IRIS
NOBILI, Bruno
 Distribuzione geografica
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Continente #
NA - Nord America 2.917
EU - Europa 2.581
AS - Asia 607
Continente sconosciuto - Info sul continente non disponibili 5
SA - Sud America 5
AF - Africa 2
OC - Oceania 1
Totale 6.118
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Nazione #
US - Stati Uniti d'America 2.902
IE - Irlanda 783
UA - Ucraina 460
GB - Regno Unito 357
IT - Italia 289
CN - Cina 279
DE - Germania 240
SG - Singapore 195
SE - Svezia 151
FI - Finlandia 121
TR - Turchia 92
FR - Francia 74
GR - Grecia 68
BE - Belgio 18
CA - Canada 12
CZ - Repubblica Ceca 8
KR - Corea 8
IN - India 6
IR - Iran 6
EU - Europa 5
SA - Arabia Saudita 5
BR - Brasile 4
HK - Hong Kong 4
NL - Olanda 4
JP - Giappone 3
MX - Messico 3
EG - Egitto 2
GE - Georgia 2
IS - Islanda 2
VN - Vietnam 2
AR - Argentina 1
AU - Australia 1
BD - Bangladesh 1
CH - Svizzera 1
ES - Italia 1
IQ - Iraq 1
MD - Moldavia 1
PH - Filippine 1
PK - Pakistan 1
PL - Polonia 1
PT - Portogallo 1
RO - Romania 1
TW - Taiwan 1
Totale 6.118
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Città #
Dublin 782
Jacksonville 692
Chandler 596
Ann Arbor 125
Santa Clara 121
Singapore 121
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
Kunming 20
Brussels 18
Jinan 18
Mountain View 16
Napoli 15
Des Moines 14
Istanbul 14
Grumo Nevano 13
Hefei 13
Nanchang 13
Auburn Hills 12
Norwalk 11
Elora 9
Naples 9
Milan 8
Munich 8
Brno 7
Guangzhou 7
Hangzhou 7
Hebei 7
Helsinki 7
Seoul 7
Shenyang 7
Tianjin 7
Houston 6
Redwood City 6
Zhengzhou 6
Lanzhou 5
Los Angeles 5
Ningbo 5
Nocera Inferiore 5
Riyadh 5
Centrale 4
Changchun 4
Cutrofiano 4
Falls Church 4
Seattle 4
Cava 3
Central 3
Changsha 3
Città Sant'Angelo 3
Dallas 3
Giussano 3
Portici 3
San Sebastiano al Vesuvio 3
Taiyuan 3
Tehran 3
Verona 3
Alexandria 2
Altamura 2
Amsterdam 2
Bologna 2
Brescia 2
Contrada di Sotto 2
Dong Ket 2
Fairfield 2
Haikou 2
Jiaxing 2
Marano Di Napoli 2
Rome 2
Sarno 2
Selvazzano Dentro 2
Taizhou 2
Tbilisi 2
Tlalnepantla 2
Venice 2
Voghera 2
Ōbu 2
Bangalore 1
Barcelona 1
Bengaluru 1
Budenheim 1
Buffalo 1
Calvizzano 1
Candiolo 1
Castellammare Di Stabia 1
Catanzaro 1
Cercola 1
Totale 3.831
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Nome #
Cannabinoid receptor 2 as anti-obesity target: inflammation, fat storage and browning modulation. 126
Cannabinoid receptor 2-63 QQ varianti s associated with severe necroinflammation in chronic epatiti C 113
Ematologia 107
Association between cannabinoid receptor type 2 Q63R variant and oligo/polyarticular juvenile idiopathic arthritis 103
Cannabinoid receptor 2 Q63R variant could modulate the relationship between childhood obesity and age at menarche 88
Endocannabinoid Research Group (ERG), Italy. The endovanilloid/endocannabinoid system: a new potential target for osteoporosis therapy. 88
Iron overload enhances human mesenchymal stromal cell growth and hampers matrix calcification 81
Association Between a Polymorphism in Cannabinoid Receptor 2 and Severe Necroinflammation in Patients With Chronic Hepatitis C. 80
The cannabinoid receptor type 2 as mediator of mesenchymal stromal cell immunosuppressive properties. 75
A case of cutaneous mastocytosis associated with A-G dysgammaglobulinemia 74
Endocrine function and bone disease during long-term chelation therapy with deferasirox in patients with β-thalassemia major. 74
The 17-β-oestradiol inhibits osteoclast activity by increasing the cannabinoid CB2 receptor expression. 72
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range. 72
CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura. 70
ERITROCITOSI CONGENITA CAUSATA DA ALTERAZIONI DEL SISTEMA SENSORE DELL’OSSIGENO 69
PKCβII-mediated cross-talk of TRPV1/CB2 modulates the glucocorticoid-induced osteoclast overactivity 69
The genetic ablation or pharmacological inhibition of TRPV1 signalling is beneficial for the restoration of quiescent osteoclast activity in ovariectomized mice. 67
The cannabinoid receptor type 2 Q63R variant increases the risk of celiac disease: implication for a novel molecular biomarker and future therapeutic intervention. 66
The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 function 65
The endovanilloid/endocannabinoid system: A new potential target for osteoporosis therapy 64
Von Hippel-Lindau-dependent polycythemia is endemic on the island of Ischia: identification of a novel cluster. 64
The 17-estradiol inhibits osteoclast activity by increasing the cannabinoid CB2 receptor expression 64
Vitamin A and infancy. Biochemical, functional, and clinical aspects 64
Vitamin A and infancy. Biochemical, functional, and clinical aspects 63
[Sanfilippo's disease of type B. Study of the enzymatic deficiency in a family] 63
Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele 63
CB2 and TRPV1 receptors oppositely modulate in vitro human osteoblast activity 63
EPO receptor gain-of-function causes hereditary polycythemia, alters CD34 cell differentiation and increases circulating endothelial precursors. 62
Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency 62
Iron overload causes osteoporosis in Thalassemia Major patients through interaction with TRPV1 channels. 62
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibition 61
Concordanza tra visita oculistica e RM encefalo nello screening del glioma delle vie ottiche nei pazienti pediatrici con neurofibromatosi tipo 1 61
Studio retrospettivo sulle complicanze emato-oncologiche nella neurofibromatosi tipo 1 in età pediatrica 61
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis 60
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. 60
[Antibiotic therapy: cephalosporins] 59
Interaction between metabotropic and NMDA glutamate receptors participate in the periaqueductal grey pain modulatory system 58
Spectrum of FANCA mutations in Italian Fanconi anemia patients: identification of six novel alleles and phenotypic characterization of the S858R variant 57
Effects of nebivolol on human platelet aggregation 57
[Fluorimetric determination of erythrocytic free protoporphyrins in evaluation of iron deficiency states] 57
Amoxicillin-induced hemolytic anemia in a child with glucose 6-phosphate isomerase deficiency 57
A modification of the 'pink test' may improve the diagnosis of hereditary spherocytosis 55
Rituximab (anti-CD20 monoclonal antibody) in children with chronic refractory symptomatic immune thrombocytopenic purpura: efficacy and safety of treatment 54
[Alpha thalassemia in Campania: results of a survey of 319 newborn infants] 54
[A case of progeria associated with Uhl's syndrome] 54
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience 54
Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis 53
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 53
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 53
Effect of eradication of Helicobacter pylori in children with chronic immune thrombocytopenia: a prospective, controlled, multicenter study. 52
COINHERITANCE OF GILBERT SYNDROME INCREASES THE RISK FOR DEVELOPING GALLSTONES IN PATIENTS WITH HEREDITARY SPHEROCYTOSIS 52
Bart's hemoglobin in newborn infants of Campania 52
Long-term efficacy of deferasirox for cardiac siderosis in thalassemia major 52
ROBO2 gene variants are associated with familial vesicoureteral reflux 51
Factors influencing post-transfusional platelet increment in pediatric patients given hematopoietic stem cell transplantation 50
[Current possibilities of the use of ferritin in clinical diagnosis] 50
Treatment with short-term, high-dose cyclosporin A in children with refractory chronic idiopathic thrombocytopenic purpura 50
Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases 50
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 49
[Diagnostic methods in iron deficiency states. Comparative data on free protoporphyrins of erythrocytes in iron deficiency states and in thalassemia] 49
Serum Hepcidin and Iron Absorption in Pediatric Inflammatory Bowel Disease. 49
Long term efficacy of iron chelation therapy with deferasirox on endocrine function in thalassemia major 49
[An unusual salt-losing syndrome: pseudohypoaldosteronism. Description of a case] 48
[Problems of antibiotic therapy in pediatrics] 48
Terapia con rHu Epo in un caso di diabete mellito “early onset” ed anemia aplastica normocitica 48
Hereditary spherocytosis due to a novel frameshift mutation in AE1 cytoplasmic COOH terminal tail: band 3 Vesuvio 47
[Comparative evaluation of the activity "in vitro" of 4 aminoglycosides (gentamycin, sisomicin, tobramycin, amikacin)] 47
Le anemie diseritropoietiche 47
ROBO2 gene variants are associated with familial vesicouretral reflux 47
Rituximab for the treatment of refractory autoimmune hemolytic anemia in children 47
La prevenzione dell’anemia mediterranea in Campania: stato attuale e prospettive 47
Long-term follow-up analysis after rituximab therapy in children with refractory symptomatic ITP: identification of factors predictive of a sustained response 46
Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II) 46
Anti-CD20 monoclonal antibody for the treatment of severe, immune-mediated, pure red cell aplasia and hemolytic anemia 46
[Cartilage-hair hypoplasia: clinical and immunological study] 46
Management of acute childhood idiopathic thrombocytopenic purpura according to AIEOP consensus guidelines:assessment of Italian experience 45
Erythropoietin treatment can prevent blood transfusion in infantile pyknocytosis 45
EVALUATION OF BODY IRON STATUS IN ITALIAN CARRIERS OF BETA-THALASSEMIA TRAIT 45
Gender- and age-related distinctions for the in vivo prooxidant state in Fanconi anaemia patients 45
Bilateral neuroretinitis in a 6-year-old boy with acquired toxoplasmosis 45
[Hematological screening of a group of children from a school population] 45
[Very unusual combination: congenital nephrosis and bilateral congenital glaucoma] 45
Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis 44
Molecular heterogeneity of hereditary elliptocytosis in Italy 44
[Glycerol test in thalassemia diagnosis (author's transl)] 44
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 43
Flow-cytometric analysis of erythrocytes and reticulocytes in congenital dyserythropoietic anaemia type II (CDA II): value in differential diagnosis with hereditary spherocytosis 43
Diamond-Blackfan anaemia in the Italian population 43
[The L-dopa test in diagnosis of pituitary dwarfism] 43
Anti-CD20 monoclonal antibody (Rituximab) for life-threatening autoimmune haemolytic anaemia in a patient with systemic lupus erythematosus 43
[Prevention therapy of infections in the course of granulocytopenia] 43
Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature 42
The DMT1 IVS4+44C>A polymorphism and the risk of iron deficiency anemia in children with celiac disease 42
Reversible erythrocyte skeleton destabilization is modulated by beta-spectrin phosphorylation in childhood leukemia 41
Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotype 41
A trial of high-dose dexamethasone therapy for chronic idiopathic thrombocytopenic purpura in childhood 41
Splenectomy in children with chronic ITP: long-term efficacy and relation between its outcome and responses to previous treatments 40
[Fetal hemoglobin during the first year of life: evaluation of total erythrocytes, neocytes and gerocytes] 40
[Prenatal diagnosis: current knowledge and future prospects] 40
Membranous glomerulopathy in children given allogeneic hematopoietic stem cell transplantation 39
Totale 5.667
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Categoria #
all - tutte 25.149
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 25.149
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020558 0 0 0 0 137 33 194 54 74 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
2024/2025280 9 18 19 71 163 0 0 0 0 0 0 0
Totale 6.313