 52
Erythropoietin treatment can prevent blood transfusion in infantile pyknocytosis 51
ROBO2 gene variants are associated with familial vesicouretral reflux 51
Molecular heterogeneity of hereditary elliptocytosis in Italy 51
Anti-CD20 monoclonal antibody (Rituximab) for life-threatening autoimmune haemolytic anaemia in a patient with systemic lupus erythematosus 51
Management of acute childhood idiopathic thrombocytopenic purpura according to AIEOP consensus guidelines:assessment of Italian experience 50
Membranous glomerulopathy in children given allogeneic hematopoietic stem cell transplantation 50
Gender- and age-related distinctions for the in vivo prooxidant state in Fanconi anaemia patients 50
Clinical and molecular evaluation of non-dominant hereditary spherocytosis 50
The DMT1 IVS4+44C>A polymorphism and the risk of iron deficiency anemia in children with celiac disease 49
Splenectomy in children with chronic ITP: long-term efficacy and relation between its outcome and responses to previous treatments 48
Successful umbilical cord blood transplantation in a child with dyskeratosis congenita after a fludarabine-based reduced-intensity conditioning regimen 47
Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature 47
Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotype 47
[Prenatal diagnosis: current knowledge and future prospects] 47
Totale 6.504
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Categoria #
all - tutte 29.803
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 29.803
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202066 0 0 0 0 0 0 0 0 0 21 39 6
2020/20211.005 112 1 129 59 170 5 137 110 3 147 100 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
2024/20251.247 9 18 19 71 288 154 274 160 241 13 0 0
Totale 7.280