IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

LUCCHINI, VALERIA
 Distribuzione geografica
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Continente #
EU - Europa 2.689
NA - Nord America 2.549
AS - Asia 2.300
Continente sconosciuto - Info sul continente non disponibili 357
SA - Sud America 182
AF - Africa 58
OC - Oceania 14
Totale 8.149
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Nazione #
US - Stati Uniti d'America 2.412
GB - Regno Unito 715
CN - Cina 711
SG - Singapore 583
IT - Italia 559
DE - Germania 403
SE - Svezia 283
BD - Bangladesh 219
VN - Vietnam 199
RU - Federazione Russa 162
HK - Hong Kong 150
IN - India 139
FR - Francia 124
UA - Ucraina 122
BR - Brasile 112
CA - Canada 112
TR - Turchia 92
NL - Olanda 85
FI - Finlandia 83
KR - Corea 69
IE - Irlanda 61
EU - Europa 57
JP - Giappone 36
CO - Colombia 33
CI - Costa d'Avorio 30
GR - Grecia 19
ID - Indonesia 19
BE - Belgio 16
AR - Argentina 12
UZ - Uzbekistan 12
IQ - Iraq 11
MX - Messico 11
AU - Australia 10
ES - Italia 9
PT - Portogallo 9
RO - Romania 8
CZ - Repubblica Ceca 7
MY - Malesia 7
PL - Polonia 7
SA - Arabia Saudita 7
CL - Cile 6
DK - Danimarca 6
NP - Nepal 6
PH - Filippine 6
PK - Pakistan 6
VE - Venezuela 6
ZA - Sudafrica 6
EC - Ecuador 4
JO - Giordania 4
KE - Kenya 4
KH - Cambogia 4
MA - Marocco 4
TW - Taiwan 4
BO - Bolivia 3
DZ - Algeria 3
EG - Egitto 3
KG - Kirghizistan 3
NZ - Nuova Zelanda 3
PE - Perù 3
TT - Trinidad e Tobago 3
AE - Emirati Arabi Uniti 2
AT - Austria 2
AZ - Azerbaigian 2
BH - Bahrain 2
CH - Svizzera 2
JM - Giamaica 2
MU - Mauritius 2
NG - Nigeria 2
PR - Porto Rico 2
PY - Paraguay 2
TH - Thailandia 2
BF - Burkina Faso 1
BN - Brunei Darussalam 1
BY - Bielorussia 1
CR - Costa Rica 1
CY - Cipro 1
DO - Repubblica Dominicana 1
FJ - Figi 1
GE - Georgia 1
GH - Ghana 1
GT - Guatemala 1
HN - Honduras 1
HR - Croazia 1
HT - Haiti 1
IL - Israele 1
JE - Jersey 1
KW - Kuwait 1
LC - Santa Lucia 1
LT - Lituania 1
LV - Lettonia 1
NO - Norvegia 1
PA - Panama 1
RS - Serbia 1
SN - Senegal 1
TZ - Tanzania 1
UY - Uruguay 1
Totale 7.849
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Città #
Southend 610
Singapore 353
Ashburn 260
Chandler 183
Beijing 159
Hong Kong 144
San Jose 118
Seattle 98
Princeton 92
Santa Clara 92
Ann Arbor 87
Wilmington 87
Milan 81
Jacksonville 76
Los Angeles 64
New York 64
Ho Chi Minh City 63
Dallas 62
Dublin 61
Redmond 59
Toronto 58
Woodbridge 58
Council Bluffs 57
Mountain View 55
Hanoi 52
Dearborn 51
Bengaluru 49
Fairfield 45
Nanjing 43
Boardman 40
Helsinki 38
Lauterbourg 37
Des Moines 36
Houston 35
Munich 35
Frankfurt am Main 33
Sakarya 32
Somerville 32
Buffalo 31
Rome 31
Abidjan 30
Athens 29
Bogotá 29
Serra 29
Andover 28
Ponte San Pietro 28
Ottawa 26
Moscow 24
Jinan 23
Nanchang 23
Shanghai 23
Redwood City 22
Guangzhou 21
Naples 20
Tokyo 20
Zhengzhou 20
Grafing 19
Phoenix 19
Cambridge 18
Changsha 17
Auburn Hills 16
Brussels 16
Hebei 15
Medford 15
Petina 15
Margão 14
Cangzhou 13
Da Nang 13
Columbus 12
Hangzhou 12
Shenyang 12
Tianjin 12
Bergamo 11
Boston 11
San Diego 11
Verona 11
Bitonto 10
Fuzhou 10
Eitensheim 9
Palermo 9
Turin 9
Turku 9
Hamburg 8
Hefei 8
Jiaxing 8
Montreal 8
Ningbo 8
The Dalles 8
Chengdu 7
Florence 7
Orem 7
Sunnyvale 7
Cagliari 6
Chicago 6
Genoa 6
Jakarta 6
Nürnberg 6
Pune 6
Quanzhou 6
San Francisco 6
Totale 4.518
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Nome #
Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1 392
IL DIFETTO OSSIDATIVO E LE ALTERAZIONI DEL DNA MITOCONDRIALE IN TOPI TRANSGENICI MODELLO ANIMALE DELLA ATASSIA SPINOCEREBELLARE DI TIPO 1 377
Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing 329
Mitochondrial changes in platelets are not related to those in skeletal muscle during human septic shock 282
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction 281
Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia 262
Clinical features of an adult-onset Leigh syndrome caused by the T9176C mutation in the mitochondrial DNA ATPase 6 gene 261
CNS involvement in a cohort of pediatric patients affected with mitochondrial disorders caused by heterogeneous biochemical and genetic defects 255
Mitochondrial respiratory chain dysfunction in muscle from patients with Amyotrophic Lateral Sclerosis 254
Familial amyotrophic lateral sclerosis with a novel Q23R mutation in the copper/zinc superoxide dismutase gene associated with muscle mitochondrial dysfunction 245
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up 242
mtDNA depletion in a case of fatal infant cytochrome c oxidase deficiency presenting with clinical feature of type 1 spinal muscular atrophy 240
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T > C mutation 235
Novel Q23R SOD1 mutation associated with muscle mitochondrial dysfunction 231
Miopatia progressiva con ptosi, oftalmoplagia e aspetti distrofici alla biopsia muscolare 219
Muscular Dystrophy : Central Nervous System {alpha}-Dystroglycan Glycosylation Defects and Brain Malformation 214
Follow-up of a large population of asymptomatic / oligosymptomatic hyperckemic subjects. 212
Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients 210
Severe acute multineuropathy in Churg-Strauss sindrome in a patient with a history of melanoma and asthma 208
Muscle mitochondrial oxidative defects in Amyotrophic Lateral Scelosis 207
Bank of DNA, cell lines and nerve-muscle-cardiac tissues 207
Congenital myopathy with ptosis, ophthalmoplegia and muscle dystrophic changes: a possible sporadic case of myosin heavy chain type IIa myopathy. 199
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy 193
Novel SOD1 Q23R mutation associated with muscle mitochondrial dysfunction in familial ALS International Meeting “Mutant SOD1 and familial ALS: from the molecule to man 192
Caratterizzazione clinica e molecolare della mutazione MERRF A8344G in una famiglia senza coinvolgimento del SNC 189
Incidental Mitochondrial Myopathy 181
Clinical and genetical heterogeneity in a cohort of pediatric patients affected with mitochondrial disorders 177
Miopatia mitocondriale con fenotipo clinico “limb-girdle”: studio morfologico e biomolecolare 176
A mouse model of facioscapulohumeral muscular dystrophy 175
Una nuova mutazione nella subunità CO-II è associata a coma metabolico pediatrico con un grave deficit di Complesso IV 175
Purkinje cell mitochondrial oxidative defect in the animal model of spinocerebellar ataxia type 1 Clinical and pathological aspects of an Italian patient with inclusion body myopathy and frontotemporal dementia carrying a novel mutation in valosin-containing protein gene. 174
COQ 10 deficiency in statin related Myopathy. 172
Statin related Myopathy and Co Q 10 deficiency 167
Nonconvulsive status epilepticus in a patient treated with carbamazepine 167
Muscle Coenzyme Q10 Level in Statin-Related Myopathy 157
Spasmi infantili e sindrome di Leigh: aspetti clinici concomitanti in una paziente pediatrica 157
Oxidative defect in a large cohort of genetically-determined SMA cases 126
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Totale 8.149
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Categoria #
all - tutte 19.687
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 19.687
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022475 34 12 8 58 18 25 50 17 74 38 55 86
2022/2023655 84 73 56 75 70 118 19 36 79 7 29 9
2023/2024392 12 23 29 22 117 31 19 22 10 21 36 50
2024/2025969 31 83 23 130 77 23 16 87 46 101 78 274
2025/20262.263 225 130 183 156 228 145 311 81 146 196 272 190
2026/2027121 121 0 0 0 0 0 0 0 0 0 0 0
Totale 8.149