Bicocca Open Archive

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MARIANI, RAFFAELLA
 Distribuzione geografica
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Continente #
NA - Nord America 9.224
AS - Asia 3.611
EU - Europa 3.351
SA - Sud America 596
Continente sconosciuto - Info sul continente non disponibili 298
AF - Africa 78
OC - Oceania 9
Totale 17.167
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Nazione #
US - Stati Uniti d'America 8.746
SG - Singapore 1.333
CN - Cina 897
IT - Italia 547
DE - Germania 529
BR - Brasile 443
RU - Federazione Russa 437
HK - Hong Kong 433
SE - Svezia 432
CA - Canada 415
VN - Vietnam 363
IE - Irlanda 304
UA - Ucraina 255
GB - Regno Unito 241
FR - Francia 161
IN - India 125
FI - Finlandia 113
AT - Austria 92
KR - Corea 65
TR - Turchia 60
BD - Bangladesh 58
AR - Argentina 57
BE - Belgio 43
IQ - Iraq 41
NL - Olanda 41
DK - Danimarca 39
MX - Messico 38
JP - Giappone 35
PK - Pakistan 33
CO - Colombia 30
ES - Italia 28
ID - Indonesia 27
PH - Filippine 23
SA - Arabia Saudita 20
ZA - Sudafrica 20
PL - Polonia 19
UZ - Uzbekistan 18
VE - Venezuela 16
EC - Ecuador 15
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
CR - Costa Rica 4
DZ - Algeria 4
UY - Uruguay 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
AM - Armenia 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
TT - Trinidad e Tobago 2
AL - Albania 1
BB - Barbados 1
BH - Bahrain 1
BW - Botswana 1
BY - Bielorussia 1
BZ - Belize 1
CG - Congo 1
EE - Estonia 1
GH - Ghana 1
Totale 16.849
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Città #
Ann Arbor 1.283
Ashburn 900
Singapore 810
Woodbridge 582
San Jose 465
Fairfield 447
Houston 427
Hong Kong 420
Chandler 394
Dublin 297
Toronto 289
Frankfurt am Main 273
Jacksonville 270
Wilmington 263
New York 229
Dearborn 198
Seattle 172
Milan 167
Los Angeles 162
Cambridge 158
Beijing 151
Santa Clara 142
Council Bluffs 127
Princeton 115
Chicago 105
Ho Chi Minh City 102
Dallas 100
Nanjing 96
The Dalles 90
Hanoi 84
Vienna 81
Hefei 76
Boardman 63
Shanghai 63
Buffalo 59
Seoul 57
Rome 54
Lawrence 49
Lauterbourg 48
São Paulo 47
Lachine 45
Altamura 44
Munich 44
Orem 39
Brussels 38
Helsinki 38
Moscow 36
San Diego 36
Nanchang 29
Atlanta 28
Dong Ket 26
Phoenix 26
Denver 25
San Francisco 25
Turku 25
Ottawa 24
Tokyo 24
Changsha 23
London 23
Shenyang 23
Turin 23
Boston 21
Chennai 20
Brooklyn 19
Columbus 19
Hebei 19
Zhengzhou 19
Jinan 18
Montreal 18
Guangzhou 17
Philadelphia 17
Rio de Janeiro 17
Andover 16
Tampa 15
Da Nang 14
Jiaxing 14
Tashkent 14
Tianjin 14
Dhaka 13
Haiphong 13
Jakarta 13
Belo Horizonte 12
Brasília 12
Indianapolis 12
Mexico City 12
Ningbo 12
Washington 12
Baghdad 11
Huizen 11
Lahore 10
Stockholm 10
Warsaw 10
Auburn Hills 9
Campinas 9
Nuremberg 9
Paris 9
Charlotte 8
Fremont 8
Hangzhou 8
Istanbul 8
Totale 11.081
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Nome #
Reference Values of Ceruloplasmin across the Adult Age Range in a Large Italian Healthy Population 905
Hepcidin regulation in a mouse model of acute hypoxia 607
Phenotypic heterogeneity in seven Italian cases of aceruloplasminemia 456
GNPAT rs11558492 is not a major modifier of iron status: Study of Italian hemochromatosis patients and blood donors 421
Serum ferritin and liver features in a cohort of 15 patients affected by Gaucher disease 419
Re-evaluation of clinical and histological criteria for diagnosis of dysmetabolic iron overload syndrome 392
A severe hemojuvelin mutation leading to late onset of HFE2-hemochromatosis 392
Hif1a: A putative modifier of hemochromatosis 392
Prolonged exposure to welding fumes as a novel cause of systemic iron overload 363
Inherited iron overload disorders 358
Hepcidin regulation in a mouse model of acute hypoxia 355
Type 3 hemochromatosis and beta-thalassemia trait 350
Expression of hepcidin and other iron-related genes in type 3 hemochromatosis due to a novel mutation in transferrin receptor-2 347
Genetic and metabolic factors are associated with increased hepatic iron stores in a selected population of p.Cys282Tyr heterozygotes 344
Novel mutations of the ferroportin gene (SLC40A1): Analysis of 56 consecutive patients with unexplained iron overload 342
The presence of two or more metabolic alterations and hepatic steatosis characterizes the dysmetabolic iron overload syndrome 338
Transferrin receptor 2 mutations in patients with juvenile hemochromatosis phenotype 338
Alterations in sympathetic nerve traffic in genetic haemochromatosis before and after iron depletion therapy: A microneurographic study 336
Unexplained isolated hyperferritinemia without iron overload 334
CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients 320
Hepcidin and iron-related gene expression in subjects with Dysmetabolic Hepatic Iron Overload 309
Heterogeneity of iron overload: Clinical, biochemical, histopathologic and genetic study of 70 patients 305
Dysmetabolic Hepatic Iron Overload Syndrome: Analysis of Hepcidin Response to Acute Oral Iron and Chronic Iron Overload 305
Proprotein convertase 7 rs236918 associated with liver fibrosis in Italian patients with HFE-related hemochromatosis 303
Prevalence of HFE mutations in upper northern Italy: study of 1132 unrelated blood donors 300
Does aceruloplasminemia modulate iron phenotype in thalassemia intermedia? 297
UNEXPLAINED ISOLATED HYPERFERRITINEMIA IN PATIENTS WITHOUT MUTATIONS IN FERRITIN GENE AND L-FERRITIN IRES REGIONS 292
Iron Overload Increases Sympathetic Nervous Activity: Study in Hemochromatosis Patients at Diagnosis and Iron Depletion 288
Increased serum ferritin is common in men with essential hypertension 286
Hepcidin expression in iron overload diseases is variably modulated by circulating factors 286
Hereditary Hyperferritinemia 283
Il sovraccarico di ferro: modulatore della risposta adrenergica 277
HFE and SLC40A1 polymorphisms in patients with unexplained iron overload 276
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 274
Identification of novel mutations by targeted NGS panel in patients with hyperferritinemia 274
Prevalence of C282Y and E168X HFE mutations in an italian population of northern european ancestry 267
Effects of plasma transfusion on hepcidin production in human congenital hypotransferrinemia 265
Reduced expression of hepcidin in patients with myelodysplastic syndrome and myelofibrosis: The causes might be more heterogeneous than in thalassaemia 264
GNPAT rs11558492 is not associated to iron overload in Italian HFE p.C282Y homozygotes 261
Analysis of Polymorphisms of Genes Regulating Hepcidin Transcription in Hfe-Hemochromatosis 260
Haemochromatosis in patients with β-thalassaemia trait 241
Homozygous deletion of HFE: The Sardinian hemochromatosis? 241
Natural history of juvenile haemochromatosis 233
Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation 229
Reduced Insulin Sensitivity is Associated with Adrenergic Overdrive Independently on Obesity and Hypertension 226
Homozygosity for transferrin receptor-2 y250x mutation induces early iron overload 220
Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosis 220
Iron accumulation in chronic hepatitis C: relation of hepatic iron distribution, HFE genotype, and disease course 216
Hepcidin modulation in human diseases: From research to clinic 207
Iron metabolism in thalassemia and sickle cell disease 202
Erythrocytapheresis plus erythropoietin: An alternative therapy for selected patients with hemochromatosis and severe organ damage 201
Reduced insulin sensitivity is associated with adrenergic overdrive in hemochromatosis independently on obesity and hypertension 201
Interaction Between the PNPLA3 I148M Mutation, Body Weight, And Steatosis, In Determining The Progression To Cirrhosis In Hereditary Hemochromatosis 198
MR imaging of cerebral cortical involvement in aceruloplasminemia 194
GH deficiency in adult B-thalassemia major patients and its relationship with IGF-1 production 193
Interaction between the PNPLA3 I148M mutation and body weight in determining steatosis and the progression to cirrhosis in hereditary hemochromatosis 164
Totale 17.167
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Categoria #
all - tutte 52.004
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 52.004
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022721 0 0 101 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
2026/20271.258 614 451 193 0 0 0 0 0 0 0 0 0
Totale 17.167