RAVANI, Anna
 Distribuzione geografica
Continente #
NA - Nord America 599
EU - Europa 144
AS - Asia 117
SA - Sud America 4
Totale 864
Nazione #
US - Stati Uniti d'America 597
CN - Cina 57
SG - Singapore 39
DE - Germania 34
IT - Italia 31
UA - Ucraina 24
GB - Regno Unito 18
SE - Svezia 12
TR - Turchia 9
FI - Finlandia 8
VN - Vietnam 5
BE - Belgio 4
ID - Indonesia 4
LT - Lituania 4
AT - Austria 3
BR - Brasile 2
CZ - Repubblica Ceca 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 864
Città #
Fairfield 79
Chandler 62
Woodbridge 55
Ashburn 49
Houston 46
Singapore 35
Ann Arbor 32
Jacksonville 31
Cambridge 28
Seattle 25
Wilmington 24
Santa Clara 21
New York 16
Beijing 14
Milan 13
Shanghai 13
Bremen 9
Izmir 9
Princeton 9
Munich 8
Nanjing 8
Boardman 7
Nanchang 6
Brussels 4
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
Helsinki 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
Norwalk 1
Olomouc 1
Orange 1
Ottawa 1
Redwood City 1
Shenyang 1
São Paulo 1
Tianjin 1
Vaduz 1
Veracruz 1
Wenzhou 1
Yellow Springs 1
Zhengzhou 1
Totale 690
Nome #
GENETIC, CLINICAL AND NEUROPATHOLOGICAL INSIGHTS INTO PATIENTS WITH ASCERTAINED DIAGNOSIS OF HUNTINGTON DISEASE 121
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 117
A Family with γ-Thalassemia and High Hb A2 Levels 116
Genetic counseling for women referred for advanced maternal age: a telegenetic approach 116
Novel mutations in the SLC26A4 gene 106
Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcript 87
Universal neonatal screening for sickle cell disease and other haemoglobinopathies in Ferrara, Italy 79
Workload measurement for molecular genetics laboratory: A survey study 67
Can paranasal sinus computed tomography screen for cystic fibrosis heterozygotes? 50
Ion concentrations in nasal airway surface liquid: a prediction model for the identification of cystic fibrosis carriers 26
Totale 885
Categoria #
all - tutte 5.309
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 5.309


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
2024/2025100 4 8 24 11 49 4 0 0 0 0 0 0
Totale 885