VENTURI, Giacomo
 Distribuzione geografica
Continente #
NA - Nord America 682
EU - Europa 583
AS - Asia 258
SA - Sud America 4
AF - Africa 1
Totale 1.528
Nazione #
US - Stati Uniti d'America 679
GB - Regno Unito 225
CN - Cina 157
SE - Svezia 70
SG - Singapore 58
IT - Italia 51
IE - Irlanda 48
FI - Finlandia 46
RU - Federazione Russa 43
DE - Germania 37
FR - Francia 35
TR - Turchia 15
UA - Ucraina 9
VN - Vietnam 7
BE - Belgio 5
ID - Indonesia 5
JP - Giappone 5
NL - Olanda 5
KR - Corea 3
LV - Lettonia 3
AE - Emirati Arabi Uniti 2
CA - Canada 2
IN - India 2
PE - Perù 2
BG - Bulgaria 1
BO - Bolivia 1
BR - Brasile 1
CZ - Repubblica Ceca 1
ES - Italia 1
GR - Grecia 1
HK - Hong Kong 1
IM - Isola di Man 1
IQ - Iraq 1
JM - Giamaica 1
MA - Marocco 1
PK - Pakistan 1
RO - Romania 1
SA - Arabia Saudita 1
Totale 1.528
Città #
Southend 195
Chandler 140
Jacksonville 120
Woodbridge 67
Houston 51
Singapore 50
Dublin 48
Ashburn 47
Ann Arbor 35
Verona 33
New York 22
Lancaster 18
Beijing 17
Jinan 17
Nanjing 17
Wilmington 17
Lawrence 16
Princeton 16
Helsinki 13
Shenyang 13
Sindelfingen 11
Haikou 8
Jiaxing 7
Los Angeles 7
Tianjin 7
Ningbo 6
Brussels 5
Dong Ket 5
Hangzhou 5
Jakarta 5
Tokyo 5
Hebei 4
Lanzhou 4
Nanchang 4
Taizhou 4
Zhengzhou 4
Auburn Hills 3
Boardman 3
Changsha 3
Fairfield 3
Guangzhou 3
Milan 3
Seoul 3
Taiyuan 3
Washington 3
Bologna 2
Clearwater 2
Lima 2
Moscow 2
Newark 2
Norwalk 2
Redwood City 2
Riga 2
San Francisco 2
Sanayi 2
Venice 2
Athens 1
Brasov 1
Caprino Bergamasco 1
Chicago 1
Clifton 1
Dallas 1
Delhi 1
Douglas 1
Dubai 1
Düsseldorf 1
Fuzhou 1
Groningen 1
Islamabad 1
Kemerovo 1
Lappeenranta 1
Leawood 1
Lincoln 1
Madrid 1
Munich 1
Olomouc 1
Phoenix 1
Puxian 1
Rabat 1
Riva 1
Riyadh 1
Saint Louis 1
San Martino Buon Albergo 1
Santa Clara 1
Shijiazhuang 1
Sofia 1
Sucre 1
Toronto 1
Xiangfen 1
Totale 1.125
Nome #
Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen 130
A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defect 125
A Novel Splicing Mutation in FKBP10 in a patient with a moderate Osteogenesis Imperfecta histologically classificable as type VI 115
Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I 112
Growth Hormone in Combination with Bisphosphonate Treatment in Osteogenesis Imperfecta. 109
The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene 104
How to cope with a severe skeletal dysplasia 100
Molecular screening in OI patients at Verona reference center: typical mutations 90
Osteogenesis Imperfecta: clinical, biochemical and molecular findings 90
Novel Splicing Mutation in FKBP10 gene in a patient with moderate-severe form of Osteogenesis imperfecta 87
Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism 87
Hypercalciuria and renal function in children affected by Osteogenesis Imperfecta 85
No osteonecrosis of the jaw in children and adolescents treated with Neridronate for osteogenesis imperfecta. 84
Osteogenesis imperfecta and its molecular diagnosis by determination of mutations of type I collagen genes 78
GH in combination with bisphosphonate treatment in osteogenesis imperfecta 77
Current and emerging treatments for the management of osteogenesis imperfecta 69
Totale 1.542
Categoria #
all - tutte 4.650
article - articoli 2.353
book - libri 0
conference - conferenze 2.297
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 9.300


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202094 0 0 0 0 13 10 20 15 2 16 7 11
2020/2021166 16 30 20 10 25 15 3 15 13 0 11 8
2021/2022146 18 42 1 22 1 3 0 4 7 3 11 34
2022/2023317 20 47 33 59 30 70 8 9 31 1 5 4
2023/2024182 8 10 27 16 19 39 2 7 0 13 30 11
2024/2025147 15 22 24 77 9 0 0 0 0 0 0 0
Totale 1.542