IRIS
DA POZZO, PAOLA
 Distribuzione geografica
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Continente #
NA - Nord America 4.178
EU - Europa 2.664
AS - Asia 1.200
SA - Sud America 196
AF - Africa 59
Continente sconosciuto - Info sul continente non disponibili 56
OC - Oceania 6
Totale 8.359
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Nazione #
US - Stati Uniti d'America 4.116
GB - Regno Unito 677
RU - Federazione Russa 520
CN - Cina 466
SG - Singapore 362
IE - Irlanda 326
IT - Italia 286
SE - Svezia 196
UA - Ucraina 182
BR - Brasile 160
DE - Germania 149
FR - Francia 127
VN - Vietnam 104
FI - Finlandia 89
HK - Hong Kong 87
KR - Corea 48
ZA - Sudafrica 34
CA - Canada 33
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
EC - Ecuador 9
PL - Polonia 8
IL - Israele 7
NG - Nigeria 7
ID - Indonesia 6
SA - Arabia Saudita 5
AU - Australia 4
BG - Bulgaria 4
HN - Honduras 4
KG - Kirghizistan 4
PK - Pakistan 4
VE - Venezuela 4
CL - Cile 3
CO - Colombia 3
EG - Egitto 3
EU - Europa 3
GT - Guatemala 3
IR - Iran 3
JM - Giamaica 3
LT - Lituania 3
MY - Malesia 3
RO - Romania 3
SN - Senegal 3
SV - El Salvador 3
UZ - Uzbekistan 3
AL - Albania 2
AO - Angola 2
AT - Austria 2
CY - Cipro 2
DZ - Algeria 2
GR - Grecia 2
HR - Croazia 2
KZ - Kazakistan 2
LK - Sri Lanka 2
LV - Lettonia 2
MA - Marocco 2
NZ - Nuova Zelanda 2
PH - Filippine 2
PT - Portogallo 2
SC - Seychelles 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
CW - ???statistics.table.value.countryCode.CW??? 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EE - Estonia 1
ET - Etiopia 1
GL - Groenlandia 1
HU - Ungheria 1
JO - Giordania 1
KW - Kuwait 1
LB - Libano 1
LU - Lussemburgo 1
MD - Moldavia 1
MM - Myanmar 1
NI - Nicaragua 1
NP - Nepal 1
OM - Oman 1
PR - Porto Rico 1
PS - Palestinian Territory 1
PY - Paraguay 1
QA - Qatar 1
RS - Serbia 1
SY - Repubblica araba siriana 1
TT - Trinidad e Tobago 1
Totale 8.308
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Città #
Dallas 625
Southend 614
Menlo Park 523
Ashburn 366
Dublin 325
Fairfield 292
Chandler 193
Singapore 184
San Jose 167
Jacksonville 151
Santa Clara 147
Moscow 145
Woodbridge 129
Ann Arbor 124
Beijing 122
Wilmington 113
Seattle 109
Houston 106
Cambridge 93
Hong Kong 83
Milan 72
New York 66
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 34
Hanoi 31
Boardman 29
Johannesburg 29
Lauterbourg 27
Nanchang 25
San Mateo 22
Washington 21
Turku 17
Buffalo 16
Columbus 16
São Paulo 16
Shanghai 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
Chicago 7
Jinan 7
London 7
Ningbo 7
Poplar 7
Toronto 7
Abuja 6
Amsterdam 6
Brooklyn 6
Changsha 6
Haiphong 6
Manchester 6
North Bergen 6
Philadelphia 6
Rio de Janeiro 6
Roselle 6
San Francisco 6
Warsaw 6
Bengaluru 5
Denver 5
Dhaka 5
Falls Church 5
Jakarta 5
Lancaster 5
Naples 5
Norwalk 5
Redondo Beach 5
Stockholm 5
Sugar Grove 5
Aci Sant'Antonio 4
Belo Horizonte 4
Bishkek 4
Boston 4
Figino 4
Itri 4
Jiaxing 4
Totale 5.995
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Nome #
A case of 3243A>G mutation in mtDNA presenting as apparently idiopathic hyperCKemia. 420
A novel heteroplasmic tRNA(Ser(UCN)) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss 408
A new thymidine phosphorylase mutation causing elongation of the protein underlies mitochondrial neurogastrointestinal encephalomyopathy 382
A novel OPA1 mutation in a family with Autosomal Dominant Optic Atrophy 359
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients 355
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy. 339
Frequency of OPA1 and OPTN gene variations in 18 patients with normal tension glaucoma 318
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families 302
Sporadic myopathy, myoclonus, leukoencephalopathy, neurosensory deafness, hypertrophic cardiomyopathy and insulin resistance associated with the mitochondrial 8306 T>C MTTK mutation. 296
Oxidative stress-induced apoptosis in peripheral blood lymphocytes from patients with POLG-related disorders 294
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy. 286
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene. 275
Alu-Element Insertion In The Opa1 Intron Sequence Associated With ADOA 274
Mitochondria, oxidative stress and neurodegeneration. 274
Alu-element insertion in the OPA1 intron sequence associated with ADOA 265
Molecular genetic study of Leber’s hereditary optic neurophaty (LHON): mutation screening by sequencing of ND1, ND4, ND%, ND6 genes 262
Genetic leukoencephalopaties with unknown metabolic pathogenesis 257
Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy 244
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telithromycin consumption 239
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telythromicin consumption 230
Commentary to mitDNA research for the pathogenesis of mitochondrial disorders. 229
Heterogeneity of retinal manifestations in mitochondrial myopathy: genotype/phenotype correlation in our experience 225
Rapidly progressive neurodegeneration in a case with the 7472insC mutation and the A7472C polymorphism in the mtDNA tRNA ser(UCN) gene. 215
Leber hereditary optic neuropathy in 2 of 4 siblings with 11778 mtDNA mutation: clinical variability or effect of toxic exposure? 211
Sequence analysis of the complete mitochondrial genome in patients with mitochondrial encephaloneuromyopathies lacking the common pathogienic DNA mutations 183
null 178
Sporadic PEO caused by a novel POLG variation and a Twinkle mutation: digenic inheritance? 165
possible founder mutation as the cause of adoa in the province of Syracuse, Sicily 163
Erratum to: Redefining phenotypes associated with mitochondrial DNA single deletion 143
null 143
Mitochondrial recessive ataxia syndrome: A neurological rarity not to be missed. 132
null 111
Redefining phenotypes associated with mitochondrial DNA single deletion 93
null 89
Totale 8.359
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Categoria #
all - tutte 22.276
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 22.276
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022242 0 0 0 0 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
2026/2027418 88 62 170 86 12 0 0 0 0 0 0 0
Totale 8.359