IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

FASSONE, ELISA
 Distribuzione geografica
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Continente #
EU - Europa 1.587
NA - Nord America 1.056
AS - Asia 546
SA - Sud America 29
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 5
AF - Africa 4
Totale 3.237
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Nazione #
US - Stati Uniti d'America 1.007
GB - Regno Unito 509
DE - Germania 306
CN - Cina 267
IT - Italia 226
SE - Svezia 200
SG - Singapore 73
TR - Turchia 60
UA - Ucraina 59
FR - Francia 58
IN - India 52
CA - Canada 49
EU - Europa 46
IE - Irlanda 46
KR - Corea 43
FI - Finlandia 40
RU - Federazione Russa 35
NL - Olanda 28
HK - Hong Kong 21
PL - Polonia 21
CO - Colombia 20
BE - Belgio 17
ES - Italia 10
RO - Romania 10
UZ - Uzbekistan 10
AU - Australia 8
GR - Grecia 8
BR - Brasile 7
DK - Danimarca 6
ID - Indonesia 5
JP - Giappone 5
CH - Svizzera 3
JO - Giordania 3
EG - Egitto 2
IR - Iran 2
NZ - Nuova Zelanda 2
AL - Albania 1
AM - Armenia 1
BT - Bhutan 1
CI - Costa d'Avorio 1
CZ - Repubblica Ceca 1
EC - Ecuador 1
EE - Estonia 1
HR - Croazia 1
IM - Isola di Man 1
MA - Marocco 1
PK - Pakistan 1
TW - Taiwan 1
UY - Uruguay 1
VN - Vietnam 1
Totale 3.278
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Città #
Southend 452
Chandler 182
Beijing 67
Ann Arbor 65
Wilmington 65
Milan 64
Princeton 62
Mountain View 49
Dublin 43
Redmond 43
Seattle 43
Ashburn 38
Toronto 35
Singapore 33
Grafing 32
Somerville 32
Dearborn 30
Jacksonville 29
Phoenix 26
Fairfield 24
Sakarya 23
Nanjing 22
Des Moines 21
Serra 21
Boardman 20
Bogotá 20
New York 20
Warsaw 20
Andover 19
Bengaluru 19
Houston 19
Woodbridge 19
Frankfurt am Main 18
Hong Kong 16
Jinan 16
Hangzhou 15
Shanghai 15
Helsinki 14
Nanchang 14
Kiez 13
Medford 12
Redwood City 12
Brussels 11
Scranton 10
Tianjin 10
Eitensheim 9
Hamburg 9
Melzo 9
Guangzhou 8
Margão 8
Ottawa 8
Athens 7
Changsha 7
Zhengzhou 7
Bitonto 6
Hebei 6
Los Angeles 6
Petina 6
Turin 6
Auburn Hills 5
Jiaxing 5
Nürnberg 5
Rome 5
Shenyang 5
Berlin 4
Cagliari 4
Central 4
Delhi 4
Naples 4
Ningbo 4
Saint Petersburg 4
San Diego 4
Amman 3
Cuiabá 3
Cupertino 3
Fremont 3
Granada 3
Heidelberg 3
Kunming 3
Lanzhou 3
London 3
Mandi 3
Melbourne 3
Menlo Park 3
Norwalk 3
Rochester 3
Santhià 3
Sydney 3
Taiyuan 3
Zurich 3
A Coruña 2
Atlanta 2
Auckland 2
Borghetto di Vara 2
Bühl 2
Cairo 2
Changzhou 2
Deux-montagnes 2
Falls Church 2
Feltre 2
Totale 2.066
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Nome #
BIOCHEMICAL AND GENETIC APPROACHES TO UNRAVEL MITOCHONDRIAL COMPLEX I DEFICIENCY 354
The mitochondrial disulfide relay system protein GFER is mutated in autosomal recessive myopathy with congenital cataract and COX deficiency. 246
The mitochondrial disulfide relay system protein GFER is mutated in sutosomal-tecessive myopathy with vataract and vombined respiratory-chain deficiency 164
A novel MAPT mutation associated to late-onset spinal muscular atrophy without dementia in a large Italian family 164
Analisi molecolare del gene GAA e caratterizzazione di due nuove mutazioni di splicing in pazienti con deficit di maltasi acida. 161
Autosomal Recessive Ala93Thr mutation in caveolin-3 gene : a new family 160
Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study 156
Mitochondrial respiratory chain dysfunction in muscle from patients with Amyotrophic Lateral Sclerosis 143
Clinical features of an adult-onset Leigh syndrome caused by the T9176C mutation in the mitochondrial DNA ATPase 6 gene 141
A novel MAPT mutation associated to late-onset spinal muscular atrophy without dementia in a large Italian family 138
Aspetti clinici e molecolari in un paziente pediatrico affetto da Sindrome di Leigh associata alla mutazione mitocondriale m.14459G>A 136
Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia 132
mtDNA depletion in a case of fatal infant cytochrome c oxidase deficiency presenting with clinical feature of type 1 spinal muscular atrophy 126
Mitochondrial DNA G8363A mutation in the tRNA Lys gene : clinical features of a new family 118
Analisi di modelli cellulari in cui è compromessa l’attività di GFER, proteina chiave del Disulfide Relay System 117
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T > C mutation 114
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability 113
Clinical and genetical heterogeneity in a cohort of pediatric patients affected with mitochondrial disorders 105
The novel mitochondrial tRNAAsn gene mutation m.5709T>C produces ophthalmoparesis and respiratory impairment 93
Spasmi infantili e sindrome di Leigh: aspetti clinici concomitanti in una paziente pediatrica 92
The m.12316G>A mutation in the mitochondrial tRNA Leu(CUN) gene is associated with mitochondrial myopathy and respiratory impairment 92
CNS involvement in a cohort of pediatric patients affected with mitochondrial disorders caused by heterogeneous biochemical and genetic defects 91
Lower motor neuron disease with respiratory failure caused by a novel MAPT mutation 87
The mitochondrial disulfide relay system protein GFER is mutated in autosomal recessive myopathy with congenital cataract and COX deficiency 84
Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G>A mitochondrial DNA mutation 79
Una nuova mutazione nella subunità CO-II è associata a coma metabolico pediatrico con un grave deficit di Complesso IV 77
Totale 3.483
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Categoria #
all - tutte 8.157
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 8.157
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020308 54 9 7 2 8 33 22 17 66 57 17 16
2020/2021379 9 26 33 2 28 18 27 33 74 17 92 20
2021/2022361 18 19 10 32 16 34 38 12 57 23 41 61
2022/2023521 75 63 56 53 49 93 7 27 74 6 17 1
2023/2024296 3 27 16 26 90 16 21 21 2 17 28 29
2024/202521 21 0 0 0 0 0 0 0 0 0 0 0
Totale 3.483