IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

MUZZA, MARINA
 Distribuzione geografica
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Continente #
EU - Europa 3.676
AS - Asia 3.211
NA - Nord America 3.134
SA - Sud America 254
AF - Africa 65
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 1
Totale 10.347
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Nazione #
US - Stati Uniti d'America 3.003
GB - Regno Unito 1.143
SG - Singapore 1.025
CN - Cina 989
IT - Italia 740
DE - Germania 441
SE - Svezia 323
VN - Vietnam 289
HK - Hong Kong 285
RU - Federazione Russa 278
NL - Olanda 179
BR - Brasile 159
BD - Bangladesh 156
IN - India 143
FR - Francia 133
UA - Ucraina 130
CA - Canada 96
TR - Turchia 84
KR - Corea 79
IE - Irlanda 76
FI - Finlandia 71
EU - Europa 47
CO - Colombia 38
CI - Costa d'Avorio 34
DK - Danimarca 33
JP - Giappone 32
ID - Indonesia 31
AR - Argentina 28
BE - Belgio 23
PL - Polonia 22
ES - Italia 18
UZ - Uzbekistan 15
IQ - Iraq 14
MX - Messico 12
GR - Grecia 11
ZA - Sudafrica 11
EC - Ecuador 8
PH - Filippine 8
VE - Venezuela 8
JO - Giordania 7
RO - Romania 7
SK - Slovacchia (Repubblica Slovacca) 7
AT - Austria 6
CH - Svizzera 6
CL - Cile 6
IR - Iran 6
AE - Emirati Arabi Uniti 5
EG - Egitto 5
HR - Croazia 5
TH - Thailandia 5
CR - Costa Rica 4
IL - Israele 4
JM - Giamaica 4
KZ - Kazakistan 4
LV - Lettonia 4
NP - Nepal 4
PK - Pakistan 4
PT - Portogallo 4
AU - Australia 3
BO - Bolivia 3
KE - Kenya 3
LT - Lituania 3
MA - Marocco 3
PY - Paraguay 3
TW - Taiwan 3
BH - Bahrain 2
BN - Brunei Darussalam 2
DO - Repubblica Dominicana 2
ET - Etiopia 2
GT - Guatemala 2
HN - Honduras 2
KG - Kirghizistan 2
LB - Libano 2
MD - Moldavia 2
MT - Malta 2
NZ - Nuova Zelanda 2
OM - Oman 2
PA - Panama 2
PR - Porto Rico 2
SA - Arabia Saudita 2
TT - Trinidad e Tobago 2
AL - Albania 1
AM - Armenia 1
AO - Angola 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BS - Bahamas 1
CZ - Repubblica Ceca 1
DZ - Algeria 1
GH - Ghana 1
GL - Groenlandia 1
HU - Ungheria 1
IS - Islanda 1
KW - Kuwait 1
LU - Lussemburgo 1
MY - Malesia 1
NO - Norvegia 1
NR - Nauru 1
PE - Perù 1
PS - Palestinian Territory 1
Totale 10.384
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Città #
Southend 1.074
Singapore 640
Ashburn 363
Chandler 307
Hong Kong 261
Milan 228
San Jose 223
Beijing 216
Frankfurt am Main 152
Seattle 118
Council Bluffs 112
Princeton 108
Dallas 101
Ho Chi Minh City 93
Ann Arbor 91
Jacksonville 91
New York 88
Wilmington 86
Los Angeles 85
Dublin 75
Hanoi 73
Bengaluru 70
Santa Clara 66
Toronto 60
Somerville 58
Nanjing 55
Redmond 49
Lauterbourg 47
Hefei 43
Buffalo 41
Dearborn 41
Des Moines 41
Shanghai 40
Kent 39
Boardman 37
Rome 35
Woodbridge 35
Abidjan 34
Bogotá 33
Fairfield 33
Mountain View 33
Sakarya 32
Moscow 31
Serra 31
Andover 30
Changsha 30
The Dalles 30
Bühl 29
Guangzhou 28
Helsinki 28
Columbus 27
Jinan 27
Tokyo 27
Bologna 24
Houston 23
Nanchang 23
São Paulo 23
Hebei 22
Jakarta 22
Ottawa 20
Redwood City 20
Shenyang 20
Cangzhou 19
Brussels 18
Haiphong 15
Warsaw 15
Zhengzhou 15
Berlin 14
Da Nang 14
Eitensheim 14
Hangzhou 14
Chicago 13
San Diego 13
Tianjin 13
Athens 12
Düsseldorf 12
Naples 12
Phoenix 12
Turin 12
Fuzhou 11
Seoul 11
Florence 10
Munich 10
Nuremberg 10
Cambridge 9
Istanbul 9
Lecco 9
Tashkent 9
Kunming 8
London 8
Ningbo 8
Taizhou 8
Verona 8
Bernolákovo 7
Besnate 7
Biên Hòa 7
Brescia 7
Falls Church 7
Haikou 7
Hanover 7
Totale 6.436
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Nome #
Impact of Mutation Density and Heterogeneity on Papillary Thyroid Cancer Clinical Features and Remission Probability 664
The thyroid risk score (TRS) for nodules with indeterminate cytology 279
Microchimerismo cellulare fetale nel carcinoma papillare della tiroide 267
High phenotypic intrafamilial variability in patients with Pendred syndrome and a novel duplication in the SLC26A4 gene: clinical characterization and functional studies of the mutated SLC26A4 protein 263
Fetal cell microchimerism in papillary thyroid cancer : a possibile role in tumor demage and tissue repair 254
Retinal photoreceptor functions are compromised in patients with resistance to thyroid hormone syndrome (RTHβ) 250
Absence of BRAF mutations in endocrine tumors 247
Telomerase in differentiated thyroid cancer : promoter mutations, expression and localization 241
Thyroid cancer harboring PTEN and TP53 mutations: A peculiar molecular and clinical case report 234
Allelic distribution of six RET polymorphisms in sporadic medullary thyroid cancer and functional analysis of G691S variant 227
Fetal cell microchimerism in papillary thyroid cancer 225
An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyrod carcinoma 224
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism 222
MassARRAY-based simultaneous detection of hotspot somatic mutations and recurrent fusion genes in papillary thyroid carcinoma : the PTC-MA assay 217
Fetal cell microchimerism in papillary thyroid cancer : a role in the outcome of the disease 215
The tight relationship between papillary thyroid cancer, autoimmunity and inflammation : clinical and molecular studies 214
Fetal cell microchimerism in papillary thyroid cancer : studies in peripheral blood and tissues 212
Analisi funzionale di una complessa mutazione germinale localizzata nel dominio iuxtamembrana del gene RET in un carcinoma midollare familiare 211
Papillary thyroid carcinoma and infammation 211
Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing loss 210
Combined Mutational and Clonality Analyses Support the Existence of Intra-Tumor Heterogeneity in Papillary Thyroid Cancer 209
BRAF mutations in an Italian series of thyroid cancers 208
Gitelman’s sindrome : description of a new case in a family with RTH 207
Fetal cell microchimerism in papillary thyroid cancer : a possible role in tumour demage and tissue repair 207
Absence of sonic hedgehog mutations in a large cohort of children with thyroid dysgenesis 202
RET genotypes comprising specific haplotypes of polymorphic variants are associated with sporadic medullary thyroid cancer 201
An in-frame complex mutation in the juxtamembarne intracellular domain causing RET activation in a familial medullary thyroid carcinoma 195
RET genotypes in sporadic medullary thyroid cancer : studies in a large Italian series 190
FAM83B is involved in thyroid cancer cell differentiation and migration 187
Gonadal structures in a fetus with complete androgen insensitivity syndrome and persistent Müllerian derivatives : comparison with normal fetal development 187
The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects 184
Analysis of a deiodinase 2 polymorphism (oRFa-Asp) in patients with Graves’ disease and controls : preliminary results 183
Oxidative Stress Correlates with More Aggressive Features in Thyroid Cancer 180
Molecular analysis in three cases of medullary and papillary thyroid carcinoma occurring as collision tumors 175
Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism 173
The role of Ret genotypes as modifier loci for sporadic medullary cancer 172
Genetics and management of congenital hypothyroidism 171
Histopathological and molecular studies in patients with goiter and hypercalcitoninemia : reactive or neoplastic C-cell hyperplasia? 167
Absence of sonic hedgehog (Shh) germline mutations in patients with thyroid dysgenesis 157
Fetal microchimerism in women with thyroid cancer 148
Fetal cell microchimerism in women with thyroid cancer 146
Letter regarding the article: "Multiple HABP2 variants in familial papillary thyroid carcinoma: Contribution of a group of "thyroid-checked" controls" by Kern et al 146
BRAF mutations in an Italian cohort of thyroid cancers 144
The BRAF-inhibitor PLX4720 inhibits CXCL8 secretion in BRAFV600E mutated and normal thyroid cells : a further anti-cancer effect of BRAF-inhibitors 143
DUOX2/DUOXA2 Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom 143
Pendred’s sindrome : from genotype to phenotype 141
Fetal cell microchimerism in papillary thyroid cancer 141
Segregation and expression analyses of hyaluronan-binding protein 2 (HABP2) : insights from a large series of familial non-medullary thyroid cancers and literature review 139
Disorders of H2O2 generation 138
DUOXS defects : genotype-phenotype correlations 128
New genetics in congenital hypothyroidism 121
RET gene screening in patients with sporadic medullary thyroid carcinoma and functional characterization of a novel RET mutation 120
Oxidative stress and the subcellular localization of the telomerase reverse transcriptase (TERT) in papillary thyroid cancer 119
Four novel RET germline variants in exons 8 and 11 display an oncogenic potential in vitro 95
An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyroid carcinoma 93
Clinical relevance of the thyroid differentiation score (TDS) in benign and malignant thyroid tumors 82
Totale 10.829
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Categoria #
all - tutte 29.198
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 29.198
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021179 0 0 0 0 0 0 0 0 0 0 113 66
2021/2022692 88 55 31 38 47 27 58 28 86 53 45 136
2022/2023945 118 106 99 101 111 166 21 63 86 8 46 20
2023/2024758 19 57 17 60 210 62 47 42 41 58 62 83
2024/20251.447 67 136 43 151 101 74 48 153 75 177 136 286
2025/20263.328 348 200 284 250 395 230 544 143 293 267 374 0
Totale 10.829