IRIS
DA POZZO, PAOLA
 Distribuzione geografica
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Continente #
NA - Nord America 3.742
EU - Europa 2.511
AS - Asia 1.183
SA - Sud America 184
AF - Africa 56
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 4
Totale 7.685
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Nazione #
US - Stati Uniti d'America 3.700
GB - Regno Unito 673
RU - Federazione Russa 518
CN - Cina 463
SG - Singapore 359
IE - Irlanda 326
SE - Svezia 181
UA - Ucraina 181
IT - Italia 161
BR - Brasile 157
DE - Germania 149
FR - Francia 123
VN - Vietnam 103
FI - Finlandia 89
HK - Hong Kong 86
KR - Corea 48
ZA - Sudafrica 33
CA - Canada 24
IN - India 24
NL - Olanda 23
BE - Belgio 22
ES - Italia 19
TR - Turchia 18
BD - Bangladesh 16
AR - Argentina 12
CZ - Repubblica Ceca 11
IQ - Iraq 11
JP - Giappone 11
MX - Messico 10
PL - Polonia 8
NG - Nigeria 7
ID - Indonesia 5
SA - Arabia Saudita 5
BG - Bulgaria 4
EC - Ecuador 4
KG - Kirghizistan 4
PK - Pakistan 4
AU - Australia 3
CL - Cile 3
EG - Egitto 3
EU - Europa 3
IR - Iran 3
LT - Lituania 3
RO - Romania 3
SN - Senegal 3
UZ - Uzbekistan 3
VE - Venezuela 3
AL - Albania 2
AO - Angola 2
AT - Austria 2
CY - Cipro 2
DZ - Algeria 2
GR - Grecia 2
HR - Croazia 2
IL - Israele 2
KZ - Kazakistan 2
LK - Sri Lanka 2
LV - Lettonia 2
MA - Marocco 2
NZ - Nuova Zelanda 2
PH - Filippine 2
PT - Portogallo 2
TN - Tunisia 2
UY - Uruguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
AN - Antille olandesi 1
BO - Bolivia 1
CH - Svizzera 1
CI - Costa d'Avorio 1
CO - Colombia 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GL - Groenlandia 1
HN - Honduras 1
HU - Ungheria 1
JM - Giamaica 1
JO - Giordania 1
KW - Kuwait 1
LB - Libano 1
LU - Lussemburgo 1
MD - Moldavia 1
MM - Myanmar 1
MY - Malesia 1
NP - Nepal 1
OM - Oman 1
PR - Porto Rico 1
PS - Palestinian Territory 1
PY - Paraguay 1
QA - Qatar 1
SV - El Salvador 1
TT - Trinidad e Tobago 1
Totale 7.685
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Città #
Dallas 623
Southend 614
Menlo Park 523
Dublin 325
Fairfield 292
Ashburn 277
Chandler 193
Singapore 184
Jacksonville 150
Moscow 145
Woodbridge 129
Santa Clara 127
Beijing 122
Ann Arbor 116
Wilmington 113
Seattle 108
Houston 105
Cambridge 93
Hong Kong 82
San Jose 81
New York 62
Hefei 57
Princeton 57
The Dalles 57
Nanjing 54
Los Angeles 48
Seoul 48
Helsinki 43
Munich 40
Siena 40
Venezia 35
Ho Chi Minh City 33
Hanoi 31
Johannesburg 29
Boardman 27
Lauterbourg 27
Nanchang 25
San Mateo 22
Washington 21
Council Bluffs 17
Turku 17
Buffalo 16
Shanghai 15
São Paulo 15
Izmir 14
Orem 14
San Diego 14
Tianjin 14
Brussels 12
Florence 12
Málaga 12
Shenyang 12
Columbus 11
Tokyo 11
Kunming 10
Rome 10
Waanrode 10
Chennai 9
Hebei 9
Düsseldorf 8
Frankfurt am Main 8
Montreal 8
Brno 7
Jinan 7
Ningbo 7
Poplar 7
Abuja 6
Amsterdam 6
Changsha 6
Chicago 6
Haiphong 6
London 6
Rio de Janeiro 6
Warsaw 6
Bengaluru 5
Denver 5
Dhaka 5
Falls Church 5
Lancaster 5
Manchester 5
Milan 5
Norwalk 5
Redondo Beach 5
Stockholm 5
Aci Sant'Antonio 4
Belo Horizonte 4
Bishkek 4
Boston 4
Itri 4
Jakarta 4
Jiaxing 4
Roubaix 4
San Francisco 4
Sofia 4
Toronto 4
Atlanta 3
Auburn Hills 3
Bexley 3
Biên Hòa 3
Brasília 3
Totale 5.621
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Nome #
A case of 3243A>G mutation in mtDNA presenting as apparently idiopathic hyperCKemia. 390
A novel heteroplasmic tRNA(Ser(UCN)) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss 378
A new thymidine phosphorylase mutation causing elongation of the protein underlies mitochondrial neurogastrointestinal encephalomyopathy 361
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients 339
A novel OPA1 mutation in a family with Autosomal Dominant Optic Atrophy 326
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy. 320
Frequency of OPA1 and OPTN gene variations in 18 patients with normal tension glaucoma 284
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families 277
Oxidative stress-induced apoptosis in peripheral blood lymphocytes from patients with POLG-related disorders 275
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy. 266
Sporadic myopathy, myoclonus, leukoencephalopathy, neurosensory deafness, hypertrophic cardiomyopathy and insulin resistance associated with the mitochondrial 8306 T>C MTTK mutation. 261
Alu-Element Insertion In The Opa1 Intron Sequence Associated With ADOA 254
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene. 253
Mitochondria, oxidative stress and neurodegeneration. 247
Genetic leukoencephalopaties with unknown metabolic pathogenesis 245
Alu-element insertion in the OPA1 intron sequence associated with ADOA. 243
Molecular genetic study of Leber’s hereditary optic neurophaty (LHON): mutation screening by sequencing of ND1, ND4, ND%, ND6 genes 238
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telithromycin consumption 228
Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy 228
Commentary to mitDNA research for the pathogenesis of mitochondrial disorders. 216
Heterogeneity of retinal manifestations in mitochondrial myopathy: genotype/phenotype correlation in our experience. 207
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telythromicin consumption 204
Leber hereditary optic neuropathy in 2 of 4 siblings with 11778 mtDNA mutation: clinical variability or effect of toxic exposure? 197
Rapidly progressive neurodegeneration in a case with the 7472insC mutation and the A7472C polymorphism in the mtDNA tRNA ser(UCN) gene. 188
null 178
Sequence analysis of the complete mitochondrial genome in patients with mitochondrial encephaloneuromyopathies lacking the common pathogienic DNA mutations 171
possible founder mutation as the cause of adoa in the province of Syracuse, Sicily 145
null 143
Sporadic PEO caused by a novel POLG variation and a Twinkle mutation: digenic inheritance? 141
Erratum to: Redefining phenotypes associated with mitochondrial DNA single deletion 129
Mitochondrial recessive ataxia syndrome: A neurological rarity not to be missed. 118
null 111
null 89
Redefining phenotypes associated with mitochondrial DNA single deletion 86
Totale 7.736
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Categoria #
all - tutte 19.684
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 19.684
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021135 0 0 0 0 0 0 0 0 0 35 74 26
2021/2022373 26 52 24 29 23 14 26 9 17 38 39 76
2022/2023645 36 52 110 79 66 123 10 55 56 15 17 26
2023/2024591 17 6 66 24 41 189 186 13 4 8 1 36
2024/2025938 12 54 86 41 130 48 27 66 94 31 108 241
2025/20262.190 162 353 465 252 427 96 238 45 77 75 0 0
Totale 7.736