IRIS
DA POZZO, PAOLA
 Distribuzione geografica
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Continente #
NA - Nord America 3.943
EU - Europa 2.642
AS - Asia 1.187
SA - Sud America 186
AF - Africa 56
Continente sconosciuto - Info sul continente non disponibili 55
OC - Oceania 5
Totale 8.074
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Nazione #
US - Stati Uniti d'America 3.898
GB - Regno Unito 673
RU - Federazione Russa 518
CN - Cina 463
SG - Singapore 360
IE - Irlanda 326
IT - Italia 280
SE - Svezia 192
UA - Ucraina 181
BR - Brasile 158
DE - Germania 149
FR - Francia 123
VN - Vietnam 104
FI - Finlandia 89
HK - Hong Kong 87
KR - Corea 48
ZA - Sudafrica 33
CA - Canada 26
IN - India 24
NL - Olanda 23
BE - Belgio 22
ES - Italia 19
TR - Turchia 18
BD - Bangladesh 16
AR - Argentina 13
CZ - Repubblica Ceca 11
IQ - Iraq 11
JP - Giappone 11
MX - Messico 10
PL - Polonia 8
NG - Nigeria 7
ID - Indonesia 6
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
HN - Honduras 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
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
RS - Serbia 1
SV - El Salvador 1
TT - Trinidad e Tobago 1
Totale 8.023
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Città #
Dallas 623
Southend 614
Menlo Park 523
Dublin 325
Ashburn 301
Fairfield 292
Chandler 193
Singapore 184
Jacksonville 151
Moscow 145
Santa Clara 145
Woodbridge 129
San Jose 127
Ann Arbor 124
Beijing 122
Wilmington 113
Seattle 108
Houston 105
Cambridge 93
Hong Kong 83
Milan 71
New York 63
Hefei 57
Princeton 57
The Dalles 57
Nanjing 54
Council Bluffs 51
Los Angeles 50
Seoul 48
Helsinki 43
Munich 40
Siena 40
Venezia 35
Ho Chi Minh City 34
Rome 33
Hanoi 31
Johannesburg 29
Boardman 28
Lauterbourg 27
Nanchang 25
San Mateo 22
Washington 21
Turku 17
Buffalo 16
Columbus 16
Shanghai 15
São Paulo 15
Izmir 14
Orem 14
San Diego 14
Tianjin 14
Florence 13
Brussels 12
Málaga 12
Shenyang 12
Tokyo 11
Kunming 10
Waanrode 10
Chennai 9
Hebei 9
Düsseldorf 8
Frankfurt am Main 8
Montreal 8
Brno 7
Jinan 7
London 7
Ningbo 7
Poplar 7
Abuja 6
Amsterdam 6
Changsha 6
Chicago 6
Haiphong 6
Rio de Janeiro 6
Warsaw 6
Bengaluru 5
Denver 5
Dhaka 5
Falls Church 5
Jakarta 5
Lancaster 5
Manchester 5
Naples 5
Norwalk 5
Redondo Beach 5
Stockholm 5
Aci Sant'Antonio 4
Belo Horizonte 4
Bishkek 4
Boston 4
Brooklyn 4
Figino 4
Itri 4
Jiaxing 4
North Bergen 4
Roubaix 4
San Francisco 4
Sofia 4
Toronto 4
Turin 4
Totale 5.861
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Nome #
A case of 3243A>G mutation in mtDNA presenting as apparently idiopathic hyperCKemia. 405
A novel heteroplasmic tRNA(Ser(UCN)) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss 393
A new thymidine phosphorylase mutation causing elongation of the protein underlies mitochondrial neurogastrointestinal encephalomyopathy 372
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients 348
A novel OPA1 mutation in a family with Autosomal Dominant Optic Atrophy 344
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy. 329
Frequency of OPA1 and OPTN gene variations in 18 patients with normal tension glaucoma 297
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families 290
Oxidative stress-induced apoptosis in peripheral blood lymphocytes from patients with POLG-related disorders 285
Sporadic myopathy, myoclonus, leukoencephalopathy, neurosensory deafness, hypertrophic cardiomyopathy and insulin resistance associated with the mitochondrial 8306 T>C MTTK mutation. 282
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy. 274
Alu-Element Insertion In The Opa1 Intron Sequence Associated With ADOA 267
Mitochondria, oxidative stress and neurodegeneration. 266
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene. 264
Alu-element insertion in the OPA1 intron sequence associated with ADOA 258
Genetic leukoencephalopaties with unknown metabolic pathogenesis 252
Molecular genetic study of Leber’s hereditary optic neurophaty (LHON): mutation screening by sequencing of ND1, ND4, ND%, ND6 genes 249
Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy 236
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telithromycin consumption 232
Commentary to mitDNA research for the pathogenesis of mitochondrial disorders. 223
Heterogeneity of retinal manifestations in mitochondrial myopathy: genotype/phenotype correlation in our experience. 220
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telythromicin consumption 217
Rapidly progressive neurodegeneration in a case with the 7472insC mutation and the A7472C polymorphism in the mtDNA tRNA ser(UCN) gene. 203
Leber hereditary optic neuropathy in 2 of 4 siblings with 11778 mtDNA mutation: clinical variability or effect of toxic exposure? 202
null 178
Sequence analysis of the complete mitochondrial genome in patients with mitochondrial encephaloneuromyopathies lacking the common pathogienic DNA mutations 177
possible founder mutation as the cause of adoa in the province of Syracuse, Sicily 155
Sporadic PEO caused by a novel POLG variation and a Twinkle mutation: digenic inheritance? 153
null 143
Erratum to: Redefining phenotypes associated with mitochondrial DNA single deletion 142
Mitochondrial recessive ataxia syndrome: A neurological rarity not to be missed. 129
null 111
null 89
Redefining phenotypes associated with mitochondrial DNA single deletion 89
Totale 8.074
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Categoria #
all - tutte 21.249
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 21.249
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022347 0 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
2025/20262.395 162 353 465 252 427 96 238 45 77 93 39 148
2026/2027133 88 45 0 0 0 0 0 0 0 0 0 0
Totale 8.074