BERNASCONI, Sergio
 Distribuzione geografica
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Continente #
NA - Nord America 1.071
EU - Europa 338
AS - Asia 123
AF - Africa 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 1.535
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Nazione #
US - Stati Uniti d'America 1.068
GB - Regno Unito 120
SE - Svezia 59
IT - Italia 47
HK - Hong Kong 40
DE - Germania 38
CN - Cina 37
SG - Singapore 22
UA - Ucraina 19
TR - Turchia 18
FI - Finlandia 13
FR - Francia 11
BG - Bulgaria 10
IE - Irlanda 6
NL - Olanda 4
CA - Canada 3
ID - Indonesia 3
LT - Lituania 3
CZ - Repubblica Ceca 2
EG - Egitto 2
ES - Italia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
IN - India 1
KH - Cambogia 1
MY - Malesia 1
NO - Norvegia 1
PL - Polonia 1
PT - Portogallo 1
RU - Federazione Russa 1
Totale 1.535
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Città #
Fairfield 199
Chandler 104
Woodbridge 104
Southend 89
Ashburn 81
Houston 79
Seattle 60
Cambridge 56
Nyköping 49
Wilmington 48
Dearborn 41
Hong Kong 40
Jacksonville 35
Ann Arbor 26
New York 25
San Diego 19
Bremen 14
Princeton 13
Singapore 13
Izmir 12
Beijing 11
Sofia 10
Eugene 9
Modena 9
Falls Church 8
Helsinki 8
London 7
Shanghai 7
Dublin 6
Norwalk 5
Kunming 4
Rio Saliceto 4
San Jose 4
Brescia 3
Hounslow 3
Jakarta 3
Leawood 3
Los Angeles 3
San Mateo 3
Santa Clara 3
Acton 2
Augusta 2
Boardman 2
Bologna 2
Brighton 2
Brno 2
Cairo 2
Chiswick 2
Kilburn 2
Lusciano 2
Paris 2
Rimini 2
Rome 2
Saint Louis 2
Secaucus 2
Segrate 2
Seville 2
Toronto 2
Wandsworth 2
Albuquerque 1
Berlin 1
Campi Bisenzio 1
Chicago 1
Florence 1
Formigine 1
Fremont 1
Guangzhou 1
Hanover 1
Islington 1
Las Vegas 1
Milan 1
Monmouth Junction 1
Munich 1
New Bedfont 1
Ningbo 1
Ottawa 1
Parma 1
Phnom Penh 1
Prescot 1
Roverbella 1
Shenzhen 1
Termoli 1
Trento 1
Usmate Velate 1
Totale 1.283
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Nome #
Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH) 238
Genotype/phenotype correlations of males affected by Simpson-Golabi-Behmel syndrome with GPC3 gene mutations: Patient report and review of the literature 176
VACTERL (vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, cardiac defects, renal and limb anomalies) association: disease spectrum in 25 patients ascertained for their upper limb involvement 173
Self-rectifying behavior and analog switching under identical pulses using Tri-layer RRAM crossbar array for neuromorphic systems 172
Relationship between body mass index and insulin measured during oral glucose tolerance testing in severely obese children and adolescents 169
Genetic basis of congenital upper limb anomalies: analysis of 487 cases of a specialized clinic 166
Mowat-Wilson syndrome: growth charts 104
Il gene SHOX e il suo ruolo nei disturbi dell’accrescimento 89
Clinical expression of endocrine disruptors in children 82
Pituitary Macroadenoma and Severe Hypothyroidism: The Link between Brain Imaging and Thyroid Function 64
A case report of female pseudohermaphroditism caused by maternal androluteoma 45
Diagnostic approach and therapy of overgrowth and tall stature in childhood 28
Insulin pulsatility in obese and normal prepubertal children 26
High prevalence of glucokinase mutations in Italian children with MODY. Influence on glucose tolerance, first-phase insulin response, insulin sensitivity and BMI 25
Totale 1.557
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Categoria #
all - tutte 7.203
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 7.203
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020272 0 10 16 25 26 47 54 27 29 8 16 14
2020/2021310 20 13 24 38 33 11 32 31 16 49 33 10
2021/2022261 43 33 21 18 4 16 12 14 18 10 48 24
2022/2023274 29 26 18 26 41 38 1 33 41 0 12 9
2023/2024188 3 10 9 27 42 14 8 36 9 3 10 17
2024/202518 12 6 0 0 0 0 0 0 0 0 0 0
Totale 1.557