IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

RIPOLONE, MICHELA
 Distribuzione geografica
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Continente #
EU - Europa 1.532
NA - Nord America 1.499
AS - Asia 1.235
SA - Sud America 132
AF - Africa 47
OC - Oceania 11
Totale 4.456
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Nazione #
US - Stati Uniti d'America 1.458
CN - Cina 478
GB - Regno Unito 368
SG - Singapore 335
IT - Italia 271
DE - Germania 256
SE - Svezia 150
HK - Hong Kong 119
FR - Francia 103
BR - Brasile 101
RU - Federazione Russa 95
IN - India 84
NL - Olanda 59
TR - Turchia 54
KR - Corea 50
IE - Irlanda 47
UA - Ucraina 46
FI - Finlandia 39
CA - Canada 35
JP - Giappone 33
CI - Costa d'Avorio 31
EU - Europa 23
ID - Indonesia 22
PL - Polonia 21
VN - Vietnam 16
BE - Belgio 14
DK - Danimarca 12
CO - Colombia 11
GR - Grecia 10
AU - Australia 9
CH - Svizzera 8
AR - Argentina 7
AT - Austria 6
EG - Egitto 5
PT - Portogallo 5
UZ - Uzbekistan 5
CZ - Repubblica Ceca 4
EC - Ecuador 4
ES - Italia 4
IQ - Iraq 4
MX - Messico 4
SA - Arabia Saudita 4
AE - Emirati Arabi Uniti 3
BD - Bangladesh 3
BG - Bulgaria 3
OM - Oman 3
PE - Perù 3
PH - Filippine 3
PK - Pakistan 3
PY - Paraguay 3
SC - Seychelles 3
TW - Taiwan 3
VE - Venezuela 3
AZ - Azerbaigian 2
DZ - Algeria 2
EE - Estonia 2
LT - Lituania 2
NP - Nepal 2
NZ - Nuova Zelanda 2
RO - Romania 2
ZA - Sudafrica 2
AM - Armenia 1
AO - Angola 1
BN - Brunei Darussalam 1
CU - Cuba 1
GA - Gabon 1
GE - Georgia 1
HU - Ungheria 1
IL - Israele 1
JM - Giamaica 1
JO - Giordania 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LV - Lettonia 1
MA - Marocco 1
ME - Montenegro 1
MY - Malesia 1
NO - Norvegia 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
TN - Tunisia 1
Totale 4.479
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Città #
Southend 312
Singapore 205
Ashburn 191
Chandler 148
Hong Kong 115
Dallas 107
Beijing 101
Milan 99
Seattle 66
Fairfield 63
Ann Arbor 57
Princeton 54
Dublin 46
Frankfurt am Main 46
Wilmington 42
Council Bluffs 41
Hanover 36
Santa Clara 35
Bengaluru 34
Hefei 34
Woodbridge 33
Abidjan 31
Los Angeles 31
Houston 30
Jacksonville 25
Guangzhou 24
Boardman 23
Shanghai 23
Buffalo 21
Des Moines 21
Mountain View 21
Toronto 21
Jakarta 20
Nanjing 20
Athens 19
Cambridge 19
Helsinki 19
Munich 19
New York 19
Redmond 19
Redwood City 18
Columbus 16
Dearborn 16
Kiez 16
Somerville 16
Tokyo 16
Warsaw 16
Brussels 14
Phoenix 14
Jinan 13
Moscow 13
Serra 13
The Dalles 13
Sakarya 12
Seoul 12
São Paulo 12
Andover 11
Bogotá 11
Hangzhou 11
Ponte San Pietro 11
Hebei 10
Shenyang 10
Busto Arsizio 9
Eitensheim 9
Ottawa 9
Pisa 9
Rome 9
Cangzhou 8
Nuremberg 8
Fuzhou 7
Istanbul 7
Nürnberg 7
Berlin 6
Falls Church 6
Hamburg 6
Turin 6
Wuhan 6
Chicago 5
Grafing 5
Kunming 5
Medford 5
Minatomirai 5
Nanchang 5
San Diego 5
San Francisco 5
Taizhou 5
Bitonto 4
Brooklyn 4
Cagliari 4
Campinas 4
Changsha 4
Delhi 4
Dong Ket 4
Fremont 4
Genoa 4
Limbiate 4
Margão 4
Melbourne 4
Paris 4
Quanzhou 4
Totale 2.797
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Nome #
Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1 319
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of Andersen Disease associated with a new mutation in GBE1 gene 297
Autophagy as a new therapeutic target in Duchenne muscular dystrophy 295
Drp1 overexpression induces desmin disassembling and drives kinesin-1 activation promoting mitochondrial trafficking in skeletal muscle 265
Reversal of Defective Mitochondrial Biogenesis in Limb-Girdle Muscular Dystrophy 2D by Independent Modulation of Histone and PGC-1α Acetylation 226
Skin-derived stem cells transplanted into resorable guides provide functional nerve regeneration after sciatic nerve resection 204
Early Findings in Neonatal Cases of RYR1-Related Congenital Myopathies 196
Low anaerobic threshold and increased skeletal muscle lactate production in subjects with Huntington's Disease 178
Expanding the phenotypic spectrum of non-alcoholic fatty liver disease and hypertriglyceridemia 174
cAMP-Epac2-mediated activation of Rap1 in developing male germ cells : RA-RhoGAP as a possible direct down-stream effector 166
CNS involvement in a cohort of pediatric patients affected with mitochondrial disorders caused by heterogeneous biochemical and genetic defects 159
Clinical and genetical heterogeneity in a cohort of pediatric patients affected with mitochondrial disorders 152
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions 149
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy 146
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy 146
Elucidating the role of Agl in bladder carcinogenesis by generation and characterization of genetically engineered mice 145
mUBPY, endocytic vesicle traffic and microtubule mediated transport in acrosome biogenesis. Comparative study between wild-type and Wobbler (L967Q Vps54) mice 140
USP8, a regulator of endosomal sorting, is involved in mouse acrosome biogenesis through interaction with the spermatid ESCRT-0 complex and microtubules 140
Neuropathological study of skeletal muscle, heart, liver, and brainin a neonatal form of glycogen storage disease type IV associated with a newmutation in GBE1 gene 138
mUBPy in spermatogenic cells of Wobbler Mice 128
Severe acute multineuropathy in Churg-Strauss syndrome in a patient with a history of melanoma 120
mUBPy and the Hrs-STAM complex in developing male germ cells 119
Novel missense GARS gene mutation in an Italian family with hereditary distal motor neuropathy 114
Oxidative defect in a large cohort of genetically-determined SMA cases 107
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy 104
Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant 94
The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy Controls 77
Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in Phospholamban Gene 69
Age-progressive stratification of Becker muscular dystrophy patients: a focus on muscle biopsy fibrosis, inflammation and capillary network 65
MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization 65
null 6
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy 3
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Totale 4.709
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Categoria #
all - tutte 13.717
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 13.717
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021241 0 0 0 0 20 32 20 33 38 22 55 21
2021/2022404 41 21 21 22 20 31 42 13 47 41 29 76
2022/2023495 62 57 41 57 48 75 16 36 56 8 25 14
2023/2024337 12 26 27 21 79 29 11 16 10 20 46 40
2024/2025881 35 69 26 94 68 38 49 82 52 81 104 183
2025/2026888 224 178 242 195 49 0 0 0 0 0 0 0
Totale 4.709