CARROCCIA, ROSANNA
 Distribuzione geografica
Continente #
EU - Europa 221
NA - Nord America 219
AS - Asia 147
AF - Africa 11
Continente sconosciuto - Info sul continente non disponibili 1
Totale 599
Nazione #
US - Stati Uniti d'America 217
GB - Regno Unito 90
VN - Vietnam 58
CN - Cina 39
SE - Svezia 31
DE - Germania 30
SG - Singapore 28
IT - Italia 19
IN - India 14
IE - Irlanda 11
RU - Federazione Russa 9
FR - Francia 8
UA - Ucraina 8
CH - Svizzera 6
JO - Giordania 6
ZA - Sudafrica 5
EE - Estonia 4
TG - Togo 3
BG - Bulgaria 2
CA - Canada 2
CI - Costa d'Avorio 2
A2 - ???statistics.table.value.countryCode.A2??? 1
DK - Danimarca 1
FI - Finlandia 1
GR - Grecia 1
IR - Iran 1
LB - Libano 1
SC - Seychelles 1
Totale 599
Città #
Southend 85
Dong Ket 29
Santa Clara 29
Singapore 25
Chandler 24
Ashburn 16
Ann Arbor 14
Fairfield 12
Princeton 12
Dublin 11
Houston 11
Wilmington 8
Boardman 7
Amman 6
Jacksonville 6
Padova 6
Seattle 6
Westminster 6
Berlin 5
Guangzhou 5
Medford 5
Nanjing 5
Woodbridge 5
Bern 4
Hebei 4
Nanchang 4
Cambridge 3
Jiaxing 3
Lomé 3
Saint Petersburg 3
Shanghai 3
Shenyang 3
Abidjan 2
Dalmine 2
Falkenstein 2
Falls Church 2
Florence 2
Milan 2
New York 2
Qingdao 2
Sofia 2
Turin 2
Ardabil 1
Beijing 1
Bologna 1
Braunschweig 1
Bremen 1
Chengdu 1
Dearborn 1
Dongguan 1
Foshan 1
Frankfurt am Main 1
Haikou 1
Hangzhou 1
Helsinki 1
Leawood 1
Los Angeles 1
Mahé 1
Ningbo 1
Phoenix 1
Pune 1
Racine 1
Tianjin 1
Toronto 1
Vancouver 1
Verona 1
Washington 1
Totale 413
Nome #
A new case of Sando syndrome and retinitis pigmentosa with novel combination of compound heterozygous POLG mutations. 163
Mitochondrial optic neuropathies: how two genomes may kill the same cell type? 139
Extreme variability in genotype/phenotype correlation in an Italian family carrying the mtDNA A3243G/tRNALeu(UUR) MELAS mutation. 89
"Plus" features of Leber's Hereditary Optic Neuropathy in nineteen Italian families. 82
Myopathy and retinopathy are novel features in a patient with Mohr-Tranebjaerg syndrome. 67
Extraocular Clinical Features in Leber's Hereditary Optic Neuropathy (LHON) Italian Families. 66
OPA1 mutations induce mitochondrial DNA instability and optic atrophy plus phenotypes 9
Totale 615
Categoria #
all - tutte 1.606
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 1.606


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202053 0 0 0 0 0 0 7 15 19 3 3 6
2020/202179 16 3 0 7 6 2 1 4 1 1 3 35
2021/2022137 35 7 3 3 10 4 4 3 4 15 27 22
2022/2023115 13 22 8 9 4 10 3 7 21 1 6 11
2023/202433 1 4 2 6 2 8 3 1 0 2 0 4
2024/202584 6 13 13 2 47 3 0 0 0 0 0 0
Totale 615