VENTURI, Giacomo
 Distribuzione geografica
Continente #
NA - Nord America 652
EU - Europa 550
AS - Asia 189
SA - Sud America 4
AF - Africa 1
Totale 1.396
Nazione #
US - Stati Uniti d'America 650
GB - Regno Unito 225
CN - Cina 138
SE - Svezia 70
IT - Italia 49
IE - Irlanda 48
FI - Finlandia 46
DE - Germania 36
FR - Francia 35
RU - Federazione Russa 15
TR - Turchia 15
SG - Singapore 14
UA - Ucraina 9
VN - Vietnam 7
BE - Belgio 5
JP - Giappone 5
NL - Olanda 5
KR - Corea 3
LV - Lettonia 3
AE - Emirati Arabi Uniti 2
CA - Canada 2
PE - Perù 2
BG - Bulgaria 1
BO - Bolivia 1
BR - Brasile 1
CZ - Repubblica Ceca 1
HK - Hong Kong 1
IM - Isola di Man 1
IN - India 1
IQ - Iraq 1
MA - Marocco 1
PK - Pakistan 1
RO - Romania 1
SA - Arabia Saudita 1
Totale 1.396
Città #
Southend 195
Chandler 140
Jacksonville 120
Woodbridge 67
Houston 51
Dublin 48
Ashburn 41
Ann Arbor 35
Verona 31
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
Singapore 8
Jiaxing 7
Tianjin 7
Ningbo 6
Brussels 5
Dong Ket 5
Hangzhou 5
Los Angeles 5
Tokyo 5
Hebei 4
Lanzhou 4
Nanchang 4
Taizhou 4
Zhengzhou 4
Auburn Hills 3
Boardman 3
Changsha 3
Fairfield 3
Milan 3
Seoul 3
Taiyuan 3
Washington 3
Bologna 2
Clearwater 2
Guangzhou 2
Lima 2
Norwalk 2
Redwood City 2
Riga 2
San Francisco 2
Sanayi 2
Venice 2
Brasov 1
Caprino Bergamasco 1
Chicago 1
Clifton 1
Douglas 1
Dubai 1
Düsseldorf 1
Fuzhou 1
Groningen 1
Islamabad 1
Kemerovo 1
Lappeenranta 1
Leawood 1
Lincoln 1
Moscow 1
Newark 1
Olomouc 1
Phoenix 1
Puxian 1
Rabat 1
Riva 1
Riyadh 1
Saint Louis 1
San Martino Buon Albergo 1
Sofia 1
Sucre 1
Toronto 1
Xiangfen 1
Totale 1.058
Nome #
Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen 121
A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defect 115
A Novel Splicing Mutation in FKBP10 in a patient with a moderate Osteogenesis Imperfecta histologically classificable as type VI 107
Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I 103
Growth Hormone in Combination with Bisphosphonate Treatment in Osteogenesis Imperfecta. 101
The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene 94
How to cope with a severe skeletal dysplasia 92
Osteogenesis Imperfecta: clinical, biochemical and molecular findings 83
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 80
Molecular screening in OI patients at Verona reference center: typical mutations 78
No osteonecrosis of the jaw in children and adolescents treated with Neridronate for osteogenesis imperfecta. 78
Hypercalciuria and renal function in children affected by Osteogenesis Imperfecta 77
Novel Splicing Mutation in FKBP10 gene in a patient with moderate-severe form of Osteogenesis imperfecta 77
Osteogenesis imperfecta and its molecular diagnosis by determination of mutations of type I collagen genes 71
GH in combination with bisphosphonate treatment in osteogenesis imperfecta 70
Current and emerging treatments for the management of osteogenesis imperfecta 63
Totale 1.410
Categoria #
all - tutte 3.980
article - articoli 1.998
book - libri 0
conference - conferenze 1.982
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 7.960


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020130 20 0 1 15 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
2024/202515 15 0 0 0 0 0 0 0 0 0 0 0
Totale 1.410