IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

RIPOLONE, MICHELA
 Distribuzione geografica
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Continente #
NA - Nord America 1.984
AS - Asia 1.884
EU - Europa 1.762
SA - Sud America 171
AF - Africa 61
OC - Oceania 11
Totale 5.873
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Nazione #
US - Stati Uniti d'America 1.910
SG - Singapore 554
CN - Cina 553
IT - Italia 382
GB - Regno Unito 378
DE - Germania 259
HK - Hong Kong 185
SE - Svezia 152
BD - Bangladesh 144
FR - Francia 137
RU - Federazione Russa 135
BR - Brasile 127
VN - Vietnam 112
IN - India 94
NL - Olanda 62
TR - Turchia 56
KR - Corea 54
CA - Canada 53
FI - Finlandia 48
IE - Irlanda 48
UA - Ucraina 47
JP - Giappone 45
CI - Costa d'Avorio 31
ID - Indonesia 27
EU - Europa 23
PL - Polonia 23
BE - Belgio 14
CO - Colombia 14
DK - Danimarca 14
MX - Messico 14
AR - Argentina 13
GR - Grecia 11
AU - Australia 9
EG - Egitto 9
ES - Italia 9
CH - Svizzera 8
PH - Filippine 8
ZA - Sudafrica 8
IQ - Iraq 7
PK - Pakistan 7
AT - Austria 6
UZ - Uzbekistan 6
VE - Venezuela 6
EC - Ecuador 5
PT - Portogallo 5
SA - Arabia Saudita 5
AE - Emirati Arabi Uniti 4
CZ - Repubblica Ceca 4
BG - Bulgaria 3
DZ - Algeria 3
LT - Lituania 3
OM - Oman 3
PE - Perù 3
PY - Paraguay 3
SC - Seychelles 3
TW - Taiwan 3
AZ - Azerbaigian 2
CR - Costa Rica 2
EE - Estonia 2
HU - Ungheria 2
KG - Kirghizistan 2
LV - Lettonia 2
NO - Norvegia 2
NP - Nepal 2
NZ - Nuova Zelanda 2
RO - Romania 2
TH - Thailandia 2
TN - Tunisia 2
AM - Armenia 1
AO - Angola 1
BN - Brunei Darussalam 1
CU - Cuba 1
CY - Cipro 1
GA - Gabon 1
GE - Georgia 1
GT - Guatemala 1
HN - Honduras 1
HR - Croazia 1
IL - Israele 1
JM - Giamaica 1
JO - Giordania 1
KE - Kenya 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
MA - Marocco 1
ME - Montenegro 1
MY - Malesia 1
RS - Serbia 1
RW - Ruanda 1
SK - Slovacchia (Repubblica Slovacca) 1
TT - Trinidad e Tobago 1
Totale 5.896
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Città #
Singapore 337
Southend 312
Ashburn 249
Hong Kong 168
Chandler 148
Milan 114
Dallas 112
San Jose 111
Beijing 106
Seattle 66
Fairfield 63
Los Angeles 59
Ann Arbor 57
Santa Clara 55
Council Bluffs 54
Princeton 54
New York 51
Frankfurt am Main 48
Dublin 47
Wilmington 43
Boardman 39
Hanover 36
Ho Chi Minh City 35
Bengaluru 34
Buffalo 34
Hefei 34
Woodbridge 33
Abidjan 31
Houston 31
Hanoi 29
Lauterbourg 28
Shanghai 27
Guangzhou 26
Jacksonville 26
Moscow 26
Helsinki 25
Tokyo 25
Toronto 24
Des Moines 21
Jakarta 21
Mountain View 21
Nanjing 21
Rome 21
Athens 20
Cambridge 19
Munich 19
Redmond 19
Redwood City 18
Warsaw 18
Phoenix 17
The Dalles 17
Columbus 16
Dearborn 16
Kiez 16
Seoul 16
Somerville 16
São Paulo 15
Brussels 14
Jinan 13
Serra 13
Ottawa 12
Sakarya 12
Andover 11
Bogotá 11
Hangzhou 11
Ponte San Pietro 11
Hebei 10
Shenyang 10
Busto Arsizio 9
Eitensheim 9
Pisa 9
Turin 9
Cangzhou 8
Nuremberg 8
Atlanta 7
Berlin 7
Bologna 7
Chicago 7
Chongqing 7
Fuzhou 7
Istanbul 7
Nürnberg 7
Can Tho 6
Da Nang 6
Falls Church 6
Hamburg 6
Paris 6
San Francisco 6
Wuhan 6
Amsterdam 5
Brooklyn 5
Chennai 5
Genoa 5
Grafing 5
Ilhéus 5
Kunming 5
London 5
Medford 5
Mexico City 5
Minatomirai 5
Totale 3.477
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Nome #
Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1 383
Autophagy as a new therapeutic target in Duchenne muscular dystrophy 345
Drp1 overexpression induces desmin disassembling and drives kinesin-1 activation promoting mitochondrial trafficking in skeletal muscle 332
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of Andersen Disease associated with a new mutation in GBE1 gene 325
Reversal of Defective Mitochondrial Biogenesis in Limb-Girdle Muscular Dystrophy 2D by Independent Modulation of Histone and PGC-1α Acetylation 260
Skin-derived stem cells transplanted into resorable guides provide functional nerve regeneration after sciatic nerve resection 258
CNS involvement in a cohort of pediatric patients affected with mitochondrial disorders caused by heterogeneous biochemical and genetic defects 247
Early Findings in Neonatal Cases of RYR1-Related Congenital Myopathies 241
Low anaerobic threshold and increased skeletal muscle lactate production in subjects with Huntington's Disease 229
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions 206
Expanding the phenotypic spectrum of non-alcoholic fatty liver disease and hypertriglyceridemia 205
Elucidating the role of Agl in bladder carcinogenesis by generation and characterization of genetically engineered mice 202
cAMP-Epac2-mediated activation of Rap1 in developing male germ cells : RA-RhoGAP as a possible direct down-stream effector 200
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy 189
USP8, a regulator of endosomal sorting, is involved in mouse acrosome biogenesis through interaction with the spermatid ESCRT-0 complex and microtubules 187
Clinical and genetical heterogeneity in a cohort of pediatric patients affected with mitochondrial disorders 177
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy 177
Severe acute multineuropathy in Churg-Strauss syndrome in a patient with a history of melanoma 166
mUBPY, endocytic vesicle traffic and microtubule mediated transport in acrosome biogenesis. Comparative study between wild-type and Wobbler (L967Q Vps54) mice 163
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 157
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy 156
mUBPy in spermatogenic cells of Wobbler Mice 148
Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant 143
mUBPy and the Hrs-STAM complex in developing male germ cells 137
Age-progressive stratification of Becker muscular dystrophy patients: a focus on muscle biopsy fibrosis, inflammation and capillary network 132
Oxidative defect in a large cohort of genetically-determined SMA cases 126
Novel missense GARS gene mutation in an Italian family with hereditary distal motor neuropathy 122
The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy Controls 120
Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in Phospholamban Gene 98
MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization 95
Exploring multiorgan mitochondrial dysfunction in the switch toward progressive MASLD in AMLN mice 73
Artificial intelligence as a ploy to delve into the intricate link between genetics and mitochondria in patients with MASLD 63
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy 54
Skeletal muscle in spinal muscular atrophy: Critical insights from pathogenesis to therapeutic strategies 29
Expanding the genetic landscape of Dusty Core Disease: new RYR1 variants in Italian patients 13
A new MYH2 variant in an Italian patient expanding the clinical spectrum of MYH2-related myopathy 10
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Totale 6.177
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Categoria #
all - tutte 16.703
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 16.703
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202121 0 0 0 0 0 0 0 0 0 0 0 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
2025/20262.356 224 178 242 195 190 125 264 94 223 162 295 164
Totale 6.177