Bicocca Open Archive

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MARIANI, RAFFAELLA
 Distribuzione geografica
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Continente #
NA - Nord America 7.709
AS - Asia 3.571
EU - Europa 3.098
SA - Sud America 585
AF - Africa 78
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 3
Totale 15.053
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Nazione #
US - Stati Uniti d'America 7.439
SG - Singapore 1.331
CN - Cina 892
DE - Germania 529
BR - Brasile 441
RU - Federazione Russa 437
HK - Hong Kong 432
SE - Svezia 430
VN - Vietnam 355
IT - Italia 330
IE - Irlanda 304
UA - Ucraina 255
CA - Canada 220
GB - Regno Unito 220
FR - Francia 159
IN - India 125
FI - Finlandia 113
AT - Austria 92
KR - Corea 65
TR - Turchia 59
AR - Argentina 57
BD - Bangladesh 49
BE - Belgio 43
IQ - Iraq 41
NL - Olanda 41
DK - Danimarca 39
PK - Pakistan 33
MX - Messico 32
JP - Giappone 26
CO - Colombia 25
ID - Indonesia 24
ES - Italia 23
PH - Filippine 22
SA - Arabia Saudita 20
ZA - Sudafrica 20
UZ - Uzbekistan 18
PL - Polonia 17
VE - Venezuela 16
EC - Ecuador 13
LT - Lituania 13
IR - Iran 10
EG - Egitto 9
MA - Marocco 9
PY - Paraguay 9
RO - Romania 9
AU - Australia 8
CL - Cile 8
ET - Etiopia 8
KE - Kenya 8
MY - Malesia 8
AE - Emirati Arabi Uniti 7
NP - Nepal 7
BO - Bolivia 6
PE - Perù 6
TN - Tunisia 6
CZ - Repubblica Ceca 5
DO - Repubblica Dominicana 5
HU - Ungheria 5
JO - Giordania 5
KZ - Kazakistan 5
OM - Oman 5
TH - Thailandia 5
BA - Bosnia-Erzegovina 4
BG - Bulgaria 4
DZ - Algeria 4
AZ - Azerbaigian 3
CH - Svizzera 3
HR - Croazia 3
IL - Israele 3
JM - Giamaica 3
KG - Kirghizistan 3
NG - Nigeria 3
PA - Panama 3
TW - Taiwan 3
UY - Uruguay 3
AM - Armenia 2
CR - Costa Rica 2
EU - Europa 2
GE - Georgia 2
GR - Grecia 2
MD - Moldavia 2
MT - Malta 2
NO - Norvegia 2
PS - Palestinian Territory 2
PT - Portogallo 2
RS - Serbia 2
SC - Seychelles 2
SV - El Salvador 2
TG - Togo 2
AL - Albania 1
BB - Barbados 1
BH - Bahrain 1
BW - Botswana 1
BY - Bielorussia 1
CG - Congo 1
GH - Ghana 1
GT - Guatemala 1
GY - Guiana 1
IM - Isola di Man 1
IS - Islanda 1
Totale 15.034
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Città #
Ann Arbor 1.283
Singapore 809
Ashburn 736
Woodbridge 582
Fairfield 447
Hong Kong 419
Houston 419
Chandler 394
San Jose 379
Dublin 297
Frankfurt am Main 273
Jacksonville 270
Wilmington 260
New York 199
Dearborn 198
Seattle 165
Cambridge 158
Beijing 150
Santa Clara 123
Los Angeles 114
Toronto 112
Princeton 109
Ho Chi Minh City 101
Nanjing 96
Chicago 95
The Dalles 90
Hanoi 82
Milan 81
Vienna 81
Hefei 76
Shanghai 62
Seoul 57
Buffalo 53
Dallas 50
Lawrence 49
Lauterbourg 48
São Paulo 47
Lachine 45
Altamura 44
Munich 44
Council Bluffs 41
Brussels 38
Helsinki 38
Boardman 37
Moscow 35
San Diego 34
Nanchang 29
Orem 27
Dong Ket 26
Turku 25
Ottawa 24
Rome 23
Shenyang 23
Changsha 22
Chennai 20
Hebei 19
London 19
Zhengzhou 19
Jinan 18
Guangzhou 17
Rio de Janeiro 17
Andover 16
Turin 16
Tokyo 15
Boston 14
Da Nang 14
Jiaxing 14
Tashkent 14
Tianjin 14
Dhaka 13
Philadelphia 13
Belo Horizonte 12
Indianapolis 12
Jakarta 12
Montreal 12
Ningbo 12
Atlanta 11
Baghdad 11
Brasília 11
Brooklyn 11
Haiphong 11
Huizen 11
Phoenix 11
Columbus 10
Denver 10
Lahore 10
Mexico City 10
Auburn Hills 9
Campinas 9
Nuremberg 9
Tampa 9
Fremont 8
Istanbul 8
Jeddah 8
Johannesburg 8
Karachi 8
Kocaeli 8
Mountain View 8
Mumbai 8
Paris 8
Totale 10.076
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Nome #
Hepcidin regulation in a mouse model of acute hypoxia 584
Phenotypic heterogeneity in seven Italian cases of aceruloplasminemia 431
GNPAT rs11558492 is not a major modifier of iron status: Study of Italian hemochromatosis patients and blood donors 404
Serum ferritin and liver features in a cohort of 15 patients affected by Gaucher disease 395
Re-evaluation of clinical and histological criteria for diagnosis of dysmetabolic iron overload syndrome 378
Hif1a: A putative modifier of hemochromatosis 378
A severe hemojuvelin mutation leading to late onset of HFE2-hemochromatosis 375
Inherited iron overload disorders 338
Prolonged exposure to welding fumes as a novel cause of systemic iron overload 333
Type 3 hemochromatosis and beta-thalassemia trait 330
Expression of hepcidin and other iron-related genes in type 3 hemochromatosis due to a novel mutation in transferrin receptor-2 325
Genetic and metabolic factors are associated with increased hepatic iron stores in a selected population of p.Cys282Tyr heterozygotes 324
The presence of two or more metabolic alterations and hepatic steatosis characterizes the dysmetabolic iron overload syndrome 323
Hepcidin regulation in a mouse model of acute hypoxia 322
Transferrin receptor 2 mutations in patients with juvenile hemochromatosis phenotype 321
Novel mutations of the ferroportin gene (SLC40A1): Analysis of 56 consecutive patients with unexplained iron overload 313
Unexplained isolated hyperferritinemia without iron overload 310
Alterations in sympathetic nerve traffic in genetic haemochromatosis before and after iron depletion therapy: A microneurographic study 308
Hepcidin and iron-related gene expression in subjects with Dysmetabolic Hepatic Iron Overload 294
CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients 292
Heterogeneity of iron overload: Clinical, biochemical, histopathologic and genetic study of 70 patients 289
Dysmetabolic Hepatic Iron Overload Syndrome: Analysis of Hepcidin Response to Acute Oral Iron and Chronic Iron Overload 285
Does aceruloplasminemia modulate iron phenotype in thalassemia intermedia? 284
Proprotein convertase 7 rs236918 associated with liver fibrosis in Italian patients with HFE-related hemochromatosis 284
Prevalence of HFE mutations in upper northern Italy: study of 1132 unrelated blood donors 281
Hepcidin expression in iron overload diseases is variably modulated by circulating factors 272
Iron Overload Increases Sympathetic Nervous Activity: Study in Hemochromatosis Patients at Diagnosis and Iron Depletion 270
Increased serum ferritin is common in men with essential hypertension 269
Identification of novel mutations by targeted NGS panel in patients with hyperferritinemia 260
HFE and SLC40A1 polymorphisms in patients with unexplained iron overload 258
UNEXPLAINED ISOLATED HYPERFERRITINEMIA IN PATIENTS WITHOUT MUTATIONS IN FERRITIN GENE AND L-FERRITIN IRES REGIONS 255
Reduced expression of hepcidin in patients with myelodysplastic syndrome and myelofibrosis: The causes might be more heterogeneous than in thalassaemia 250
Il sovraccarico di ferro: modulatore della risposta adrenergica 248
Effects of plasma transfusion on hepcidin production in human congenital hypotransferrinemia 246
Prevalence of C282Y and E168X HFE mutations in an italian population of northern european ancestry 244
GNPAT rs11558492 is not associated to iron overload in Italian HFE p.C282Y homozygotes 236
Analysis of Polymorphisms of Genes Regulating Hepcidin Transcription in Hfe-Hemochromatosis 236
The iron-hypoxia link: hepcidin has a central role in the response to acute and chronic exposure to hypobaric hypoxia. data from the highcare project 236
Homozygous deletion of HFE: The Sardinian hemochromatosis? 232
Haemochromatosis in patients with β-thalassaemia trait 228
Natural history of juvenile haemochromatosis 219
Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation 215
Reduced Insulin Sensitivity is Associated with Adrenergic Overdrive Independently on Obesity and Hypertension 212
Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosis 210
Iron accumulation in chronic hepatitis C: relation of hepatic iron distribution, HFE genotype, and disease course 207
Reference Values of Ceruloplasmin across the Adult Age Range in a Large Italian Healthy Population 200
Homozygosity for transferrin receptor-2 y250x mutation induces early iron overload 198
Iron metabolism in thalassemia and sickle cell disease 196
Hepcidin modulation in human diseases: From research to clinic 191
Erythrocytapheresis plus erythropoietin: An alternative therapy for selected patients with hemochromatosis and severe organ damage 190
Reduced insulin sensitivity is associated with adrenergic overdrive in hemochromatosis independently on obesity and hypertension 189
GH deficiency in adult B-thalassemia major patients and its relationship with IGF-1 production 184
MR imaging of cerebral cortical involvement in aceruloplasminemia 183
Interaction Between the PNPLA3 I148M Mutation, Body Weight, And Steatosis, In Determining The Progression To Cirrhosis In Hereditary Hemochromatosis 181
Hereditary Hyperferritinemia 181
Interaction between the PNPLA3 I148M mutation and body weight in determining steatosis and the progression to cirrhosis in hereditary hemochromatosis 151
Totale 15.348
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Categoria #
all - tutte 46.763
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 46.763
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021161 0 0 0 0 0 0 0 0 0 0 63 98
2021/2022878 53 104 101 65 56 50 43 34 40 74 79 179
2022/20231.484 212 433 140 150 96 209 9 80 89 9 43 14
2023/2024882 38 42 42 32 95 252 173 59 36 9 7 97
2024/20251.919 94 190 103 84 200 69 96 123 199 309 167 285
2025/20264.883 541 240 384 524 688 306 793 238 490 488 191 0
Totale 15.348