UNICA IRIS Institutional Research Information System

SATTA, STEFANIA
 Distribuzione geografica
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Continente #
EU - Europa 47.622
NA - Nord America 2.922
AS - Asia 1.496
SA - Sud America 186
AF - Africa 41
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 1
Totale 52.275
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Nazione #
IT - Italia 46.476
US - Stati Uniti d'America 2.870
SG - Singapore 574
CN - Cina 561
UA - Ucraina 272
DE - Germania 267
SE - Svezia 248
VN - Vietnam 158
BR - Brasile 143
FI - Finlandia 104
GB - Regno Unito 74
FR - Francia 56
CA - Canada 35
RU - Federazione Russa 33
IN - India 32
KR - Corea 26
HK - Hong Kong 25
BD - Bangladesh 22
NL - Olanda 18
IQ - Iraq 15
AR - Argentina 14
BE - Belgio 14
ES - Italia 12
JP - Giappone 12
TR - Turchia 10
AT - Austria 9
MX - Messico 9
CL - Cile 8
PL - Polonia 8
KE - Kenya 7
UZ - Uzbekistan 7
ZA - Sudafrica 7
EG - Egitto 6
ID - Indonesia 6
LT - Lituania 6
MA - Marocco 6
AZ - Azerbaigian 5
CO - Colombia 5
TN - Tunisia 5
CZ - Repubblica Ceca 4
IR - Iran 4
JO - Giordania 4
MY - Malesia 4
NP - Nepal 4
NZ - Nuova Zelanda 4
PE - Perù 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
CG - Congo 2
CH - Svizzera 2
DK - Danimarca 2
DO - Repubblica Dominicana 2
GR - Grecia 2
HR - Croazia 2
JM - Giamaica 2
SN - Senegal 2
AL - Albania 1
AM - Armenia 1
AO - Angola 1
BO - Bolivia 1
BY - Bielorussia 1
BZ - Belize 1
CY - Cipro 1
ET - Etiopia 1
EU - Europa 1
GE - Georgia 1
GP - Guadalupe 1
GT - Guatemala 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
Totale 52.275
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Città #
Cagliari 45.900
Uta 417
Singapore 330
Chandler 312
Ashburn 272
Ann Arbor 199
San Jose 190
Fairfield 169
Woodbridge 167
Nyköping 159
Jacksonville 138
Beijing 118
Dearborn 117
Boardman 115
Houston 113
Dallas 111
Wilmington 89
Seattle 79
Cambridge 63
Helsinki 61
Shanghai 54
Ho Chi Minh City 50
Santa Clara 50
Los Angeles 47
Nanjing 42
Lauterbourg 36
Hefei 35
Hanoi 34
Boston 32
The Dalles 28
Guangzhou 26
Seoul 26
Frankfurt am Main 24
Hong Kong 20
Toronto 19
Buffalo 18
Munich 18
São Paulo 17
New York 16
Redondo Beach 15
Brussels 13
Da Nang 13
Jiaxing 13
Milan 12
San Diego 12
Shenyang 12
Hebei 11
Nanchang 11
Tokyo 11
Denver 10
Tianjin 10
Zhengzhou 10
Amsterdam 9
London 9
Chicago 8
Council Bluffs 8
Dong Ket 8
Redwood City 8
Brooklyn 7
Chennai 7
Kunming 7
Mountain View 7
Warsaw 7
Belo Horizonte 6
Changsha 6
Montreal 6
New Delhi 6
Orem 6
Stockholm 6
Tashkent 6
Atlanta 5
Augusta 5
Columbus 5
Dhaka 5
Jinan 5
Johannesburg 5
Manchester 5
Nairobi 5
Norwalk 5
Nuremberg 5
Ottawa 5
Poplar 5
San Francisco 5
Santiago 5
Turku 5
Vienna 5
Baku 4
Detroit 4
Erbil 4
Mexico City 4
Naples 4
Ningbo 4
Orange 4
Phoenix 4
Pune 4
Rio de Janeiro 4
Taizhou 4
Tây Ninh 4
Verona 4
Amman 3
Totale 50.126
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Nome #
A genetic score for the prediction of beta-thalassemia severity 2.913
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia 2.337
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin 2.306
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation 2.275
IFNL3 polymorphisms and HCV infection in patients with beta thalassemia 2.173
A validated cellular biobank for β-thalassemia 2.075
HPFH from Klf1 haploinsufficiency combined to transcriptional heterozygous b-thalassemia 2.071
KLF1 gene mutations cause borderline HbA(2). 2.039
The problem of borderline hemoglobin A2 levels in the Screening for β-thalassemia carriers in Sardinia. 2.029
HPFH From Klf1 Haploinsufficiency Combined to Transcriptional Heterozygous β-Thalassemia 1.728
Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion 1.635
G-WAS in pazienti sardi con talassemia major e intermedia 1.445
Delezione di regioni regolatorie dei geni alfa globinici, responsabili di una grave forma di emoglobina H 1.445
Application of next generation sequencing to identify causative variants at the BCL11A locus 1.400
GENOME-WIDE ASSOCIATION STUDY FOR HB F DETERMINANTS IN SARDINIAN PATIENTS WITH Β THALASSEMIA 1.370
. “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” 1.255
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 1.156
Delayed fetal hemoglobin switching in subjects with KLF1 gene mutation. 1.148
I difetti emoglobinici e la loro valutazione di laboratorio 1.145
“Diagnosi di α e β talassemia” 1.074
Glutathione S-transferase se gene polymorphism and heart iron overload in Thalassemia major 1.060
Red cell pyruvate kinase deficiency in Southern Sardinia. 1.051
Analysis of candidate SNPs for high Hb F in beta thalassemia intermedia patients 1.048
“Genetic modifiers of fetal hemoglobin expression” 1.041
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach 1.030
Hb Belfast [β15(A12)Trp→Arg]: Definition of the clinical and hematological phenotype 952
Amelioration of Sardinian beta-zero thalassemia by genetic modifiers. 950
Alfa-thalassemia in Sardinia 916
Amelioration of Sardinian beta-zero thalassemia by genetic modifiers. 868
Hemoglobin Belfast (beta15, Trp→Arg) definition of the clinical and hematological phenotype 822
Chronic ethanol intoxication enhances [3H]CCPA binding and does not reduce A1 adenosine receptor function in rat cerebellum 633
“Meccanismi molecolari delle sindromi talassemiche e induttori della sintesi di catene γ” Riv. Ital. Pediatr. Vol.24: 84-86, 1998 606
null 589
“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 586
“Homozygosity for non deletion δβ° thalassemia resulting in a silent clinical phenotype” 496
Hemoglobin Belfast (beta15,Trp→Arg) definition of the clinical and hematological phenotype 476
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 470
“Neonatal Anemia” 448
Studio del gene AHSP nelle β-Talassemie 438
Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major 184
Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major 110
Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case Series 95
Totale 52.366
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Categoria #
all - tutte 67.417
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 67.417
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021916 0 0 0 0 0 0 0 0 0 0 478 438
2021/20222.745 242 157 208 216 153 296 187 240 166 205 297 378
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
2025/20262.233 247 129 293 182 245 192 347 114 152 329 3 0
Totale 52.366