SATTA, STEFANIA
 Distribuzione geografica
Continente #
EU - Europa 47.328
NA - Nord America 2.605
AS - Asia 1.061
SA - Sud America 151
AF - Africa 18
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 1
Totale 51.171
Nazione #
IT - Italia 46.287
US - Stati Uniti d'America 2.563
CN - Cina 522
SG - Singapore 372
UA - Ucraina 270
DE - Germania 260
SE - Svezia 244
BR - Brasile 127
FI - Finlandia 74
GB - Regno Unito 68
VN - Vietnam 56
RU - Federazione Russa 32
CA - Canada 31
KR - Corea 26
IN - India 22
FR - Francia 16
BE - Belgio 13
NL - Olanda 13
AR - Argentina 9
BD - Bangladesh 9
ES - Italia 9
MX - Messico 9
JP - Giappone 8
PL - Polonia 8
AT - Austria 7
IQ - Iraq 7
LT - Lituania 6
TR - Turchia 6
EG - Egitto 4
HK - Hong Kong 4
IR - Iran 4
NZ - Nuova Zelanda 4
UZ - Uzbekistan 4
ZA - Sudafrica 4
BG - Bulgaria 3
CO - Colombia 3
CZ - Repubblica Ceca 3
PE - Perù 3
VE - Venezuela 3
AE - Emirati Arabi Uniti 2
AU - Australia 2
AZ - Azerbaigian 2
CH - Svizzera 2
CL - Cile 2
DK - Danimarca 2
EC - Ecuador 2
HR - Croazia 2
ID - Indonesia 2
IE - Irlanda 2
JO - Giordania 2
MA - Marocco 2
MY - Malesia 2
NP - Nepal 2
PS - Palestinian Territory 2
PY - Paraguay 2
TN - Tunisia 2
AO - Angola 1
BY - Bielorussia 1
BZ - Belize 1
CG - Congo 1
CY - Cipro 1
DZ - Algeria 1
EU - Europa 1
GE - Georgia 1
GP - Guadalupe 1
GR - Grecia 1
HU - Ungheria 1
IL - Israele 1
IM - Isola di Man 1
KE - Kenya 1
LB - Libano 1
LV - Lettonia 1
MU - Mauritius 1
NR - Nauru 1
OM - Oman 1
PH - Filippine 1
PT - Portogallo 1
RO - Romania 1
SA - Arabia Saudita 1
SN - Senegal 1
Totale 51.171
Città #
Cagliari 45.720
Uta 417
Chandler 312
Ashburn 244
Ann Arbor 199
Singapore 188
Fairfield 169
Woodbridge 167
Nyköping 159
Jacksonville 138
Dearborn 117
Boardman 115
Beijing 114
Houston 112
Dallas 109
Wilmington 89
Seattle 78
Cambridge 63
Shanghai 54
Santa Clara 45
Nanjing 42
Los Angeles 38
Hefei 35
Boston 32
Helsinki 31
Guangzhou 26
Seoul 26
Toronto 19
Munich 18
Buffalo 17
Frankfurt am Main 17
Ho Chi Minh City 17
Redondo Beach 15
São Paulo 15
Hanoi 13
Jiaxing 13
New York 13
Brussels 12
Milan 12
San Diego 12
Shenyang 12
Hebei 11
Nanchang 11
Denver 10
The Dalles 10
Tianjin 10
Zhengzhou 10
London 9
Dong Ket 8
Redwood City 8
Tokyo 8
Brooklyn 7
Mountain View 7
Warsaw 7
Amsterdam 6
Belo Horizonte 6
Changsha 6
Chicago 6
Kunming 6
Augusta 5
Columbus 5
Da Nang 5
Jinan 5
New Delhi 5
Norwalk 5
Nuremberg 5
Poplar 5
Turku 5
Chennai 4
Council Bluffs 4
Johannesburg 4
Mexico City 4
Montreal 4
Naples 4
Ningbo 4
Orange 4
Ottawa 4
Phoenix 4
Pune 4
San Francisco 4
Taizhou 4
Verona 4
Vienna 4
Atlanta 3
Auburn Hills 3
Biên Hòa 3
Dokki 3
Hong Kong 3
Napoli 3
Rio de Janeiro 3
San Mateo 3
Sassari 3
Seville 3
Sofia 3
Stockholm 3
Tashkent 3
Turin 3
Amman 2
Ankara 2
Auckland 2
Totale 49.343
Nome #
A genetic score for the prediction of beta-thalassemia severity 2.863
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia 2.276
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin 2.243
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation 2.237
IFNL3 polymorphisms and HCV infection in patients with beta thalassemia 2.147
A validated cellular biobank for β-thalassemia 2.025
HPFH from Klf1 haploinsufficiency combined to transcriptional heterozygous b-thalassemia 2.021
The problem of borderline hemoglobin A2 levels in the Screening for β-thalassemia carriers in Sardinia. 2.001
KLF1 gene mutations cause borderline HbA(2). 1.994
HPFH From Klf1 Haploinsufficiency Combined to Transcriptional Heterozygous β-Thalassemia 1.683
Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion 1.603
G-WAS in pazienti sardi con talassemia major e intermedia 1.425
Delezione di regioni regolatorie dei geni alfa globinici, responsabili di una grave forma di emoglobina H 1.424
Application of next generation sequencing to identify causative variants at the BCL11A locus 1.378
GENOME-WIDE ASSOCIATION STUDY FOR HB F DETERMINANTS IN SARDINIAN PATIENTS WITH Β THALASSEMIA 1.349
. “Variazioni al locus IL28B in pazienti sardi con talassemia major HCV positivi” 1.261
“Hb Sassari [α126 (H9) ASP→HIS] result from a GAC→CAC mutation in the α1-globin gene” 1.232
Posttranslational deamidation of proteins: the case of hemoglobin J Sardegna [a50 (CD8) HIS→ASN→ASP] 1.164
Polymorphism of S-transferase glutathione gene and a major thalassaemia cardiac iron 1.135
Delayed fetal hemoglobin switching in subjects with KLF1 gene mutation. 1.127
I difetti emoglobinici e la loro valutazione di laboratorio 1.122
“Diagnosi di α e β talassemia” 1.054
Glutathione S-transferase se gene polymorphism and heart iron overload in Thalassemia major 1.032
Red cell pyruvate kinase deficiency in Southern Sardinia. 1.031
Analysis of candidate SNPs for high Hb F in beta thalassemia intermedia patients 1.030
“Genetic modifiers of fetal hemoglobin expression” 1.021
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach 1.005
Amelioration of Sardinian beta-zero thalassemia by genetic modifiers. 927
Hb Belfast [β15(A12)Trp→Arg]: Definition of the clinical and hematological phenotype 927
Alfa-thalassemia in Sardinia 908
Amelioration of Sardinian beta-zero thalassemia by genetic modifiers. 852
Hemoglobin Belfast (beta15, Trp→Arg) definition of the clinical and hematological phenotype 809
Chronic ethanol intoxication enhances [3H]CCPA binding and does not reduce A1 adenosine receptor function in rat cerebellum 623
“Meccanismi molecolari delle sindromi talassemiche e induttori della sintesi di catene γ” Riv. Ital. Pediatr. Vol.24: 84-86, 1998 591
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 574
“Homozygosity for non deletion δβ° thalassemia resulting in a silent clinical phenotype” 485
Hemoglobin Belfast (beta15,Trp→Arg) definition of the clinical and hematological phenotype 463
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 458
“Neonatal Anemia” 434
Studio del gene AHSP nelle β-Talassemie 417
Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major 164
Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major 95
Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case Series 63
Totale 51.262
Categoria #
all - tutte 65.566
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 65.566


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20213.788 0 0 0 0 0 1.012 759 558 210 333 478 438
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
2025/20261.129 247 129 293 182 245 33 0 0 0 0 0 0
Totale 51.262