RIPOLONE, MICHELA
 Distribuzione geografica
Continente #
NA - Nord America 2.328
AS - Asia 1.966
EU - Europa 1.832
Continente sconosciuto - Info sul continente non disponibili 307
SA - Sud America 176
AF - Africa 61
OC - Oceania 11
Totale 6.681
Nazione #
US - Stati Uniti d'America 2.221
SG - Singapore 563
CN - Cina 556
IT - Italia 448
GB - Regno Unito 378
DE - Germania 260
BD - Bangladesh 199
HK - Hong Kong 187
SE - Svezia 153
FR - Francia 137
RU - Federazione Russa 136
BR - Brasile 130
VN - Vietnam 122
IN - India 94
CA - Canada 73
NL - Olanda 63
TR - Turchia 57
KR - Corea 54
FI - Finlandia 48
IE - Irlanda 48
UA - Ucraina 47
JP - Giappone 46
CI - Costa d'Avorio 31
ID - Indonesia 28
EU - Europa 23
PL - Polonia 23
CO - Colombia 15
MX - Messico 15
BE - Belgio 14
DK - Danimarca 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
VE - Venezuela 7
AT - Austria 6
UZ - Uzbekistan 6
CR - Costa Rica 5
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
GT - Guatemala 3
JM - Giamaica 3
LT - Lituania 3
OM - Oman 3
PE - Perù 3
PY - Paraguay 3
SC - Seychelles 3
TW - Taiwan 3
AZ - Azerbaigian 2
EE - Estonia 2
HN - Honduras 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
TT - Trinidad e Tobago 2
AM - Armenia 1
AO - Angola 1
BN - Brunei Darussalam 1
CU - Cuba 1
CY - Cipro 1
GA - Gabon 1
GE - Georgia 1
GP - Guadalupe 1
HR - Croazia 1
IL - Israele 1
JO - Giordania 1
KE - Kenya 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
LC - Santa Lucia 1
MA - Marocco 1
ME - Montenegro 1
MY - Malesia 1
RS - Serbia 1
RW - Ruanda 1
SK - Slovacchia (Repubblica Slovacca) 1
SV - El Salvador 1
Totale 6.397
Città #
Singapore 340
Southend 312
Ashburn 275
Hong Kong 168
Chandler 148
San Jose 129
Milan 127
Dallas 116
Beijing 107
Santa Clara 101
Council Bluffs 79
Los Angeles 69
Seattle 68
Fairfield 63
Ann Arbor 57
Princeton 54
New York 53
Frankfurt am Main 48
Dublin 47
Wilmington 45
Boardman 40
Buffalo 40
Ho Chi Minh City 38
Hanover 36
Jacksonville 36
Hanoi 35
Bengaluru 34
Hefei 34
Houston 33
Woodbridge 33
Abidjan 31
Lauterbourg 28
Shanghai 27
Guangzhou 26
Moscow 26
Helsinki 25
Tokyo 25
Toronto 25
Rome 23
Des Moines 21
Jakarta 21
Mountain View 21
Nanjing 21
Phoenix 21
Athens 20
Cambridge 19
Munich 19
Redmond 19
Redwood City 19
The Dalles 18
Warsaw 18
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
Atlanta 8
Bologna 8
Cangzhou 8
Chicago 8
Nuremberg 8
Bari 7
Berlin 7
Brooklyn 7
Chongqing 7
Fuzhou 7
Istanbul 7
London 7
Montreal 7
Nürnberg 7
Can Tho 6
Da Nang 6
Falls Church 6
Figino 6
Hamburg 6
Mexico City 6
Naples 6
Paris 6
San Francisco 6
Washington 6
Wuhan 6
Amsterdam 5
Chennai 5
Genoa 5
Totale 3.681
Nome #
Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1 397
Drp1 overexpression induces desmin disassembling and drives kinesin-1 activation promoting mitochondrial trafficking in skeletal muscle 356
Autophagy as a new therapeutic target in Duchenne muscular dystrophy 355
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of Andersen Disease associated with a new mutation in GBE1 gene 343
Reversal of Defective Mitochondrial Biogenesis in Limb-Girdle Muscular Dystrophy 2D by Independent Modulation of Histone and PGC-1α Acetylation 272
Skin-derived stem cells transplanted into resorable guides provide functional nerve regeneration after sciatic nerve resection 270
CNS involvement in a cohort of pediatric patients affected with mitochondrial disorders caused by heterogeneous biochemical and genetic defects 266
Early Findings in Neonatal Cases of RYR1-Related Congenital Myopathies 254
Low anaerobic threshold and increased skeletal muscle lactate production in subjects with Huntington's Disease 238
Expanding the phenotypic spectrum of non-alcoholic fatty liver disease and hypertriglyceridemia 221
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions 215
Elucidating the role of Agl in bladder carcinogenesis by generation and characterization of genetically engineered mice 209
cAMP-Epac2-mediated activation of Rap1 in developing male germ cells : RA-RhoGAP as a possible direct down-stream effector 208
USP8, a regulator of endosomal sorting, is involved in mouse acrosome biogenesis through interaction with the spermatid ESCRT-0 complex and microtubules 205
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy 199
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy 192
Clinical and genetical heterogeneity in a cohort of pediatric patients affected with mitochondrial disorders 180
Severe acute multineuropathy in Churg-Strauss syndrome in a patient with a history of melanoma 176
mUBPY, endocytic vesicle traffic and microtubule mediated transport in acrosome biogenesis. Comparative study between wild-type and Wobbler (L967Q Vps54) mice 169
MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization 166
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy 164
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 160
Age-progressive stratification of Becker muscular dystrophy patients: a focus on muscle biopsy fibrosis, inflammation and capillary network 157
Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant 156
mUBPy in spermatogenic cells of Wobbler Mice 152
mUBPy and the Hrs-STAM complex in developing male germ cells 140
The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy Controls 129
Oxidative defect in a large cohort of genetically-determined SMA cases 128
Novel missense GARS gene mutation in an Italian family with hereditary distal motor neuropathy 126
Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in Phospholamban Gene 107
Exploring multiorgan mitochondrial dysfunction in the switch toward progressive MASLD in AMLN mice 93
Artificial intelligence as a ploy to delve into the intricate link between genetics and mitochondria in patients with MASLD 84
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy 61
Skeletal muscle in spinal muscular atrophy: Critical insights from pathogenesis to therapeutic strategies 55
A new MYH2 variant in an Italian patient expanding the clinical spectrum of MYH2-related myopathy 27
Expanding the genetic landscape of Dusty Core Disease: new RYR1 variants in Italian patients 23
Glycogenin-1 deficiency: a case report and review of the literature 19
null 6
null 3
Totale 6.681
Categoria #
all - tutte 18.165
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 18.165


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022342 0 0 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
2025/20262.422 224 178 242 195 190 125 264 94 223 162 295 230
2026/2027438 201 196 41 0 0 0 0 0 0 0 0 0
Totale 6.681