IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

LUCCHINI, VALERIA
 Distribuzione geografica
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Continente #
NA - Nord America 2.862
EU - Europa 2.717
AS - Asia 2.353
Continente sconosciuto - Info sul continente non disponibili 357
SA - Sud America 187
AF - Africa 59
OC - Oceania 15
Totale 8.550
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Nazione #
US - Stati Uniti d'America 2.705
GB - Regno Unito 721
CN - Cina 713
SG - Singapore 587
IT - Italia 578
DE - Germania 403
SE - Svezia 283
BD - Bangladesh 252
VN - Vietnam 203
RU - Federazione Russa 162
HK - Hong Kong 153
IN - India 141
FR - Francia 124
UA - Ucraina 122
CA - Canada 119
BR - Brasile 117
TR - Turchia 93
NL - Olanda 86
FI - Finlandia 83
KR - Corea 69
IE - Irlanda 61
EU - Europa 57
JP - Giappone 37
CO - Colombia 33
CI - Costa d'Avorio 30
ID - Indonesia 20
GR - Grecia 19
BE - Belgio 16
MX - Messico 13
AR - Argentina 12
UZ - Uzbekistan 12
AU - Australia 11
IQ - Iraq 11
ES - Italia 9
PT - Portogallo 9
PL - Polonia 8
RO - Romania 8
SA - Arabia Saudita 8
CZ - Repubblica Ceca 7
MY - Malesia 7
PH - Filippine 7
CL - Cile 6
DK - Danimarca 6
NP - Nepal 6
PK - Pakistan 6
TT - Trinidad e Tobago 6
VE - Venezuela 6
ZA - Sudafrica 6
JM - Giamaica 5
KE - Kenya 5
CR - Costa Rica 4
EC - Ecuador 4
JO - Giordania 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
AE - Emirati Arabi Uniti 2
AT - Austria 2
AZ - Azerbaigian 2
BH - Bahrain 2
CH - Svizzera 2
MU - Mauritius 2
NG - Nigeria 2
PR - Porto Rico 2
PY - Paraguay 2
TH - Thailandia 2
AL - Albania 1
BF - Burkina Faso 1
BN - Brunei Darussalam 1
BY - Bielorussia 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
SV - El Salvador 1
TZ - Tanzania 1
UY - Uruguay 1
VG - Isole Vergini Britanniche 1
Totale 8.250
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Città #
Southend 610
Singapore 356
Ashburn 348
Chandler 183
Beijing 159
Hong Kong 145
San Jose 130
Santa Clara 105
Seattle 99
Princeton 92
Council Bluffs 91
Wilmington 89
Ann Arbor 87
Milan 85
Jacksonville 79
Los Angeles 69
New York 68
Dallas 64
Ho Chi Minh City 63
Toronto 63
Dublin 61
Redmond 59
Woodbridge 58
Mountain View 55
Hanoi 54
Dearborn 51
Bengaluru 49
Fairfield 45
Nanjing 43
Boardman 40
Helsinki 38
Des Moines 37
Lauterbourg 37
Houston 35
Munich 35
Rome 35
Frankfurt am Main 33
Sakarya 32
Somerville 32
Buffalo 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
Tokyo 21
Naples 20
Phoenix 20
Zhengzhou 20
Grafing 19
Cambridge 18
Changsha 17
Auburn Hills 16
Brussels 16
Hebei 15
Medford 15
Petina 15
Da Nang 14
Margão 14
Cangzhou 13
Columbus 12
Hangzhou 12
Shenyang 12
Tianjin 12
Bergamo 11
Boston 11
San Diego 11
Verona 11
Bitonto 10
Chicago 10
Fuzhou 10
Eitensheim 9
Palermo 9
Turin 9
Turku 9
Florence 8
Hamburg 8
Hefei 8
Jiaxing 8
Montreal 8
Ningbo 8
Philadelphia 8
São Paulo 8
The Dalles 8
Washington 8
Cagliari 7
Chengdu 7
Orem 7
Sunnyvale 7
Atlanta 6
Genoa 6
Jakarta 6
Totale 4.717
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Nome #
Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1 407
IL DIFETTO OSSIDATIVO E LE ALTERAZIONI DEL DNA MITOCONDRIALE IN TOPI TRANSGENICI MODELLO ANIMALE DELLA ATASSIA SPINOCEREBELLARE DI TIPO 1 403
Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing 345
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction 299
Mitochondrial changes in platelets are not related to those in skeletal muscle during human septic shock 290
Clinical features of an adult-onset Leigh syndrome caused by the T9176C mutation in the mitochondrial DNA ATPase 6 gene 277
CNS involvement in a cohort of pediatric patients affected with mitochondrial disorders caused by heterogeneous biochemical and genetic defects 277
Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia 276
Mitochondrial respiratory chain dysfunction in muscle from patients with Amyotrophic Lateral Sclerosis 268
Familial amyotrophic lateral sclerosis with a novel Q23R mutation in the copper/zinc superoxide dismutase gene associated with muscle mitochondrial dysfunction 261
mtDNA depletion in a case of fatal infant cytochrome c oxidase deficiency presenting with clinical feature of type 1 spinal muscular atrophy 261
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up 253
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T > C mutation 243
Novel Q23R SOD1 mutation associated with muscle mitochondrial dysfunction 240
Muscular Dystrophy : Central Nervous System {alpha}-Dystroglycan Glycosylation Defects and Brain Malformation 229
Follow-up of a large population of asymptomatic / oligosymptomatic hyperckemic subjects. 223
Miopatia progressiva con ptosi, oftalmoplagia e aspetti distrofici alla biopsia muscolare 221
Muscle mitochondrial oxidative defects in Amyotrophic Lateral Scelosis 216
Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients 215
Severe acute multineuropathy in Churg-Strauss sindrome in a patient with a history of melanoma and asthma 213
Bank of DNA, cell lines and nerve-muscle-cardiac tissues 212
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy 211
Congenital myopathy with ptosis, ophthalmoplegia and muscle dystrophic changes: a possible sporadic case of myosin heavy chain type IIa myopathy. 204
Novel SOD1 Q23R mutation associated with muscle mitochondrial dysfunction in familial ALS International Meeting “Mutant SOD1 and familial ALS: from the molecule to man 202
Clinical and genetical heterogeneity in a cohort of pediatric patients affected with mitochondrial disorders 199
Caratterizzazione clinica e molecolare della mutazione MERRF A8344G in una famiglia senza coinvolgimento del SNC 195
Una nuova mutazione nella subunità CO-II è associata a coma metabolico pediatrico con un grave deficit di Complesso IV 188
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. 185
A mouse model of facioscapulohumeral muscular dystrophy 183
Incidental Mitochondrial Myopathy 183
Miopatia mitocondriale con fenotipo clinico “limb-girdle”: studio morfologico e biomolecolare 178
Statin related Myopathy and Co Q 10 deficiency 174
COQ 10 deficiency in statin related Myopathy. 174
Nonconvulsive status epilepticus in a patient treated with carbamazepine 171
Muscle Coenzyme Q10 Level in Statin-Related Myopathy 169
Spasmi infantili e sindrome di Leigh: aspetti clinici concomitanti in una paziente pediatrica 167
Oxidative defect in a large cohort of genetically-determined SMA cases 129
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Totale 8.550
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Categoria #
all - tutte 20.773
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 20.773
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022421 0 0 0 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
2026/2027522 121 170 158 73 0 0 0 0 0 0 0 0
Totale 8.550