UNICA IRIS Institutional Research Information System

SATTA, STEFANIA
 Distribuzione geografica
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Continente #
EU - Europa 47.774
NA - Nord America 3.561
AS - Asia 1.556
SA - Sud America 202
Continente sconosciuto - Info sul continente non disponibili 94
AF - Africa 51
OC - Oceania 7
Totale 53.245
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Nazione #
IT - Italia 46.572
US - Stati Uniti d'America 3.473
SG - Singapore 582
CN - Cina 566
UA - Ucraina 273
DE - Germania 267
SE - Svezia 258
VN - Vietnam 158
BR - Brasile 153
FI - Finlandia 104
GB - Regno Unito 81
FR - Francia 65
RU - Federazione Russa 57
CA - Canada 56
BD - Bangladesh 47
IN - India 35
HK - Hong Kong 26
KR - Corea 26
NL - Olanda 19
AR - Argentina 16
IQ - Iraq 15
BE - Belgio 14
IL - Israele 14
ES - Italia 13
JP - Giappone 12
TR - Turchia 12
AT - Austria 9
CL - Cile 9
MX - Messico 9
PL - Polonia 9
SC - Seychelles 9
EG - Egitto 7
JM - Giamaica 7
KE - Kenya 7
UZ - Uzbekistan 7
ZA - Sudafrica 7
CO - Colombia 6
ID - Indonesia 6
LT - Lituania 6
MA - Marocco 6
PE - Perù 6
AZ - Azerbaigian 5
CZ - Repubblica Ceca 5
TN - Tunisia 5
AE - Emirati Arabi Uniti 4
IR - Iran 4
JO - Giordania 4
MY - Malesia 4
NP - Nepal 4
NZ - Nuova Zelanda 4
PH - Filippine 4
PK - Pakistan 4
PS - Palestinian Territory 4
VE - Venezuela 4
BG - Bulgaria 3
DK - Danimarca 3
DZ - Algeria 3
EC - Ecuador 3
IE - Irlanda 3
LB - Libano 3
OM - Oman 3
PR - Porto Rico 3
PY - Paraguay 3
AU - Australia 2
BH - Bahrain 2
BZ - Belize 2
CG - Congo 2
CH - Svizzera 2
DO - Repubblica Dominicana 2
GP - Guadalupe 2
GR - Grecia 2
GT - Guatemala 2
HR - Croazia 2
SA - Arabia Saudita 2
SN - Senegal 2
AL - Albania 1
AM - Armenia 1
AO - Angola 1
BO - Bolivia 1
BY - Bielorussia 1
CW - ???statistics.table.value.countryCode.CW??? 1
CY - Cipro 1
ET - Etiopia 1
EU - Europa 1
GE - Georgia 1
GY - Guiana 1
HN - Honduras 1
HT - Haiti 1
HU - Ungheria 1
IM - Isola di Man 1
LV - Lettonia 1
MU - Mauritius 1
NR - Nauru 1
PT - Portogallo 1
RO - Romania 1
SV - El Salvador 1
TT - Trinidad e Tobago 1
VG - Isole Vergini Britanniche 1
Totale 53.153
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Città #
Cagliari 45.957
Ashburn 486
Uta 417
Singapore 334
Chandler 312
San Jose 243
Ann Arbor 199
Fairfield 170
Woodbridge 167
Nyköping 159
Jacksonville 138
Beijing 121
Dearborn 117
Houston 116
Boardman 115
Dallas 115
Wilmington 89
Seattle 80
Cambridge 63
Helsinki 61
Santa Clara 56
Shanghai 54
Ho Chi Minh City 50
Los Angeles 49
Council Bluffs 46
Nanjing 42
Lauterbourg 36
Hefei 35
Hanoi 34
Boston 33
The Dalles 28
Toronto 28
New York 27
Guangzhou 26
Seoul 26
Frankfurt am Main 24
São Paulo 23
Buffalo 21
Hong Kong 21
Munich 18
Milan 15
Redondo Beach 15
Brussels 13
Chicago 13
Da Nang 13
Jiaxing 13
San Diego 13
Denver 12
Princeton 12
Shenyang 12
Hebei 11
Nanchang 11
Tokyo 11
Amsterdam 10
Columbus 10
Montreal 10
Tianjin 10
Zhengzhou 10
Atlanta 9
London 9
Phoenix 9
Brooklyn 8
Dong Ket 8
Ottawa 8
Redwood City 8
Chennai 7
Kunming 7
Miami 7
Mountain View 7
Newark 7
Warsaw 7
Belo Horizonte 6
Changsha 6
New Delhi 6
Orem 6
Santiago 6
Stockholm 6
Tashkent 6
Washington 6
Augusta 5
Dhaka 5
Jinan 5
Johannesburg 5
Kingston 5
Manchester 5
Nairobi 5
Naples 5
Norwalk 5
Nuremberg 5
Philadelphia 5
Poplar 5
Rome 5
San Francisco 5
Turku 5
Vienna 5
Baku 4
Detroit 4
Erbil 4
Las Vegas 4
Mexico City 4
Totale 50.599
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Nome #
A genetic score for the prediction of beta-thalassemia severity 2.951
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia 2.350
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin 2.324
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation 2.307
IFNL3 polymorphisms and HCV infection in patients with beta thalassemia 2.197
HPFH from Klf1 haploinsufficiency combined to transcriptional heterozygous b-thalassemia 2.124
A validated cellular biobank for β-thalassemia 2.098
KLF1 gene mutations cause borderline HbA(2). 2.049
The problem of borderline hemoglobin A2 levels in the Screening for β-thalassemia carriers in Sardinia. 2.045
HPFH From Klf1 Haploinsufficiency Combined to Transcriptional Heterozygous β-Thalassemia 1.771
Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion 1.655
Delezione di regioni regolatorie dei geni alfa globinici, responsabili di una grave forma di emoglobina H 1.459
G-WAS in pazienti sardi con talassemia major e intermedia 1.457
Application of next generation sequencing to identify causative variants at the BCL11A locus 1.416
GENOME-WIDE ASSOCIATION STUDY FOR HB F DETERMINANTS IN SARDINIAN PATIENTS WITH Β THALASSEMIA 1.386
. “Variazioni al locus IL28B in pazienti sardi con talassemia major HCV positivi” 1.296
“Hb Sassari [α126 (H9) ASP→HIS] result from a GAC→CAC mutation in the α1-globin gene” 1.265
Polymorphism of S-transferase glutathione gene and a major thalassaemia cardiac iron 1.213
Posttranslational deamidation of proteins: the case of hemoglobin J Sardegna [a50 (CD8) HIS→ASN→ASP] 1.195
Delayed fetal hemoglobin switching in subjects with KLF1 gene mutation. 1.167
I difetti emoglobinici e la loro valutazione di laboratorio 1.158
“Diagnosi di α e β talassemia” 1.123
Glutathione S-transferase se gene polymorphism and heart iron overload in Thalassemia major 1.078
Analysis of candidate SNPs for high Hb F in beta thalassemia intermedia patients 1.066
Red cell pyruvate kinase deficiency in Southern Sardinia. 1.065
“Genetic modifiers of fetal hemoglobin expression” 1.054
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach 1.054
Hb Belfast [β15(A12)Trp→Arg]: Definition of the clinical and hematological phenotype 976
Amelioration of Sardinian beta-zero thalassemia by genetic modifiers. 963
Alfa-thalassemia in Sardinia 940
Amelioration of Sardinian beta-zero thalassemia by genetic modifiers. 881
Hemoglobin Belfast (beta15, Trp→Arg) definition of the clinical and hematological phenotype 832
Chronic ethanol intoxication enhances [3H]CCPA binding and does not reduce A1 adenosine receptor function in rat cerebellum 647
“Chronic ethanol intoxication enhances [3H]CCPA binding and does not reduce A1 adenosine receptor function in rat cerebellum”. Pharmacology Biochemistry and Behavior vol.53, n°2, pp249-255, 1996 632
“Meccanismi molecolari delle sindromi talassemiche e induttori della sintesi di catene γ” Riv. Ital. Pediatr. Vol.24: 84-86, 1998 620
null 589
“Homozygosity for non deletion δβ° thalassemia resulting in a silent clinical phenotype” 504
Hemoglobin Belfast (beta15,Trp→Arg) definition of the clinical and hematological phenotype 486
5. Galanello R., Satta S., Pirroni M.G., Travi M. and Maccioni L. “Globin chain synthesis analysis by high performance liquid chromatography in the screening of thalassemia syndromes”. European Concerted Action-Evaluation of fetal Hemoglobin Activating Therapies. Hemoglobin vol.22 (5&6): 501-508, 1998 485
Studio del gene AHSP nelle β-Talassemie 464
“Neonatal Anemia” 453
Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major 205
Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case Series 123
Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major 122
Totale 53.245
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Categoria #
all - tutte 71.101
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 71.101
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.922 0 0 0 0 153 296 187 240 166 205 297 378
2022/20233.587 400 595 441 276 302 349 169 340 243 177 160 135
2023/20242.886 139 166 184 234 259 449 379 249 144 213 250 220
2024/20254.274 988 981 451 428 298 329 309 49 142 70 112 117
2025/20262.453 247 129 293 182 245 192 347 114 152 329 144 79
2026/2027659 26 56 230 282 65 0 0 0 0 0 0 0
Totale 53.245