IRIS
NOBILI, Bruno
 Distribuzione geografica
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Continente #
NA - Nord America 2.796
EU - Europa 2.546
AS - Asia 388
Continente sconosciuto - Info sul continente non disponibili 5
AF - Africa 2
SA - Sud America 2
OC - Oceania 1
Totale 5.740
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Nazione #
US - Stati Uniti d'America 2.781
IE - Irlanda 783
UA - Ucraina 460
GB - Regno Unito 357
CN - Cina 277
IT - Italia 273
DE - Germania 232
SE - Svezia 151
FI - Finlandia 120
TR - Turchia 78
FR - Francia 72
GR - Grecia 68
BE - Belgio 18
CA - Canada 12
IN - India 6
IR - Iran 6
EU - Europa 5
SA - Arabia Saudita 5
NL - Olanda 4
HK - Hong Kong 3
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
BR - Brasile 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
ES - Italia 1
KR - Corea 1
PH - Filippine 1
PK - Pakistan 1
PL - Polonia 1
PT - Portogallo 1
RO - Romania 1
SG - Singapore 1
TW - Taiwan 1
Totale 5.740
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Città #
Dublin 782
Jacksonville 692
Chandler 596
Ann Arbor 125
Princeton 120
Medford 111
Boardman 103
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
Grumo Nevano 13
Hefei 13
Nanchang 13
Auburn Hills 12
Norwalk 11
Elora 9
Milan 8
Naples 8
Guangzhou 7
Hangzhou 7
Hebei 7
Shenyang 7
Tianjin 7
Helsinki 6
Houston 6
Redwood City 6
Zhengzhou 6
Lanzhou 5
Los Angeles 5
Ningbo 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
Taiyuan 3
Tehran 3
Verona 3
Alexandria 2
Altamura 2
Amsterdam 2
Bologna 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
Chandigarh 1
Chaoyang 1
Cocoa 1
Codogno 1
Collegeville 1
Cupertino 1
Dhaka 1
Edmonton 1
Ferrara 1
Totale 3.549
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Nome #
Cannabinoid receptor 2-63 QQ varianti s associated with severe necroinflammation in chronic epatiti C 106
Ematologia 105
Cannabinoid receptor 2 as anti-obesity target: inflammation, fat storage and browning modulation. 103
Association between cannabinoid receptor type 2 Q63R variant and oligo/polyarticular juvenile idiopathic arthritis 97
Cannabinoid receptor 2 Q63R variant could modulate the relationship between childhood obesity and age at menarche 83
Endocannabinoid Research Group (ERG), Italy. The endovanilloid/endocannabinoid system: a new potential target for osteoporosis therapy. 83
Iron overload enhances human mesenchymal stromal cell growth and hampers matrix calcification 77
Association Between a Polymorphism in Cannabinoid Receptor 2 and Severe Necroinflammation in Patients With Chronic Hepatitis C. 75
Endocrine function and bone disease during long-term chelation therapy with deferasirox in patients with β-thalassemia major. 70
The cannabinoid receptor type 2 as mediator of mesenchymal stromal cell immunosuppressive properties. 69
The 17-β-oestradiol inhibits osteoclast activity by increasing the cannabinoid CB2 receptor expression. 68
A case of cutaneous mastocytosis associated with A-G dysgammaglobulinemia 68
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range. 67
ERITROCITOSI CONGENITA CAUSATA DA ALTERAZIONI DEL SISTEMA SENSORE DELL’OSSIGENO 66
PKCβII-mediated cross-talk of TRPV1/CB2 modulates the glucocorticoid-induced osteoclast overactivity 66
The genetic ablation or pharmacological inhibition of TRPV1 signalling is beneficial for the restoration of quiescent osteoclast activity in ovariectomized mice. 64
The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 function 63
CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura. 63
The cannabinoid receptor type 2 Q63R variant increases the risk of celiac disease: implication for a novel molecular biomarker and future therapeutic intervention. 63
The endovanilloid/endocannabinoid system: A new potential target for osteoporosis therapy 62
Von Hippel-Lindau-dependent polycythemia is endemic on the island of Ischia: identification of a novel cluster. 62
Vitamin A and infancy. Biochemical, functional, and clinical aspects 62
Vitamin A and infancy. Biochemical, functional, and clinical aspects 61
The 17-estradiol inhibits osteoclast activity by increasing the cannabinoid CB2 receptor expression 61
Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency 60
Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele 60
CB2 and TRPV1 receptors oppositely modulate in vitro human osteoblast activity 60
EPO receptor gain-of-function causes hereditary polycythemia, alters CD34 cell differentiation and increases circulating endothelial precursors. 59
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibition 59
Iron overload causes osteoporosis in Thalassemia Major patients through interaction with TRPV1 channels. 59
[Sanfilippo's disease of type B. Study of the enzymatic deficiency in a family] 58
Studio retrospettivo sulle complicanze emato-oncologiche nella neurofibromatosi tipo 1 in età pediatrica 58
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis 57
Concordanza tra visita oculistica e RM encefalo nello screening del glioma delle vie ottiche nei pazienti pediatrici con neurofibromatosi tipo 1 57
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. 56
[Antibiotic therapy: cephalosporins] 56
Interaction between metabotropic and NMDA glutamate receptors participate in the periaqueductal grey pain modulatory system 55
Spectrum of FANCA mutations in Italian Fanconi anemia patients: identification of six novel alleles and phenotypic characterization of the S858R variant 55
Effects of nebivolol on human platelet aggregation 54
[Fluorimetric determination of erythrocytic free protoporphyrins in evaluation of iron deficiency states] 54
Rituximab (anti-CD20 monoclonal antibody) in children with chronic refractory symptomatic immune thrombocytopenic purpura: efficacy and safety of treatment 53
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience 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 51
[A case of progeria associated with Uhl's syndrome] 51
Effect of eradication of Helicobacter pylori in children with chronic immune thrombocytopenia: a prospective, controlled, multicenter study. 50
Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis 50
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 50
A modification of the 'pink test' may improve the diagnosis of hereditary spherocytosis 50
[Alpha thalassemia in Campania: results of a survey of 319 newborn infants] 50
Amoxicillin-induced hemolytic anemia in a child with glucose 6-phosphate isomerase deficiency 50
Bart's hemoglobin in newborn infants of Campania 50
Long-term efficacy of deferasirox for cardiac siderosis in thalassemia major 50
ROBO2 gene variants are associated with familial vesicoureteral reflux 49
COINHERITANCE OF GILBERT SYNDROME INCREASES THE RISK FOR DEVELOPING GALLSTONES IN PATIENTS WITH HEREDITARY SPHEROCYTOSIS 49
Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases 48
Factors influencing post-transfusional platelet increment in pediatric patients given hematopoietic stem cell transplantation 47
Treatment with short-term, high-dose cyclosporin A in children with refractory chronic idiopathic thrombocytopenic purpura 47
Long term efficacy of iron chelation therapy with deferasirox on endocrine function in thalassemia major 47
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 46
[Current possibilities of the use of ferritin in clinical diagnosis] 46
Serum Hepcidin and Iron Absorption in Pediatric Inflammatory Bowel Disease. 46
ROBO2 gene variants are associated with familial vesicouretral reflux 45
[An unusual salt-losing syndrome: pseudohypoaldosteronism. Description of a case] 45
Rituximab for the treatment of refractory autoimmune hemolytic anemia in children 45
La prevenzione dell’anemia mediterranea in Campania: stato attuale e prospettive 45
Terapia con rHu Epo in un caso di diabete mellito “early onset” ed anemia aplastica normocitica 45
Long-term follow-up analysis after rituximab therapy in children with refractory symptomatic ITP: identification of factors predictive of a sustained response 44
Hereditary spherocytosis due to a novel frameshift mutation in AE1 cytoplasmic COOH terminal tail: band 3 Vesuvio 44
[Comparative evaluation of the activity "in vitro" of 4 aminoglycosides (gentamycin, sisomicin, tobramycin, amikacin)] 44
Le anemie diseritropoietiche 44
[Diagnostic methods in iron deficiency states. Comparative data on free protoporphyrins of erythrocytes in iron deficiency states and in thalassemia] 44
[Problems of antibiotic therapy in pediatrics] 44
Management of acute childhood idiopathic thrombocytopenic purpura according to AIEOP consensus guidelines:assessment of Italian experience 43
Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II) 43
Anti-CD20 monoclonal antibody for the treatment of severe, immune-mediated, pure red cell aplasia and hemolytic anemia 43
EVALUATION OF BODY IRON STATUS IN ITALIAN CARRIERS OF BETA-THALASSEMIA TRAIT 43
Bilateral neuroretinitis in a 6-year-old boy with acquired toxoplasmosis 43
[Hematological screening of a group of children from a school population] 43
Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis 42
Gender- and age-related distinctions for the in vivo prooxidant state in Fanconi anaemia patients 42
[Cartilage-hair hypoplasia: clinical and immunological study] 42
Flow-cytometric analysis of erythrocytes and reticulocytes in congenital dyserythropoietic anaemia type II (CDA II): value in differential diagnosis with hereditary spherocytosis 41
Molecular heterogeneity of hereditary elliptocytosis in Italy 41
Anti-CD20 monoclonal antibody (Rituximab) for life-threatening autoimmune haemolytic anaemia in a patient with systemic lupus erythematosus 41
[Very unusual combination: congenital nephrosis and bilateral congenital glaucoma] 41
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 40
Erythropoietin treatment can prevent blood transfusion in infantile pyknocytosis 40
Reversible erythrocyte skeleton destabilization is modulated by beta-spectrin phosphorylation in childhood leukemia 40
Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature 40
Diamond-Blackfan anaemia in the Italian population 40
[The L-dopa test in diagnosis of pituitary dwarfism] 40
[Glycerol test in thalassemia diagnosis (author's transl)] 40
[Prevention therapy of infections in the course of granulocytopenia] 40
The DMT1 IVS4+44C>A polymorphism and the risk of iron deficiency anemia in children with celiac disease 40
Splenectomy in children with chronic ITP: long-term efficacy and relation between its outcome and responses to previous treatments 39
Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotype 39
A trial of high-dose dexamethasone therapy for chronic idiopathic thrombocytopenic purpura in childhood 39
Successful umbilical cord blood transplantation in a child with dyskeratosis congenita after a fludarabine-based reduced-intensity conditioning regimen 37
[Fetal hemoglobin during the first year of life: evaluation of total erythrocytes, neocytes and gerocytes] 37
[Prenatal diagnosis: current knowledge and future prospects] 37
Totale 5.339
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Categoria #
all - tutte 19.608
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 19.608
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201919 0 0 0 0 0 0 0 0 0 0 7 12
2019/2020859 149 123 20 9 137 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
2023/2024439 69 14 22 65 196 29 15 25 4 0 0 0
Totale 5.935