SAETTINI, FRANCESCO
 Distribuzione geografica
Continente #
NA - Nord America 3.594
AS - Asia 2.309
EU - Europa 1.704
SA - Sud America 330
Continente sconosciuto - Info sul continente non disponibili 258
AF - Africa 54
OC - Oceania 3
Totale 8.252
Nazione #
US - Stati Uniti d'America 3.362
SG - Singapore 748
IT - Italia 606
VN - Vietnam 498
CN - Cina 370
HK - Hong Kong 318
RU - Federazione Russa 255
BR - Brasile 242
CA - Canada 177
DE - Germania 160
SE - Svezia 142
IE - Irlanda 128
GB - Regno Unito 112
IN - India 79
FR - Francia 71
BD - Bangladesh 58
FI - Finlandia 52
TR - Turchia 34
AR - Argentina 33
NL - Olanda 30
UA - Ucraina 30
PL - Polonia 28
ID - Indonesia 25
JP - Giappone 24
KR - Corea 23
MX - Messico 23
ES - Italia 22
IQ - Iraq 21
PH - Filippine 18
PK - Pakistan 18
ZA - Sudafrica 17
DK - Danimarca 16
AT - Austria 15
CO - Colombia 15
SA - Arabia Saudita 11
VE - Venezuela 11
AE - Emirati Arabi Uniti 10
IL - Israele 10
CR - Costa Rica 9
EC - Ecuador 7
EG - Egitto 7
HN - Honduras 7
MY - Malesia 7
TN - Tunisia 7
CH - Svizzera 6
KE - Kenya 6
LT - Lituania 6
MA - Marocco 6
UZ - Uzbekistan 6
CL - Cile 5
PE - Perù 5
UY - Uruguay 5
AZ - Azerbaigian 4
BZ - Belize 4
ET - Etiopia 4
JO - Giordania 4
KZ - Kazakistan 4
PT - Portogallo 4
PY - Paraguay 4
BH - Bahrain 3
NI - Nicaragua 3
NP - Nepal 3
PA - Panama 3
PS - Palestinian Territory 3
SI - Slovenia 3
AL - Albania 2
BE - Belgio 2
BG - Bulgaria 2
BO - Bolivia 2
CZ - Repubblica Ceca 2
DO - Repubblica Dominicana 2
GR - Grecia 2
JM - Giamaica 2
LB - Libano 2
NZ - Nuova Zelanda 2
RO - Romania 2
TW - Taiwan 2
AM - Armenia 1
AO - Angola 1
AU - Australia 1
BW - Botswana 1
BY - Bielorussia 1
CY - Cipro 1
DZ - Algeria 1
EE - Estonia 1
GA - Gabon 1
GE - Georgia 1
GH - Ghana 1
GT - Guatemala 1
GY - Guiana 1
HU - Ungheria 1
KG - Kirghizistan 1
KW - Kuwait 1
LV - Lettonia 1
LY - Libia 1
MT - Malta 1
NG - Nigeria 1
NO - Norvegia 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
Totale 7.994
Città #
Ann Arbor 597
Singapore 448
Ashburn 366
Hong Kong 307
San Jose 264
Milan 194
Chandler 161
Ho Chi Minh City 158
Fairfield 154
Hanoi 129
Dublin 127
Toronto 125
Wilmington 111
Los Angeles 104
New York 102
Frankfurt am Main 101
Houston 83
Dallas 76
Santa Clara 68
Beijing 64
Seattle 55
The Dalles 52
Hefei 51
Woodbridge 51
Chicago 48
Buffalo 42
Princeton 38
Cambridge 37
Helsinki 34
Rome 32
São Paulo 32
Shanghai 31
Lauterbourg 29
Moscow 27
Da Nang 25
Boardman 23
Munich 23
Seoul 22
Dearborn 21
Montreal 21
Warsaw 21
Tokyo 20
Altamura 19
Council Bluffs 19
London 19
Chennai 18
Lawrence 18
Manchester 18
Monza 18
Brooklyn 17
Denver 17
Orem 17
Jacksonville 16
Jakarta 16
Phoenix 16
Atlanta 14
Boston 14
Haiphong 14
San Diego 12
Nanjing 11
Turku 11
Washington 11
Biên Hòa 10
Can Tho 10
City of London 10
Ha Long 10
Hải Dương 10
Stockholm 10
Turin 10
Casalecchio di Reno 9
Como 9
Johannesburg 9
Baghdad 8
Florence 8
Guangzhou 8
Ottawa 8
Seregno 8
Vienna 8
Ankara 7
Bologna 7
Changsha 7
Figino 7
Lissone 7
Medellín 7
Nuremberg 7
Poplar 7
Pune 7
Quận Một 7
Rio de Janeiro 7
San Francisco 7
San José 7
Belo Horizonte 6
Columbus 6
Curitiba 6
Guarulhos 6
Istanbul 6
Karachi 6
Kuala Lumpur 6
Paris 6
Tashkent 6
Totale 5.079
Nome #
Cardiofaciocutaneous syndrome and immunodeficiency: data from an international multicenter cohort 456
Biallelic PI4KA Mutations Disrupt B-Cell Metabolism and Cause B-Cell Lymphopenia and Hypogammaglobulinemia 408
Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency 391
A novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency 372
Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients 349
Two siblings presenting with novel ADA2 variants, lymphoproliferation, persistence of large granular lymphocytes, and T-cell perturbations 337
Intermittent granulocyte maturation arrest, hypocellular bone marrow, and episodic normal neutrophil count can be associated with SRP54 mutations causing Shwachman–Diamond-like syndrome 315
Pediatric immune myelofibrosis (PedIMF) as a novel and distinct clinical pathological entity 311
Primary immunodeficiencies, autoimmune hyperthyroidism, coeliac disease and systemic lupus erythematosus in childhood immune thrombocytopenia 298
A novel homozygous disruptive PRF1 variant (K285Sfs*4) causes very early-onset of familial hemophagocytic lymphohystiocytosis type 2 297
Early diagnosis of PI3Kδ syndrome in a 2 years old girl with recurrent otitis and enlarged spleen 289
Antibody Deficiency in Patients with Biallelic KARS1 Mutations 286
Abnormal B-Cell Maturation and Increased Transitional B Cells in CBL Syndrome 284
Secondary hemophagocytic lymphohystiocytosis in a Rubinstein Taybi syndrome patient 265
Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing Cholangitis 258
Ruptured hepatoblastoma: A case report and literature review 255
When to suspect GATA2 deficiency in pediatric patients: from complete blood count to diagnosis 255
More than an ‘atypical’ phenotype: dual molecular diagnosis of autoimmune lymphoproliferative syndrome and Becker muscular dystrophy 247
Neutropenia, hypogammaglobulinemia, and pneumonia: A case of WHIM syndrome 228
Hermansky-Pudlak syndrome type II and lethal hemophagocytic lymphohistiocytosis: Case description and review of the literature 228
Isolated leukopenia in children and adolescents referred to a Pediatric Hematology Clinic 227
Correction to: Antibody Deficiency in Patients with Biallelic KARS1 Mutations (Journal of Clinical Immunology, (2023), 43, 8, (2115-2125), 10.1007/s10875-023-01584-7) 223
Is multifocality a prognostic factor in childhood hepatoblastoma? 219
Finding balance between mature and immature neutrophils: The effects of empagliflozin in GSD-Ib 211
Identical EP300 variant leading to Rubinstein–Taybi syndrome with different clinical and immunologic phenotype 203
Bone Marrow CD8 + Abundance Inversely Correlates with Progressive Marrow Fibrosis and Myelodysplastic Evolution in GATA2 Deficiency: Case Report 200
Severe and recurrent infections identify severe congenital neutropenia and primary immunodeficiencies in pediatric isolated neutropenia 171
A novel germline mutation of ada2 gene in two “discordant” homozygous female twins affected by adenosine deaminase 2 deficiency: Description of the bone-related phenotype 170
SYNDROMES, GENETICS AND IMMUNOLOGY: FROM THE BEGINNING OF THE END TO THE END OF THE BEGINNING [Sindromi, genetica e immunologia: dall'inizio della fine alla fine dell'inizio] 169
Clinical features of Epstein-Barr virus infection in primary immunodeficiency patients 150
The novel XIAP Lys396Ter variant alters mitochondrial membrane potential and endoplasmic reticulum intensity in monocytes of two XIAP-deficient patients 131
Successful Treatment of Multirefractory Immune Thrombocytopenia in Rubinstein–Taybi Syndrome With Combined Rituximab and Eltrombopag 49
Totale 8.252
Categoria #
all - tutte 25.577
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 25.577


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022471 52 56 53 39 37 38 13 32 27 38 30 56
2022/2023588 56 188 26 65 32 77 9 46 51 5 16 17
2023/2024500 17 15 37 40 61 132 98 15 24 17 6 38
2024/20251.379 46 109 78 75 159 66 102 68 139 216 117 204
2025/20263.922 611 310 273 495 439 191 557 123 204 316 201 202
2026/2027126 126 0 0 0 0 0 0 0 0 0 0 0
Totale 8.252