Bicocca Open Archive

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MARIANI, RAFFAELLA
 Distribuzione geografica
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Continente #
NA - Nord America 8.053
AS - Asia 3.588
EU - Europa 3.297
SA - Sud America 586
AF - Africa 78
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 3
Totale 15.614
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Nazione #
US - Stati Uniti d'America 7.601
SG - Singapore 1.331
CN - Cina 894
DE - Germania 529
IT - Italia 524
BR - Brasile 441
RU - Federazione Russa 437
HK - Hong Kong 432
SE - Svezia 430
CA - Canada 400
VN - Vietnam 362
IE - Irlanda 304
UA - Ucraina 255
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 55
BE - Belgio 43
IQ - Iraq 41
NL - Olanda 41
DK - Danimarca 39
PK - Pakistan 33
MX - Messico 32
JP - Giappone 26
CO - Colombia 25
ES - Italia 25
ID - Indonesia 25
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
RO - Romania 10
EG - Egitto 9
MA - Marocco 9
MY - Malesia 9
PY - Paraguay 9
AU - Australia 8
CL - Cile 8
ET - Etiopia 8
KE - Kenya 8
AE - Emirati Arabi Uniti 7
NP - Nepal 7
PE - Perù 7
BO - Bolivia 6
TN - Tunisia 6
CH - Svizzera 5
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
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
GT - Guatemala 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
GY - Guiana 1
IM - Isola di Man 1
IS - Islanda 1
Totale 15.594
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Città #
Ann Arbor 1.283
Singapore 809
Ashburn 754
Woodbridge 582
Fairfield 447
Hong Kong 419
Houston 419
San Jose 406
Chandler 394
Dublin 297
Toronto 287
Frankfurt am Main 273
Jacksonville 270
Wilmington 260
New York 200
Dearborn 198
Seattle 167
Milan 160
Cambridge 158
Beijing 151
Santa Clara 127
Los Angeles 119
Princeton 109
Ho Chi Minh City 101
Chicago 96
Nanjing 96
The Dalles 90
Hanoi 84
Vienna 81
Hefei 76
Boardman 63
Shanghai 62
Buffalo 58
Seoul 57
Council Bluffs 52
Rome 52
Dallas 51
Lawrence 49
Lauterbourg 48
São Paulo 47
Lachine 45
Altamura 44
Munich 44
Brussels 38
Helsinki 38
Moscow 35
San Diego 35
Nanchang 29
Orem 28
Dong Ket 26
Turku 25
Ottawa 24
Shenyang 23
Turin 23
Changsha 22
Chennai 20
Hebei 19
London 19
Zhengzhou 19
Jinan 18
Guangzhou 17
Rio de Janeiro 17
Andover 16
Tampa 15
Tokyo 15
Boston 14
Da Nang 14
Jiaxing 14
Tashkent 14
Tianjin 14
Dhaka 13
Haiphong 13
Jakarta 13
Montreal 13
Philadelphia 13
Atlanta 12
Belo Horizonte 12
Columbus 12
Indianapolis 12
Ningbo 12
Baghdad 11
Brasília 11
Brooklyn 11
Huizen 11
Phoenix 11
Denver 10
Lahore 10
Mexico City 10
Auburn Hills 9
Campinas 9
Nuremberg 9
Fremont 8
Hangzhou 8
Istanbul 8
Jeddah 8
Johannesburg 8
Karachi 8
Kocaeli 8
Mountain View 8
Mumbai 8
Totale 10.485
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Nome #
Hepcidin regulation in a mouse model of acute hypoxia 592
Phenotypic heterogeneity in seven Italian cases of aceruloplasminemia 446
GNPAT rs11558492 is not a major modifier of iron status: Study of Italian hemochromatosis patients and blood donors 410
Serum ferritin and liver features in a cohort of 15 patients affected by Gaucher disease 408
Re-evaluation of clinical and histological criteria for diagnosis of dysmetabolic iron overload syndrome 385
A severe hemojuvelin mutation leading to late onset of HFE2-hemochromatosis 383
Hif1a: A putative modifier of hemochromatosis 382
Prolonged exposure to welding fumes as a novel cause of systemic iron overload 349
Inherited iron overload disorders 346
Type 3 hemochromatosis and beta-thalassemia trait 341
Expression of hepcidin and other iron-related genes in type 3 hemochromatosis due to a novel mutation in transferrin receptor-2 336
Genetic and metabolic factors are associated with increased hepatic iron stores in a selected population of p.Cys282Tyr heterozygotes 336
Hepcidin regulation in a mouse model of acute hypoxia 336
Transferrin receptor 2 mutations in patients with juvenile hemochromatosis phenotype 331
Novel mutations of the ferroportin gene (SLC40A1): Analysis of 56 consecutive patients with unexplained iron overload 329
The presence of two or more metabolic alterations and hepatic steatosis characterizes the dysmetabolic iron overload syndrome 329
Unexplained isolated hyperferritinemia without iron overload 324
Alterations in sympathetic nerve traffic in genetic haemochromatosis before and after iron depletion therapy: A microneurographic study 321
Hepcidin and iron-related gene expression in subjects with Dysmetabolic Hepatic Iron Overload 301
Heterogeneity of iron overload: Clinical, biochemical, histopathologic and genetic study of 70 patients 298
CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients 295
Dysmetabolic Hepatic Iron Overload Syndrome: Analysis of Hepcidin Response to Acute Oral Iron and Chronic Iron Overload 294
Proprotein convertase 7 rs236918 associated with liver fibrosis in Italian patients with HFE-related hemochromatosis 294
Prevalence of HFE mutations in upper northern Italy: study of 1132 unrelated blood donors 293
Does aceruloplasminemia modulate iron phenotype in thalassemia intermedia? 290
Iron Overload Increases Sympathetic Nervous Activity: Study in Hemochromatosis Patients at Diagnosis and Iron Depletion 281
Hepcidin expression in iron overload diseases is variably modulated by circulating factors 280
Increased serum ferritin is common in men with essential hypertension 276
UNEXPLAINED ISOLATED HYPERFERRITINEMIA IN PATIENTS WITHOUT MUTATIONS IN FERRITIN GENE AND L-FERRITIN IRES REGIONS 272
HFE and SLC40A1 polymorphisms in patients with unexplained iron overload 269
Identification of novel mutations by targeted NGS panel in patients with hyperferritinemia 265
Effects of plasma transfusion on hepcidin production in human congenital hypotransferrinemia 262
Prevalence of C282Y and E168X HFE mutations in an italian population of northern european ancestry 260
Il sovraccarico di ferro: modulatore della risposta adrenergica 260
Reduced expression of hepcidin in patients with myelodysplastic syndrome and myelofibrosis: The causes might be more heterogeneous than in thalassaemia 259
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 253
Analysis of Polymorphisms of Genes Regulating Hepcidin Transcription in Hfe-Hemochromatosis 251
GNPAT rs11558492 is not associated to iron overload in Italian HFE p.C282Y homozygotes 245
Haemochromatosis in patients with β-thalassaemia trait 238
Homozygous deletion of HFE: The Sardinian hemochromatosis? 238
Natural history of juvenile haemochromatosis 232
Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation 225
Reduced Insulin Sensitivity is Associated with Adrenergic Overdrive Independently on Obesity and Hypertension 221
Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosis 216
Homozygosity for transferrin receptor-2 y250x mutation induces early iron overload 214
Iron accumulation in chronic hepatitis C: relation of hepatic iron distribution, HFE genotype, and disease course 213
Reference Values of Ceruloplasmin across the Adult Age Range in a Large Italian Healthy Population 212
Hepcidin modulation in human diseases: From research to clinic 201
Iron metabolism in thalassemia and sickle cell disease 201
Erythrocytapheresis plus erythropoietin: An alternative therapy for selected patients with hemochromatosis and severe organ damage 199
Interaction Between the PNPLA3 I148M Mutation, Body Weight, And Steatosis, In Determining The Progression To Cirrhosis In Hereditary Hemochromatosis 196
Reduced insulin sensitivity is associated with adrenergic overdrive in hemochromatosis independently on obesity and hypertension 196
MR imaging of cerebral cortical involvement in aceruloplasminemia 188
Hereditary Hyperferritinemia 188
GH deficiency in adult B-thalassemia major patients and its relationship with IGF-1 production 186
Interaction between the PNPLA3 I148M mutation and body weight in determining steatosis and the progression to cirrhosis in hereditary hemochromatosis 163
Totale 15.909
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Categoria #
all - tutte 48.755
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 48.755
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202198 0 0 0 0 0 0 0 0 0 0 0 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
2025/20265.444 541 240 384 524 688 306 793 238 490 488 418 334
Totale 15.909