DE TONI, TERESINA
 Distribuzione geografica
Continente #
EU - Europa 1.745
AS - Asia 170
NA - Nord America 38
SA - Sud America 16
AF - Africa 2
Totale 1.971
Nazione #
IT - Italia 1.721
SG - Singapore 68
CN - Cina 48
VN - Vietnam 36
US - Stati Uniti d'America 34
FR - Francia 11
AR - Argentina 8
BR - Brasile 5
HK - Hong Kong 5
CH - Svizzera 4
FI - Finlandia 4
JP - Giappone 4
DE - Germania 3
AE - Emirati Arabi Uniti 2
EC - Ecuador 2
ID - Indonesia 2
MX - Messico 2
ZA - Sudafrica 2
BD - Bangladesh 1
CA - Canada 1
CO - Colombia 1
IN - India 1
IQ - Iraq 1
JM - Giamaica 1
NL - Olanda 1
PS - Palestinian Territory 1
RU - Federazione Russa 1
SA - Arabia Saudita 1
Totale 1.971
Città #
Genova 1.125
Genoa 346
Rapallo 133
Vado Ligure 102
Singapore 27
San Jose 14
Ho Chi Minh City 13
Lauterbourg 11
Beijing 8
Hanoi 8
Guangzhou 5
Hong Kong 5
Ashburn 4
Helsinki 4
Santa Clara 4
Tokyo 4
Zurich 4
Bordighera 3
Da Nang 3
Frankfurt am Main 3
Venice 3
Orem 2
Tây Ninh 2
Acalanes Ridge 1
Ajman 1
Alpestre 1
Amsterdam 1
Apodaca 1
Araruama 1
Atlanta 1
Baghdad 1
Berrotarán 1
Bologna 1
Canoas 1
Cape Town 1
Changsha 1
Dammam 1
Des Moines 1
Dubai 1
Gresik 1
Guayaquil 1
Haiphong 1
Hyderabad 1
Johannesburg 1
José C. Paz 1
Kingston 1
Laferrere 1
Lumajang 1
Manchester 1
Matelica 1
Mexico City 1
Milan 1
Monte Grande 1
Natal 1
New York 1
Nha Trang 1
Orenburg 1
Ottawa 1
Paltan 1
Panama City Beach 1
Phủ Lý 1
Puerto Iguazú 1
Quito 1
Quảng Ngãi 1
Rome 1
San Donà di Piave 1
San Luis 1
Saravena 1
São Paulo 1
Thái Nguyên 1
Tianjin 1
Veroli 1
Vicente López 1
Totale 1.883
Nome #
PITUITARY HYPOPLASIA AND GROWTH HORMONE DEFICIENCY IN COFFIN-SIRIS SYNDROME 179
The Italian National Survey for Prader-Willi syndrome: an epidemiologic study. 177
A survey on Prader-Willi syndrome in the Italian population: prevalence of historical and clinical signs. 169
Wolfram syndrome (diabetes insipidus, diabetes, optic atrophy, and deafness): clinical and genetic study. 168
Clinical and genetic characterization of Chanarin-Dorfman syndrome 163
Further case of metaphyseal acroscyphodysplasia with cone-shaped epiphyses (Bellini disease or metaphyseal dyschondroplasia). 159
Growth hormone secretory pattern in non-obese children and adolescents with Prader-Willi syndrome 154
Growth hormone secretory pattern in non-obese children and adolescents with Prader-Willi syndrome. 148
Due casi di difficile inquadramento: coreoatetosi e sordità in fratelli 142
Coffin-Siris syndrome and the BAF complex: genotype-phenotype study in 63 patients. 140
A novel Xp22.11 deletion causing a syndrome of craniosynostosis and periventricular nodular heterotopia. 132
Clinical and cytogenetic study of a case of trisomy 1q with familial translocation t(1;5)(q42;p15.3) 130
Adolescenza. Verso un approccio multidisciplinare 110
Totale 1.971
Categoria #
all - tutte 5.539
article - articoli 5.178
book - libri 0
conference - conferenze 0
curatela - curatele 361
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 11.078


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202122 0 0 0 0 0 0 0 0 0 11 5 6
2021/2022166 5 18 4 17 13 11 12 41 5 15 7 18
2022/2023168 18 20 9 15 17 27 1 15 13 0 30 3
2023/202486 4 17 1 14 12 8 6 4 3 5 3 9
2024/2025203 6 17 10 18 28 25 11 26 10 9 21 22
2025/2026389 82 9 16 26 92 23 65 18 27 31 0 0
Totale 1.971