UNICA IRIS Institutional Research Information System

SATTA, STEFANIA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 47.688
NA - Nord America 3.105
AS - Asia 1.531
SA - Sud America 191
Continente sconosciuto - Info sul continente non disponibili 92
AF - Africa 42
OC - Oceania 7
Totale 52.656
Salva come PNG Salva come JPEG
Nazione #
IT - Italia 46.534
US - Stati Uniti d'America 3.041
SG - Singapore 581
CN - Cina 564
UA - Ucraina 272
DE - Germania 267
SE - Svezia 249
VN - Vietnam 158
BR - Brasile 146
FI - Finlandia 104
GB - Regno Unito 74
FR - Francia 61
BD - Bangladesh 46
CA - Canada 41
RU - Federazione Russa 33
IN - India 32
HK - Hong Kong 26
KR - Corea 26
NL - Olanda 18
IQ - Iraq 15
AR - Argentina 14
BE - Belgio 14
ES - Italia 13
JP - Giappone 12
TR - Turchia 10
AT - Austria 9
MX - Messico 9
CL - Cile 8
PL - Polonia 8
EG - Egitto 7
KE - Kenya 7
UZ - Uzbekistan 7
ZA - Sudafrica 7
ID - Indonesia 6
LT - Lituania 6
MA - Marocco 6
PE - Perù 6
AZ - Azerbaigian 5
CO - Colombia 5
CZ - Repubblica Ceca 5
JM - Giamaica 5
TN - Tunisia 5
IR - Iran 4
JO - Giordania 4
MY - Malesia 4
NP - Nepal 4
NZ - Nuova Zelanda 4
PH - Filippine 4
PS - Palestinian Territory 4
VE - Venezuela 4
AE - Emirati Arabi Uniti 3
BG - Bulgaria 3
DZ - Algeria 3
EC - Ecuador 3
IE - Irlanda 3
LB - Libano 3
OM - Oman 3
PK - Pakistan 3
PY - Paraguay 3
AU - Australia 2
BH - Bahrain 2
BZ - Belize 2
CG - Congo 2
CH - Svizzera 2
DK - Danimarca 2
DO - Repubblica Dominicana 2
GR - Grecia 2
GT - Guatemala 2
HR - Croazia 2
SN - Senegal 2
AL - Albania 1
AM - Armenia 1
AO - Angola 1
BO - Bolivia 1
BY - Bielorussia 1
CY - Cipro 1
ET - Etiopia 1
EU - Europa 1
GE - Georgia 1
GP - Guadalupe 1
GY - Guiana 1
HU - Ungheria 1
IL - Israele 1
IM - Isola di Man 1
LV - Lettonia 1
MU - Mauritius 1
NR - Nauru 1
PR - Porto Rico 1
PT - Portogallo 1
RO - Romania 1
SA - Arabia Saudita 1
TT - Trinidad e Tobago 1
Totale 52.565
Salva come PNG Salva come JPEG
Città #
Cagliari 45.934
Uta 417
Singapore 334
Chandler 312
Ashburn 279
Ann Arbor 199
San Jose 198
Fairfield 169
Woodbridge 167
Nyköping 159
Jacksonville 138
Beijing 121
Dearborn 117
Boardman 115
Houston 115
Dallas 112
Wilmington 89
Seattle 79
Cambridge 63
Helsinki 61
Shanghai 54
Santa Clara 53
Ho Chi Minh City 50
Los Angeles 49
Nanjing 42
Council Bluffs 41
Lauterbourg 36
Hefei 35
Hanoi 34
Boston 32
The Dalles 28
Guangzhou 26
New York 26
Seoul 26
Frankfurt am Main 24
Hong Kong 21
Toronto 21
Buffalo 20
Munich 18
São Paulo 17
Redondo Beach 15
Milan 14
Brussels 13
Da Nang 13
Jiaxing 13
San Diego 12
Shenyang 12
Hebei 11
Nanchang 11
Tokyo 11
Denver 10
Tianjin 10
Zhengzhou 10
Amsterdam 9
Chicago 9
London 9
Columbus 8
Dong Ket 8
Redwood City 8
Brooklyn 7
Chennai 7
Kunming 7
Montreal 7
Mountain View 7
Ottawa 7
Phoenix 7
Warsaw 7
Belo Horizonte 6
Changsha 6
New Delhi 6
Orem 6
Stockholm 6
Tashkent 6
Atlanta 5
Augusta 5
Dhaka 5
Jinan 5
Johannesburg 5
Manchester 5
Nairobi 5
Norwalk 5
Nuremberg 5
Philadelphia 5
Poplar 5
San Francisco 5
Santiago 5
Turku 5
Vienna 5
Baku 4
Detroit 4
Erbil 4
Kingston 4
Mexico City 4
Miami 4
Naples 4
Ningbo 4
Orange 4
Pune 4
Rio de Janeiro 4
Rome 4
Totale 50.252
Salva come PNG Salva come JPEG
Nome #
A genetic score for the prediction of beta-thalassemia severity 2.928
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia 2.340
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin 2.310
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation 2.280
IFNL3 polymorphisms and HCV infection in patients with beta thalassemia 2.182
A validated cellular biobank for β-thalassemia 2.085
HPFH from Klf1 haploinsufficiency combined to transcriptional heterozygous b-thalassemia 2.075
KLF1 gene mutations cause borderline HbA(2). 2.044
The problem of borderline hemoglobin A2 levels in the Screening for β-thalassemia carriers in Sardinia. 2.034
HPFH From Klf1 Haploinsufficiency Combined to Transcriptional Heterozygous β-Thalassemia 1.754
Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion 1.644
Delezione di regioni regolatorie dei geni alfa globinici, responsabili di una grave forma di emoglobina H 1.451
G-WAS in pazienti sardi con talassemia major e intermedia 1.448
Application of next generation sequencing to identify causative variants at the BCL11A locus 1.406
GENOME-WIDE ASSOCIATION STUDY FOR HB F DETERMINANTS IN SARDINIAN PATIENTS WITH Β THALASSEMIA 1.374
. “Variazioni al locus IL28B in pazienti sardi con talassemia major HCV positivi” 1.290
“Hb Sassari [α126 (H9) ASP→HIS] result from a GAC→CAC mutation in the α1-globin gene” 1.260
Posttranslational deamidation of proteins: the case of hemoglobin J Sardegna [a50 (CD8) HIS→ASN→ASP] 1.188
Polymorphism of S-transferase glutathione gene and a major thalassaemia cardiac iron 1.163
I difetti emoglobinici e la loro valutazione di laboratorio 1.151
Delayed fetal hemoglobin switching in subjects with KLF1 gene mutation. 1.151
“Diagnosi di α e β talassemia” 1.076
Glutathione S-transferase se gene polymorphism and heart iron overload in Thalassemia major 1.064
Red cell pyruvate kinase deficiency in Southern Sardinia. 1.055
Analysis of candidate SNPs for high Hb F in beta thalassemia intermedia patients 1.053
“Genetic modifiers of fetal hemoglobin expression” 1.046
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach 1.038
Hb Belfast [β15(A12)Trp→Arg]: Definition of the clinical and hematological phenotype 959
Amelioration of Sardinian beta-zero thalassemia by genetic modifiers. 954
Alfa-thalassemia in Sardinia 918
Amelioration of Sardinian beta-zero thalassemia by genetic modifiers. 872
Hemoglobin Belfast (beta15, Trp→Arg) definition of the clinical and hematological phenotype 825
Chronic ethanol intoxication enhances [3H]CCPA binding and does not reduce A1 adenosine receptor function in rat cerebellum 646
“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 624
“Meccanismi molecolari delle sindromi talassemiche e induttori della sintesi di catene γ” Riv. Ital. Pediatr. Vol.24: 84-86, 1998 614
null 589
“Homozygosity for non deletion δβ° thalassemia resulting in a silent clinical phenotype” 500
Hemoglobin Belfast (beta15,Trp→Arg) definition of the clinical and hematological phenotype 480
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 473
“Neonatal Anemia” 448
Studio del gene AHSP nelle β-Talassemie 445
Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major 196
Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major 117
Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case Series 106
Totale 52.656
Salva come PNG Salva come JPEG
Categoria #
all - tutte 69.437
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 69.437
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.503 0 157 208 216 153 296 187 240 166 205 297 378
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
2026/202770 26 44 0 0 0 0 0 0 0 0 0 0
Totale 52.656