DA POZZO, PAOLA
 Distribuzione geografica
Continente #
NA - Nord America 51
EU - Europa 27
AS - Asia 12
OC - Oceania 9
AF - Africa 2
Totale 101
Nazione #
US - Stati Uniti d'America 50
IT - Italia 19
AU - Australia 9
JP - Giappone 7
GB - Regno Unito 4
SG - Singapore 4
GH - Ghana 2
NL - Olanda 2
ES - Italia 1
IL - Israele 1
MQ - Martinica 1
RU - Federazione Russa 1
Totale 101
Città #
Siena 10
New Brunswick 8
Tokyo 5
Chicago 4
Denver 4
Madison 4
Omaha 4
Seattle 4
Ashburn 3
Melbourne 3
Perth 3
Sydney 3
Accra 2
Amsterdam 2
Boardman 2
Cernusco sul Naviglio 2
Los Angeles 2
Padova 2
Piermont 2
Rome 2
Stockport 2
Barcelona 1
Buffalo 1
Cleveland 1
Dallas 1
Fort-de-France 1
Herndon 1
Karasawa 1
Manchester 1
Narita 1
New York 1
Norfolk 1
Oxford 1
Providence 1
Rehovot 1
Rochester 1
Rockville 1
Totale 89
Nome #
Redefining phenotypes associated with mitochondrial DNA single deletion, file e0feeaa5-a14b-44d2-e053-6605fe0a8db0 35
Sporadic PEO caused by a novel POLG variation and a Twinkle mutation: digenic inheritance?, file e0feeaa6-6d62-44d2-e053-6605fe0a8db0 25
Mitochondrial recessive ataxia syndrome: A neurological rarity not to be missed., file e0feeaa6-738f-44d2-e053-6605fe0a8db0 17
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telithromycin consumption [3], file e0feeaa6-037a-44d2-e053-6605fe0a8db0 10
Oxidative stress-induced apoptosis in peripheral blood lymphocytes from patients with POLG-related disorders, file e0feeaa6-2eb9-44d2-e053-6605fe0a8db0 4
Erratum to: Redefining phenotypes associated with mitochondrial DNA single deletion, file e0feeaa6-7167-44d2-e053-6605fe0a8db0 4
null, file e0feeaa4-bdc8-44d2-e053-6605fe0a8db0 2
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy., file e0feeaa4-c207-44d2-e053-6605fe0a8db0 1
Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy., file e0feeaa4-ea59-44d2-e053-6605fe0a8db0 1
Mitochondria, oxidative stress and neurodegeneration., file e0feeaa5-a306-44d2-e053-6605fe0a8db0 1
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients, file e0feeaaa-6321-44d2-e053-6605fe0a8db0 1
Totale 101
Categoria #
all - tutte 1.187
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 1.187


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211 0 0 0 0 0 0 1 0 0 0 0 0
2021/20221 0 0 0 0 0 0 0 0 0 0 1 0
2022/202391 5 12 8 2 18 8 1 14 14 8 1 0
Totale 101