SATTA, STEFANIA
 Distribuzione geografica
Continente #
EU - Europa 47.347
NA - Nord America 2.617
AS - Asia 1.171
SA - Sud America 154
AF - Africa 22
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 1
Totale 51.319
Nazione #
IT - Italia 46.303
US - Stati Uniti d'America 2.574
CN - Cina 523
SG - Singapore 452
UA - Ucraina 270
DE - Germania 261
SE - Svezia 245
BR - Brasile 128
VN - Vietnam 75
FI - Finlandia 74
GB - Regno Unito 68
CA - Canada 32
RU - Federazione Russa 32
KR - Corea 26
IN - India 24
FR - Francia 16
BE - Belgio 13
NL - Olanda 13
JP - Giappone 10
AR - Argentina 9
BD - Bangladesh 9
ES - Italia 9
MX - Messico 9
IQ - Iraq 8
PL - Polonia 8
AT - Austria 7
TR - Turchia 7
LT - Lituania 6
HK - Hong Kong 5
UZ - Uzbekistan 5
ZA - Sudafrica 5
EG - Egitto 4
IR - Iran 4
NZ - Nuova Zelanda 4
BG - Bulgaria 3
CO - Colombia 3
CZ - Repubblica Ceca 3
EC - Ecuador 3
IE - Irlanda 3
JO - Giordania 3
MA - Marocco 3
PE - Perù 3
PS - Palestinian Territory 3
VE - Venezuela 3
AE - Emirati Arabi Uniti 2
AU - Australia 2
AZ - Azerbaigian 2
CG - Congo 2
CH - Svizzera 2
CL - Cile 2
DK - Danimarca 2
HR - Croazia 2
ID - Indonesia 2
KE - Kenya 2
MY - Malesia 2
NP - Nepal 2
PY - Paraguay 2
TN - Tunisia 2
AO - Angola 1
BO - Bolivia 1
BY - Bielorussia 1
BZ - Belize 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
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 51.319
Città #
Cagliari 45.734
Uta 417
Chandler 312
Ashburn 246
Singapore 225
Ann Arbor 199
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 46
Nanjing 42
Los Angeles 39
Hefei 35
Boston 32
Helsinki 31
Guangzhou 26
Ho Chi Minh City 26
Seoul 26
Toronto 19
Frankfurt am Main 18
Munich 18
Buffalo 17
São Paulo 16
Hanoi 15
Redondo Beach 15
New York 14
Jiaxing 13
The Dalles 13
Brussels 12
Milan 12
San Diego 12
Shenyang 12
Hebei 11
Nanchang 11
Denver 10
Tianjin 10
Tokyo 10
Zhengzhou 10
London 9
Da Nang 8
Dong Ket 8
Redwood City 8
Brooklyn 7
Council Bluffs 7
Mountain View 7
Warsaw 7
Amsterdam 6
Belo Horizonte 6
Changsha 6
Chicago 6
Kunming 6
Augusta 5
Chennai 5
Columbus 5
Jinan 5
Johannesburg 5
Montreal 5
New Delhi 5
Norwalk 5
Nuremberg 5
Poplar 5
Turku 5
Hong Kong 4
Mexico City 4
Naples 4
Ningbo 4
Orange 4
Ottawa 4
Phoenix 4
Pune 4
San Francisco 4
Stockholm 4
Taizhou 4
Tashkent 4
Verona 4
Vienna 4
Amman 3
Ankara 3
Atlanta 3
Auburn Hills 3
Biên Hòa 3
Dokki 3
Napoli 3
Rio de Janeiro 3
San Mateo 3
Sassari 3
Seville 3
Sofia 3
Turin 3
Auckland 2
Totale 49.431
Nome #
A genetic score for the prediction of beta-thalassemia severity 2.868
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia 2.281
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin 2.248
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation 2.243
IFNL3 polymorphisms and HCV infection in patients with beta thalassemia 2.150
A validated cellular biobank for β-thalassemia 2.032
HPFH from Klf1 haploinsufficiency combined to transcriptional heterozygous b-thalassemia 2.027
The problem of borderline hemoglobin A2 levels in the Screening for β-thalassemia carriers in Sardinia. 2.005
KLF1 gene mutations cause borderline HbA(2). 2.000
HPFH From Klf1 Haploinsufficiency Combined to Transcriptional Heterozygous β-Thalassemia 1.687
Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion 1.607
Delezione di regioni regolatorie dei geni alfa globinici, responsabili di una grave forma di emoglobina H 1.429
G-WAS in pazienti sardi con talassemia major e intermedia 1.427
Application of next generation sequencing to identify causative variants at the BCL11A locus 1.382
GENOME-WIDE ASSOCIATION STUDY FOR HB F DETERMINANTS IN SARDINIAN PATIENTS WITH Β THALASSEMIA 1.353
. “Variazioni al locus IL28B in pazienti sardi con talassemia major HCV positivi” 1.265
“Hb Sassari [α126 (H9) ASP→HIS] result from a GAC→CAC mutation in the α1-globin gene” 1.235
Posttranslational deamidation of proteins: the case of hemoglobin J Sardegna [a50 (CD8) HIS→ASN→ASP] 1.166
Polymorphism of S-transferase glutathione gene and a major thalassaemia cardiac iron 1.139
Delayed fetal hemoglobin switching in subjects with KLF1 gene mutation. 1.130
I difetti emoglobinici e la loro valutazione di laboratorio 1.124
“Diagnosi di α e β talassemia” 1.056
Glutathione S-transferase se gene polymorphism and heart iron overload in Thalassemia major 1.035
Red cell pyruvate kinase deficiency in Southern Sardinia. 1.033
Analysis of candidate SNPs for high Hb F in beta thalassemia intermedia patients 1.033
“Genetic modifiers of fetal hemoglobin expression” 1.024
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach 1.008
Hb Belfast [β15(A12)Trp→Arg]: Definition of the clinical and hematological phenotype 931
Amelioration of Sardinian beta-zero thalassemia by genetic modifiers. 930
Alfa-thalassemia in Sardinia 910
Amelioration of Sardinian beta-zero thalassemia by genetic modifiers. 856
Hemoglobin Belfast (beta15, Trp→Arg) definition of the clinical and hematological phenotype 812
Chronic ethanol intoxication enhances [3H]CCPA binding and does not reduce A1 adenosine receptor function in rat cerebellum 624
“Meccanismi molecolari delle sindromi talassemiche e induttori della sintesi di catene γ” Riv. Ital. Pediatr. Vol.24: 84-86, 1998 593
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 575
“Homozygosity for non deletion δβ° thalassemia resulting in a silent clinical phenotype” 487
Hemoglobin Belfast (beta15,Trp→Arg) definition of the clinical and hematological phenotype 466
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 460
“Neonatal Anemia” 436
Studio del gene AHSP nelle β-Talassemie 422
Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major 166
Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major 98
Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case Series 68
Totale 51.410
Categoria #
all - tutte 65.898
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 65.898


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
2025/20261.277 247 129 293 182 245 181 0 0 0 0 0 0
Totale 51.410