DRERA, Bruno Angelo
 Distribuzione geografica
Continente #
NA - Nord America 480
EU - Europa 400
AS - Asia 124
AN - Antartide 1
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
SA - Sud America 1
Totale 1.008
Nazione #
US - Stati Uniti d'America 480
PL - Polonia 248
CN - Cina 68
UA - Ucraina 53
IT - Italia 21
DE - Germania 16
FR - Francia 16
HK - Hong Kong 14
SG - Singapore 14
TR - Turchia 14
FI - Finlandia 12
GB - Regno Unito 8
IE - Irlanda 8
VN - Vietnam 8
BE - Belgio 7
NL - Olanda 7
JP - Giappone 4
RU - Federazione Russa 4
ID - Indonesia 2
BR - Brasile 1
EU - Europa 1
GS - Georgia del Sud e Isole Sandwich Australi 1
NZ - Nuova Zelanda 1
Totale 1.008
Città #
Warsaw 248
Fairfield 75
Woodbridge 68
Houston 48
Jacksonville 38
Ann Arbor 33
Seattle 29
Ashburn 25
Cambridge 23
Chandler 23
Nanjing 23
Wilmington 23
Dearborn 17
Hong Kong 14
Princeton 14
Beijing 10
Singapore 10
Brescia 9
Dong Ket 8
Dublin 8
Istanbul 7
Kocaeli 6
Waanrode 6
Casalpusterlengo 5
Des Moines 5
Changsha 4
Helsinki 4
Kunming 4
New York 4
Shenyang 4
Jinan 3
Lancaster 3
Nanchang 3
Ferrara 2
Hangzhou 2
Hebei 2
Jakarta 2
San Diego 2
Tianjin 2
Zhengzhou 2
Brussels 1
Calusco d'Adda 1
Jiaxing 1
Lanzhou 1
Leawood 1
Milan 1
Moscow 1
Ningbo 1
San Francisco 1
Taiyuan 1
Taizhou 1
Tokyo 1
Verona 1
Totale 831
Nome #
Linee guida. Diagnosi delle epidermolisi bollose ereditarie. 214
Dystrophic epidermolysis bullosa pruriginosa in Italy: molecular characterization and pathogenesic aspects 171
Recurrence of the p.R156X TNNI2 mutation in distal arthrogryposis type 2B 125
Ischemic stroke in an adolescent with arterial tortuosity syndrome. 113
Branch point and donor splice-site COL7A1 mutations in mild recessive dystrophic epidermolysis bullosa. 112
De novo occurrence of the 730insG recurrent mutation in an Italian family with the ichthyotic variant of Vohwinkel syndrome, loricrin keratoderma. 109
Identification of a novel TGFBR1 mutation in a Loeys-Dietz syndrome type II patient with vascular Ehlers-Danlos syndrome phenotype 106
Modulation of the facilitative glucose transporters (SLC2A) gene family expression in arterial tortuosity syndrome skin fibroblasts and aortic vascular smooth muscle cells. 75
Totale 1.025
Categoria #
all - tutte 3.801
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 3.801


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020184 0 0 0 0 0 40 35 35 25 24 11 14
2020/2021153 7 15 12 17 9 14 5 19 21 14 9 11
2021/202261 3 23 0 1 0 0 5 2 2 5 6 14
2022/202371 6 0 0 1 9 21 0 2 14 0 4 14
2023/202441 8 3 4 1 0 4 0 0 14 0 1 6
2024/202534 0 0 0 19 11 4 0 0 0 0 0 0
Totale 1.025