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MARIANI, RAFFAELLA
 Distribuzione geografica
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Continente #
NA - Nord America 5.751
EU - Europa 2.643
AS - Asia 1.193
SA - Sud America 152
AF - Africa 23
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 3
Totale 9.770
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Nazione #
US - Stati Uniti d'America 5.659
DE - Germania 476
SG - Singapore 460
CN - Cina 446
SE - Svezia 423
RU - Federazione Russa 378
IE - Irlanda 300
IT - Italia 271
UA - Ucraina 250
GB - Regno Unito 178
BR - Brasile 138
HK - Hong Kong 116
CA - Canada 88
AT - Austria 80
FI - Finlandia 73
FR - Francia 62
BE - Belgio 41
TR - Turchia 37
DK - Danimarca 36
VN - Vietnam 35
IN - India 34
NL - Olanda 32
ID - Indonesia 11
JP - Giappone 10
IR - Iran 9
KR - Corea 7
RO - Romania 7
PK - Pakistan 6
CZ - Repubblica Ceca 5
ZA - Sudafrica 5
AR - Argentina 4
AU - Australia 4
LT - Lituania 4
PL - Polonia 4
UZ - Uzbekistan 4
BG - Bulgaria 3
DZ - Algeria 3
EC - Ecuador 3
EG - Egitto 3
KE - Kenya 3
MY - Malesia 3
AE - Emirati Arabi Uniti 2
BA - Bosnia-Erzegovina 2
CH - Svizzera 2
CL - Cile 2
CO - Colombia 2
EU - Europa 2
GR - Grecia 2
HR - Croazia 2
MA - Marocco 2
MD - Moldavia 2
MX - Messico 2
NG - Nigeria 2
NO - Norvegia 2
SC - Seychelles 2
TW - Taiwan 2
AL - Albania 1
AM - Armenia 1
AZ - Azerbaigian 1
BO - Bolivia 1
CG - Congo 1
ES - Italia 1
GE - Georgia 1
HU - Ungheria 1
IM - Isola di Man 1
IQ - Iraq 1
IS - Islanda 1
JM - Giamaica 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LK - Sri Lanka 1
LV - Lettonia 1
MK - Macedonia 1
MT - Malta 1
NZ - Nuova Zelanda 1
OM - Oman 1
PE - Perù 1
PH - Filippine 1
SA - Arabia Saudita 1
SV - El Salvador 1
TH - Thailandia 1
TN - Tunisia 1
VE - Venezuela 1
XK - ???statistics.table.value.countryCode.XK??? 1
ZM - Zambia 1
Totale 9.770
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Città #
Ann Arbor 1.283
Woodbridge 582
Fairfield 447
Houston 412
Chandler 394
Singapore 309
Dublin 294
Ashburn 280
Jacksonville 268
Frankfurt am Main 259
Wilmington 258
Dearborn 198
Seattle 164
Cambridge 158
New York 145
Hong Kong 114
Princeton 109
Santa Clara 108
Nanjing 96
Vienna 75
Milan 71
Shanghai 59
Lawrence 49
Lachine 45
Altamura 44
Beijing 43
Brussels 36
San Diego 34
Boardman 30
Nanchang 29
Dong Ket 26
Council Bluffs 24
Ottawa 24
Helsinki 23
Shenyang 23
Changsha 20
Hebei 19
Los Angeles 17
Andover 16
Moscow 16
Zhengzhou 16
Jinan 15
Turin 15
Jiaxing 14
Rome 13
Guangzhou 12
Ningbo 12
Huizen 11
Munich 11
Tianjin 11
Jakarta 10
Philadelphia 10
São Paulo 10
Auburn Hills 9
Toronto 9
Fremont 8
Kocaeli 8
London 8
Mountain View 8
Pune 8
Belo Horizonte 7
Norwalk 7
Edmonton 6
Falls Church 6
Hangzhou 6
Kunming 6
Lissone 6
Phoenix 6
Segrate 6
Hefei 5
Nuremberg 5
Rio de Janeiro 5
Sacramento 5
Washington 5
Cagliari 4
Chicago 4
Düsseldorf 4
Lanzhou 4
Monmouth Junction 4
Redmond 4
San Francisco 4
Taizhou 4
Waanrode 4
Agropoli 3
Bengaluru 3
Brasília 3
Chongqing 3
Daejeon 3
Dallas 3
Kiev 3
Ladera Ranch 3
Laurel 3
Lecco 3
Nairobi 3
Paris 3
Quito 3
Saint Petersburg 3
San Mateo 3
Sydney 3
Tashkent 3
Totale 6.987
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Nome #
Hepcidin regulation in a mouse model of acute hypoxia 411
Phenotypic heterogeneity in seven Italian cases of aceruloplasminemia 318
GNPAT rs11558492 is not a major modifier of iron status: Study of Italian hemochromatosis patients and blood donors 304
Serum ferritin and liver features in a cohort of 15 patients affected by Gaucher disease 292
A severe hemojuvelin mutation leading to late onset of HFE2-hemochromatosis 275
Re-evaluation of clinical and histological criteria for diagnosis of dysmetabolic iron overload syndrome 254
Hif1a: A putative modifier of hemochromatosis 237
Inherited iron overload disorders 234
Hepcidin regulation in a mouse model of acute hypoxia 222
Genetic and metabolic factors are associated with increased hepatic iron stores in a selected population of p.Cys282Tyr heterozygotes 216
Hepcidin and iron-related gene expression in subjects with Dysmetabolic Hepatic Iron Overload 213
Type 3 hemochromatosis and beta-thalassemia trait 211
The presence of two or more metabolic alterations and hepatic steatosis characterizes the dysmetabolic iron overload syndrome 211
Transferrin receptor 2 mutations in patients with juvenile hemochromatosis phenotype 210
Expression of hepcidin and other iron-related genes in type 3 hemochromatosis due to a novel mutation in transferrin receptor-2. 208
Does aceruloplasminemia modulate iron phenotype in thalassemia intermedia? 203
Unexplained isolated hyperferritinemia without iron overload 200
Prolonged exposure to welding fumes as a novel cause of systemic iron overload 199
Alterations in sympathetic nerve traffic in genetic haemochromatosis before and after iron depletion therapy: A microneurographic study 195
Reduced expression of hepcidin in patients with myelodysplastic syndrome and myelofibrosis: the causes might be more heterogeneous than in thalassaemia. 194
Iron Overload Increases Sympathetic Nervous Activity: Study in Hemochromatosis Patients at Diagnosis and Iron Depletion 192
Novel mutations of the ferroportin gene (SLC40A1): Analysis of 56 consecutive patients with unexplained iron overload 191
Effects of plasma transfusion on hepcidin production in human congenital hypotransferrinemia 182
CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients 177
Dysmetabolic Hepatic Iron Overload Syndrome: Analysis of Hepcidin Response to Acute Oral Iron and Chronic Iron Overload 177
Heterogeneity of iron overload: Clinical, biochemical, histopathologic and genetic study of 70 patients 175
Hepcidin expression in iron overload diseases is variably modulated by circulating factors 174
Prevalence of HFE mutations in upper northern Italy: study of 1132 unrelated blood donors 173
Proprotein convertase 7 rs236918 associated with liver fibrosis in Italian patients with HFE-related hemochromatosis 171
Homozygous deletion of HFE: The Sardinian hemochromatosis? 169
Increased serum ferritin is common in men with essential hypertension 156
UNEXPLAINED ISOLATED HYPERFERRITINEMIA IN PATIENTS WITHOUT MUTATIONS IN FERRITIN GENE AND L-FERRITIN IRES REGIONS 156
Analysis of Polymorphisms of Genes Regulating Hepcidin Transcription in Hfe-Hemochromatosis 156
HFE and SLC40A1 polymorphisms in patients with unexplained iron overload 155
Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation 153
Reduced Insulin Sensitivity is Associated with Adrenergic Overdrive Independently on Obesity and Hypertension 152
Prevalence of C282Y and E168X HFE mutations in an italian population of northern european ancestry 148
Natural history of juvenile haemochromatosis 148
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 147
Haemochromatosis in patients with β-thalassaemia trait 146
Il sovraccarico di ferro: modulatore della risposta adrenergica 144
Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosis 143
GNPAT rs11558492 is not associated to iron overload in Italian HFE p.C282Y homozygotes 142
Iron accumulation in chronic hepatitis C: relation of hepatic iron distribution, HFE genotype, and disease course 140
Homozygosity for transferrin receptor-2 y250x mutation induces early iron overload 139
Iron metabolism in thalassemia and sickle cell disease 138
Erythrocytapheresis plus erythropoietin: An alternative therapy for selected patients with hemochromatosis and severe organ damage 132
MR imaging of cerebral cortical involvement in aceruloplasminemia 128
Reduced insulin sensitivity is associated with adrenergic overdrive in hemochromatosis independently on obesity and hypertension 128
Identification of novel mutations by targeted NGS panel in patients with hyperferritinemia 127
Interaction Between the PNPLA3 I148M Mutation, Body Weight, And Steatosis, In Determining The Progression To Cirrhosis In Hereditary Hemochromatosis 126
Hepcidin modulation in human diseases: From research to clinic 116
GH deficiency in adult B-thalassemia major patients and its relationship with IGF-1 production 108
Interaction between the PNPLA3 I148M mutation and body weight in determining steatosis and the progression to cirrhosis in hereditary hemochromatosis 101
Hereditary Hyperferritinemia 57
Haemochromatosis in children: A national retrospective cohort promoted by the A.I.E.O.P. (Associazione Italiana Emato-Oncologia Pediatrica) study group 52
Reference Values of Ceruloplasmin across the Adult Age Range in a Large Italian Healthy Population 42
Totale 10.068
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Categoria #
all - tutte 34.159
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 34.159
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020147 0 0 0 0 0 0 0 0 0 0 121 26
2020/20211.072 62 53 112 117 99 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
2023/2024886 38 42 42 32 95 252 173 59 36 9 10 98
2024/20251.518 94 201 108 84 206 71 104 125 204 318 3 0
Totale 10.068