Bicocca Open Archive

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MARIANI, RAFFAELLA
 Distribuzione geografica
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Continente #
NA - Nord America 6.668
EU - Europa 2.883
AS - Asia 2.597
SA - Sud America 453
AF - Africa 40
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 3
Totale 12.648
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Nazione #
US - Stati Uniti d'America 6.533
SG - Singapore 998
CN - Cina 808
DE - Germania 520
RU - Federazione Russa 431
SE - Svezia 429
BR - Brasile 380
HK - Hong Kong 345
IE - Irlanda 300
IT - Italia 294
UA - Ucraina 251
GB - Regno Unito 205
VN - Vietnam 164
CA - Canada 111
FI - Finlandia 100
AT - Austria 90
FR - Francia 86
IN - India 54
KR - Corea 48
TR - Turchia 45
BE - Belgio 41
DK - Danimarca 36
NL - Olanda 35
AR - Argentina 32
BD - Bangladesh 20
JP - Giappone 20
MX - Messico 17
ID - Indonesia 16
IQ - Iraq 16
ZA - Sudafrica 16
PL - Polonia 11
IR - Iran 10
LT - Lituania 10
PK - Pakistan 10
CO - Colombia 9
EC - Ecuador 9
SA - Arabia Saudita 9
PY - Paraguay 7
RO - Romania 7
ES - Italia 6
UZ - Uzbekistan 6
CZ - Repubblica Ceca 5
EG - Egitto 5
KE - Kenya 5
PE - Perù 5
VE - Venezuela 5
AU - Australia 4
CL - Cile 4
MY - Malesia 4
AE - Emirati Arabi Uniti 3
BA - Bosnia-Erzegovina 3
BG - Bulgaria 3
DO - Repubblica Dominicana 3
DZ - Algeria 3
HR - Croazia 3
IL - Israele 3
MA - Marocco 3
CH - Svizzera 2
EU - Europa 2
GR - Grecia 2
NG - Nigeria 2
NO - Norvegia 2
NP - Nepal 2
OM - Oman 2
SC - Seychelles 2
TN - Tunisia 2
TW - Taiwan 2
AL - Albania 1
AM - Armenia 1
AZ - Azerbaigian 1
BB - Barbados 1
BO - Bolivia 1
BY - Bielorussia 1
CG - Congo 1
GE - Georgia 1
HU - Ungheria 1
IM - Isola di Man 1
IS - Islanda 1
JM - Giamaica 1
JO - Giordania 1
KG - Kirghizistan 1
KW - Kuwait 1
KZ - Kazakistan 1
LB - Libano 1
LK - Sri Lanka 1
LV - Lettonia 1
MD - Moldavia 1
MK - Macedonia 1
MT - Malta 1
PH - Filippine 1
PT - Portogallo 1
QA - Qatar 1
RS - Serbia 1
SV - El Salvador 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
XK - ???statistics.table.value.countryCode.XK??? 1
ZM - Zambia 1
Totale 12.648
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Città #
Ann Arbor 1.283
Singapore 615
Woodbridge 582
Ashburn 578
Fairfield 447
Houston 418
Chandler 394
Hong Kong 343
Dublin 294
Jacksonville 270
Frankfurt am Main 268
Wilmington 260
Dearborn 198
New York 176
Seattle 165
Cambridge 158
Beijing 147
Santa Clara 113
Princeton 109
Nanjing 96
Los Angeles 85
Vienna 80
Milan 77
Hefei 76
Shanghai 59
Lawrence 49
Buffalo 47
Dallas 45
Ho Chi Minh City 45
Lachine 45
Altamura 44
Munich 44
Seoul 41
São Paulo 40
The Dalles 40
Brussels 36
Moscow 35
Chicago 34
San Diego 34
Boardman 30
Hanoi 30
Nanchang 29
Dong Ket 26
Helsinki 25
Turku 25
Council Bluffs 24
Ottawa 24
Shenyang 23
Changsha 22
Hebei 19
Rome 18
Zhengzhou 18
Jinan 17
Andover 16
Guangzhou 16
London 16
Rio de Janeiro 16
Turin 15
Jiaxing 14
Boston 13
Tianjin 13
Indianapolis 12
Ningbo 12
Philadelphia 12
Huizen 11
Jakarta 11
Tokyo 11
Toronto 11
Columbus 10
Denver 10
Montreal 10
Phoenix 10
Auburn Hills 9
Belo Horizonte 9
Brooklyn 9
Campinas 9
Chennai 9
Orem 9
Tampa 9
Fremont 8
Kocaeli 8
Mexico City 8
Mountain View 8
Pune 8
Salt Lake City 8
Atlanta 7
Brasília 7
Hangzhou 7
Johannesburg 7
Kunming 7
Norwalk 7
Nuremberg 7
Stockholm 7
Curitiba 6
Da Nang 6
Dhaka 6
Edmonton 6
Elk Grove Village 6
Falls Church 6
Lissone 6
Totale 8.648
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Nome #
Hepcidin regulation in a mouse model of acute hypoxia 515
Phenotypic heterogeneity in seven Italian cases of aceruloplasminemia 378
GNPAT rs11558492 is not a major modifier of iron status: Study of Italian hemochromatosis patients and blood donors 359
Serum ferritin and liver features in a cohort of 15 patients affected by Gaucher disease 353
A severe hemojuvelin mutation leading to late onset of HFE2-hemochromatosis 332
Re-evaluation of clinical and histological criteria for diagnosis of dysmetabolic iron overload syndrome 329
Hif1a: A putative modifier of hemochromatosis 319
Inherited iron overload disorders 295
Prolonged exposure to welding fumes as a novel cause of systemic iron overload 286
Genetic and metabolic factors are associated with increased hepatic iron stores in a selected population of p.Cys282Tyr heterozygotes 281
Expression of hepcidin and other iron-related genes in type 3 hemochromatosis due to a novel mutation in transferrin receptor-2 276
Transferrin receptor 2 mutations in patients with juvenile hemochromatosis phenotype 275
Novel mutations of the ferroportin gene (SLC40A1): Analysis of 56 consecutive patients with unexplained iron overload 274
Hepcidin regulation in a mouse model of acute hypoxia 271
The presence of two or more metabolic alterations and hepatic steatosis characterizes the dysmetabolic iron overload syndrome 269
Type 3 hemochromatosis and beta-thalassemia trait 267
Alterations in sympathetic nerve traffic in genetic haemochromatosis before and after iron depletion therapy: A microneurographic study 264
Unexplained isolated hyperferritinemia without iron overload 259
Hepcidin and iron-related gene expression in subjects with Dysmetabolic Hepatic Iron Overload 258
Does aceruloplasminemia modulate iron phenotype in thalassemia intermedia? 247
CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients 245
Heterogeneity of iron overload: Clinical, biochemical, histopathologic and genetic study of 70 patients 235
Hepcidin expression in iron overload diseases is variably modulated by circulating factors 234
Iron Overload Increases Sympathetic Nervous Activity: Study in Hemochromatosis Patients at Diagnosis and Iron Depletion 234
Dysmetabolic Hepatic Iron Overload Syndrome: Analysis of Hepcidin Response to Acute Oral Iron and Chronic Iron Overload 231
Prevalence of HFE mutations in upper northern Italy: study of 1132 unrelated blood donors 226
Proprotein convertase 7 rs236918 associated with liver fibrosis in Italian patients with HFE-related hemochromatosis 223
Reduced expression of hepcidin in patients with myelodysplastic syndrome and myelofibrosis: the causes might be more heterogeneous than in thalassaemia. 222
Increased serum ferritin is common in men with essential hypertension 221
Effects of plasma transfusion on hepcidin production in human congenital hypotransferrinemia 217
UNEXPLAINED ISOLATED HYPERFERRITINEMIA IN PATIENTS WITHOUT MUTATIONS IN FERRITIN GENE AND L-FERRITIN IRES REGIONS 216
HFE and SLC40A1 polymorphisms in patients with unexplained iron overload 209
Identification of novel mutations by targeted NGS panel in patients with hyperferritinemia 205
Prevalence of C282Y and E168X HFE mutations in an italian population of northern european ancestry 203
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 202
Homozygous deletion of HFE: The Sardinian hemochromatosis? 201
Analysis of Polymorphisms of Genes Regulating Hepcidin Transcription in Hfe-Hemochromatosis 200
GNPAT rs11558492 is not associated to iron overload in Italian HFE p.C282Y homozygotes 188
Reduced Insulin Sensitivity is Associated with Adrenergic Overdrive Independently on Obesity and Hypertension 187
Il sovraccarico di ferro: modulatore della risposta adrenergica 184
Natural history of juvenile haemochromatosis 182
Haemochromatosis in patients with β-thalassaemia trait 180
Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosis 178
Iron accumulation in chronic hepatitis C: relation of hepatic iron distribution, HFE genotype, and disease course 177
Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation 177
Homozygosity for transferrin receptor-2 y250x mutation induces early iron overload 172
Iron metabolism in thalassemia and sickle cell disease 170
Erythrocytapheresis plus erythropoietin: An alternative therapy for selected patients with hemochromatosis and severe organ damage 165
Reduced insulin sensitivity is associated with adrenergic overdrive in hemochromatosis independently on obesity and hypertension 163
MR imaging of cerebral cortical involvement in aceruloplasminemia 162
Hepcidin modulation in human diseases: From research to clinic 153
GH deficiency in adult B-thalassemia major patients and its relationship with IGF-1 production 152
Interaction Between the PNPLA3 I148M Mutation, Body Weight, And Steatosis, In Determining The Progression To Cirrhosis In Hereditary Hemochromatosis 147
Reference Values of Ceruloplasmin across the Adult Age Range in a Large Italian Healthy Population 128
Interaction between the PNPLA3 I148M mutation and body weight in determining steatosis and the progression to cirrhosis in hereditary hemochromatosis 125
Hereditary Hyperferritinemia 122
Totale 12.943
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Categoria #
all - tutte 42.084
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 42.084
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021629 0 0 0 0 0 73 93 66 90 146 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
2025/20262.478 541 240 384 524 688 101 0 0 0 0 0 0
Totale 12.943