RAVANI, Anna
 Distribuzione geografica
Continente #
NA - Nord America 612
EU - Europa 155
AS - Asia 121
SA - Sud America 4
Totale 892
Nazione #
US - Stati Uniti d'America 610
CN - Cina 58
SG - Singapore 42
DE - Germania 37
IT - Italia 31
UA - Ucraina 24
GB - Regno Unito 18
FI - Finlandia 13
SE - Svezia 12
TR - Turchia 9
BE - Belgio 5
LT - Lituania 5
VN - Vietnam 5
ID - Indonesia 4
AT - Austria 3
CZ - Repubblica Ceca 3
BR - Brasile 2
NL - Olanda 2
CA - Canada 1
CL - Cile 1
CO - Colombia 1
CY - Cipro 1
IN - India 1
LI - Liechtenstein 1
MX - Messico 1
MY - Malesia 1
RO - Romania 1
Totale 892
Città #
Fairfield 79
Chandler 62
Woodbridge 55
Ashburn 49
Houston 46
Singapore 38
Santa Clara 34
Ann Arbor 32
Jacksonville 31
Cambridge 28
Seattle 25
Wilmington 24
New York 16
Beijing 14
Milan 13
Shanghai 13
Munich 11
Bremen 9
Izmir 9
Princeton 9
Nanjing 8
Boardman 7
Helsinki 6
Nanchang 6
Brussels 5
Ferrara 4
Jakarta 4
Los Angeles 4
San Diego 4
Dearborn 3
Jiaxing 3
London 3
Washington 3
Auburn Hills 2
Changsha 2
Des Moines 2
Dong Ket 2
Gradara 2
Hebei 2
Padova 2
Trieste 2
Vreden 2
Addison 1
Americana 1
Amsterdam 1
Andover 1
Bologna 1
Brno 1
Bucharest 1
Clifton 1
Edinburgh 1
Falls Church 1
Foggia 1
Gubbio 1
Haikou 1
Hanoi 1
Ho Chi Minh City 1
Hyderabad 1
Indiana 1
Islington 1
Jinan 1
Kuala Lumpur 1
Kunming 1
Lappeenranta 1
Limassol 1
Medellín 1
Modena 1
Monmouth Junction 1
Mountain View 1
Nantong 1
Norwalk 1
Olomouc 1
Orange 1
Ottawa 1
Prague 1
Redwood City 1
Shenyang 1
São Paulo 1
Tianjin 1
Vaduz 1
Veracruz 1
Wenzhou 1
Yellow Springs 1
Zhengzhou 1
Totale 717
Nome #
GENETIC, CLINICAL AND NEUROPATHOLOGICAL INSIGHTS INTO PATIENTS WITH ASCERTAINED DIAGNOSIS OF HUNTINGTON DISEASE 122
Characterization of Hb Calvino (HBB: c.406G > A): A New Silent β-Globin Gene Variant Found in Coexistence with α-Thalassemia in a Family of African Origin 120
Genetic counseling for women referred for advanced maternal age: a telegenetic approach 119
A Family with γ-Thalassemia and High Hb A2 Levels 118
Novel mutations in the SLC26A4 gene 109
Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcript 88
Universal neonatal screening for sickle cell disease and other haemoglobinopathies in Ferrara, Italy 87
Workload measurement for molecular genetics laboratory: A survey study 71
Can paranasal sinus computed tomography screen for cystic fibrosis heterozygotes? 51
Ion concentrations in nasal airway surface liquid: a prediction model for the identification of cystic fibrosis carriers 28
Totale 913
Categoria #
all - tutte 5.447
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 5.447


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020118 0 0 0 0 0 22 19 17 14 32 11 3
2020/202187 8 6 1 13 2 7 6 8 3 8 18 7
2021/202294 9 4 0 11 1 7 1 7 4 7 6 37
2022/2023128 10 17 4 15 22 17 12 12 11 0 8 0
2023/202489 5 11 4 1 4 32 4 6 0 1 0 21
2024/2025128 4 8 24 11 49 32 0 0 0 0 0 0
Totale 913