CORTI, PAOLA CONSUELO
 Distribuzione geografica
Continente #
NA - Nord America 676
EU - Europa 254
AS - Asia 58
SA - Sud America 5
AF - Africa 1
Totale 994
Nazione #
US - Stati Uniti d'America 668
DE - Germania 87
SE - Svezia 54
IT - Italia 44
CN - Cina 42
GB - Regno Unito 18
BE - Belgio 13
UA - Ucraina 13
CA - Canada 8
FI - Finlandia 8
IE - Irlanda 8
BR - Brasile 5
IN - India 5
VN - Vietnam 5
DK - Danimarca 4
TR - Turchia 3
BG - Bulgaria 2
IR - Iran 2
EG - Egitto 1
FR - Francia 1
KR - Corea 1
RO - Romania 1
RU - Federazione Russa 1
Totale 994
Città #
Ann Arbor 169
Chandler 71
Fairfield 71
Woodbridge 58
Wilmington 57
Frankfurt am Main 48
Houston 41
Ashburn 31
Cambridge 27
Seattle 26
Princeton 16
Dearborn 15
Brussels 13
Beijing 12
Jacksonville 12
Milan 11
Dublin 8
Fremont 8
Lawrence 8
Dong Ket 5
Helsinki 5
Lissone 5
Nanjing 5
Shanghai 5
Altamura 4
San Diego 4
Hebei 3
Nürnberg 3
Ottawa 3
Boardman 2
Grafing 2
Guangzhou 2
Jiaxing 2
Kunming 2
Lachine 2
Monza 2
Nanchang 2
Plovdiv 2
Rome 2
San Mateo 2
Saronno 2
Toronto 2
Zanjan 2
Catania 1
Contursi 1
Edmonton 1
Esslingen am Neckar 1
Florence 1
Hanover 1
Jinan 1
Kiev 1
Kocaeli 1
Lappeenranta 1
London 1
Merate 1
Nardò 1
New Bedfont 1
Ningbo 1
Roda 1
Sacramento 1
San Giuliano Milanese 1
San Jose 1
Seoul 1
Shenyang 1
Taiyuan 1
Taizhou 1
Velletri 1
Weimar 1
Wenzhou 1
Totale 798
Nome #
Mesenchymal stromal cells from Shwachman-Diamond syndrome patients fail to recreate a bone marrow niche in vivo and exhibit impaired angiogenesis 217
Human aplastic anaemia-derived mesenchymal stromal cells form functional haematopoietic stem cell niche in vivo 185
Intermittent granulocyte maturation arrest, hypocellular bone marrow, and episodic normal neutrophil count can be associated with SRP54 mutations causing Shwachman–Diamond-like syndrome 143
Bath PUVA therapy in pediatric patients with drug-resistant cutaneous graft-versus-host disease 138
Heterozygous mutation in adenosine deaminase gene in a patient with severe lymphopenia following corticosteroid treatment of autoimmune hemolytic anemia 133
More than an ‘atypical’ phenotype: dual molecular diagnosis of autoimmune lymphoproliferative syndrome and Becker muscular dystrophy 97
Rituximab Unveils Hypogammaglobulinemia and Immunodeficiency in Children with Autoimmune Cytopenia 75
Secondary hemophagocytic lymphohystiocytosis in a Rubinstein Taybi syndrome patient 59
Pediatric immune myelofibrosis (PedIMF) as a novel and distinct clinical pathological entity 18
Totale 1.065
Categoria #
all - tutte 2.392
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 2.392


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201984 0 0 1 1 0 6 3 2 5 9 26 31
2019/2020247 23 17 12 21 21 34 31 19 20 20 15 14
2020/2021257 7 16 18 41 20 25 22 33 22 24 6 23
2021/2022123 15 4 15 4 9 12 2 9 11 12 12 18
2022/2023250 19 77 13 28 12 37 7 22 20 7 0 8
2023/202433 9 4 20 0 0 0 0 0 0 0 0 0
Totale 1.065