POGGESI, CORRADO
 Distribuzione geografica
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Continente #
NA - Nord America 15.899
EU - Europa 11.925
AS - Asia 6.316
SA - Sud America 783
Continente sconosciuto - Info sul continente non disponibili 294
AF - Africa 146
OC - Oceania 123
Totale 35.486
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Nazione #
US - Stati Uniti d'America 15.633
PL - Polonia 3.970
RU - Federazione Russa 2.751
IT - Italia 2.254
SG - Singapore 1.794
CN - Cina 1.443
HK - Hong Kong 977
VN - Vietnam 725
IE - Irlanda 641
BR - Brasile 619
SE - Svezia 556
KR - Corea 498
DE - Germania 380
FI - Finlandia 305
FR - Francia 287
UA - Ucraina 235
GB - Regno Unito 198
IN - India 175
CA - Canada 172
JO - Giordania 170
JP - Giappone 124
AU - Australia 116
BD - Bangladesh 112
CH - Svizzera 103
ID - Indonesia 94
AR - Argentina 56
BE - Belgio 53
ES - Italia 48
MX - Messico 44
NL - Olanda 42
IQ - Iraq 39
TR - Turchia 39
ZA - Sudafrica 37
CI - Costa d'Avorio 31
EC - Ecuador 29
CO - Colombia 21
PK - Pakistan 21
MA - Marocco 18
VE - Venezuela 17
GR - Grecia 16
LT - Lituania 15
PH - Filippine 15
CL - Cile 14
NG - Nigeria 13
AT - Austria 11
JM - Giamaica 11
UZ - Uzbekistan 11
KE - Kenya 10
PE - Perù 10
PY - Paraguay 9
SA - Arabia Saudita 9
DZ - Algeria 8
PT - Portogallo 8
TT - Trinidad e Tobago 8
TW - Taiwan 8
AL - Albania 7
EG - Egitto 7
KZ - Kazakistan 7
MY - Malesia 7
NZ - Nuova Zelanda 7
PR - Porto Rico 7
RO - Romania 7
SC - Seychelles 7
CR - Costa Rica 6
CZ - Repubblica Ceca 6
LU - Lussemburgo 6
RS - Serbia 6
TN - Tunisia 6
AZ - Azerbaigian 5
BO - Bolivia 5
IR - Iran 5
NP - Nepal 5
BJ - Benin 4
GT - Guatemala 4
LB - Libano 4
NO - Norvegia 4
SN - Senegal 4
AE - Emirati Arabi Uniti 3
BH - Bahrain 3
GE - Georgia 3
IL - Israele 3
MD - Moldavia 3
MN - Mongolia 3
SI - Slovenia 3
BB - Barbados 2
BG - Bulgaria 2
DK - Danimarca 2
DO - Repubblica Dominicana 2
EU - Europa 2
HN - Honduras 2
HU - Ungheria 2
KG - Kirghizistan 2
OM - Oman 2
PA - Panama 2
PS - Palestinian Territory 2
TH - Thailandia 2
UY - Uruguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AI - Anguilla 1
BN - Brunei Darussalam 1
Totale 35.179
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Città #
Warsaw 3.965
Santa Clara 2.722
Ashburn 1.881
Fairfield 1.396
Singapore 1.263
Hong Kong 823
Chandler 695
Woodbridge 636
Dublin 627
Seattle 600
Cambridge 564
Seoul 489
Houston 478
San Jose 464
Wilmington 449
Milan 430
Florence 359
Jacksonville 357
Beijing 343
Council Bluffs 325
Ann Arbor 320
Hefei 247
Buffalo 225
Ho Chi Minh City 202
Lawrence 192
Rome 191
Altamura 188
Los Angeles 184
Princeton 184
Lauterbourg 176
The Dalles 158
Munich 145
Boston 136
Hanoi 133
New York 124
Boardman 121
Dallas 113
Moscow 108
Helsinki 100
Bern 99
Mumbai 99
Tokyo 98
Dong Ket 96
San Diego 94
Melbourne 92
Medford 82
Jakarta 80
Shanghai 76
Kent 64
São Paulo 55
Turku 54
Brussels 52
Columbus 47
Norwalk 46
Redondo Beach 46
Naples 45
Bologna 44
Phoenix 44
Chicago 43
Frankfurt am Main 39
Turin 38
Clifton 36
Montreal 34
Guangzhou 32
London 32
Abidjan 31
Toronto 31
Orem 30
Paris 28
Figino 27
Da Nang 26
Dearborn 26
Falls Church 25
Palermo 25
Andover 23
Haiphong 22
Rio de Janeiro 22
Lappeenranta 21
Miano 21
Redwood City 21
Chennai 20
Falkenstein 20
Amsterdam 18
Barcelona 18
Hillsboro 18
Tianjin 18
Atlanta 17
Venice 17
Belo Horizonte 16
Brasília 16
Johannesburg 16
Poplar 16
Brooklyn 15
Siena 15
Baghdad 14
Biên Hòa 14
Catania 14
Mexico City 14
Perugia 14
Padua 13
Totale 24.382
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Nome #
Visco-elastic characteristics of the rat aorta 497
Novel insights on the relationship between T-tubular defects and contractile dysfunction in a mouse model of hypertrophic cardiomyopathy. 438
Atrial Remodeling in Hypertrophic Cardiomyopathy 409
Optogenetics design of mechanistically-based stimulation patterns for cardiac defibrillation. 379
The familial hypertrophic cardiomyopathy-associated myosin mutation R403Q accelerates tension generation and relaxation of human cardiac myofibrils 359
Pathogenesis of hypertrophic cardiomyopathy is mutation rather than disease specific: A comparison of the cardiac troponin T E163R and R92Q mouse models 353
Deleting exon 55 from the nebulin gene induces severe muscle weakness in a mouse model for nemaline myopathy 342
Isolation and Mechanical Measurements of Myofibrils from Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes. 331
Ablation of palladin in adult cardiac muscle causes cardiac dilation and systolic dysfunction 328
Altered Cross Bridge Kinetics in Skeletal Myofibrils from NEBDex55, a Novel Mouse Model of Nebulin-Based Nemaline Myopathy 328
Regulation of intracellular Na+ in health and disease: pathophysiological mechanisms and implications for treatment 327
Active and passive forces of isolated myofibrils from cardiac and fast skeletal muscle fibres of the frog. 321
Mutations in the central part of a Tropomyosin molecule alter Ca2+ sensitivity and tension relaxation of skeletal muscle myofibrils after troponin–tropomyosin removal and reconstitution 314
Deleting exon 55 from the nebulin gene induces severe muscle weakness in a mouse model for nemaline myopathy 311
Myocardial Dysfunction in Hypertrophic Cardiomyopathy: Primary Effects of Sarcomeric Mutations Versus Secondary EC-Coupling Remodelling 305
Susceptibility of isolated myofibrils to in vitro glutathionylation: potential relevance to muscle functions 305
Mechanical and Energetic Consequences of HCM-Causing Mutations 302
Late sodium current inhibitors to treat exercise induced obstruction in hypertrophic cardiomyopathy: an in vitro study in human myocardium. 300
C-Terminal Truncation of Troponin I and Substitutions of Non- Canonical Residues in the Central Part of Tropomyosin 1.1 Disrupt Thin Filament Switched Off State in Rabbit Psoas Myofibrils 299
Contractile effects of the exchange of cardiac troponin for fast skeletal troponin in rabbit psoas single myofibrils 285
Force regulation by Ca2+ in skinned single cardiac myocytes of frog. 283
Altered Ca2+ and Na+ homeostasis in human hypertrophic cardiomyopathy: Implications for arrhythmogenesis 283
Optical investigation of action potential and calcium handling maturation of hiPSC-cardiomyocytes on biomimetic substrates 283
The homozygous K280N troponin T mutation alters cross-bridge kinetics and energetics in human HCM 283
Effect of troponin Ca2+ binding properties on the kinetics of myofibril force initiation and relaxation 281
T-Tubular Electrical Defects Contribute to Blunted β-Adrenergic Response in Heart Failure. 280
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center 276
The Relaxation Properties of Myofibrils Are Compromised by Amino Acids that Stabilize α-Tropomyosin 266
A Novel Method of Isolating Myofibrils From Primary Cardiomyocyte Culture Suitable for Myofibril Mechanical Study 265
Quantitative assessment of passive electrical properties of the cardiac T-tubular system by FRAP microscopy 265
Mechanical measurements from single frog skeletal muscle myofibrils activated by rapid solution changes 264
Tropomyosin flexibility modulates Ca2+ sensitivity of thin filament and affects tension relaxation in skeletal muscle myofibrils after troponin-tropomyosin removal and reconstitution 258
Electrophysiological and Contractile Effects of Disopyramide in Patients With Obstructive Hypertrophic Cardiomyopathy: a Translational Study 249
Design of muscle contraction assist devices by liquid crystalline elastomers 248
Increased tension cost in human familial hypertrophic cardiomyopathy caused by the MYH7 mutation R403Q 247
Liquid Crystalline Networks toward Regenerative Medicine and Tissue Repair 246
The effects of phosphate on the contraction of single skeletal myofibrils 237
Development of Light-Responsive Liquid Crystalline Elastomers to Assist Cardiac Contraction 236
Action potential propagation in transverse-axial tubular system is impaired in heart failure 234
Real-time optical manipulation of cardiac conduction in intact hearts 231
Long-Term Prevalence of Systolic Dysfunction in MYBPC3 Versus MYH7-Related Hypertrophic Cardiomyopathy 230
Relaxation kinetics following sudden Ca(2+) reduction in single myofibrils from skeletal muscle 230
Absence of full-length dystrophin impairs normal maturation and contraction of cardiomyocytes derived from human induced pluripotent stem cells 229
Advanced Morpho-Functional Analysis on Ventricular and Atrial Tissue Reveals Cross-Bridge Kinetics Alterations and Sarcomere Energetic Impairment in Hcm Patients 228
Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: The impact of full-length dystrophin deficiency 216
The Missense E258K-MyBP-C Mutation Increases the Energy Cost of Tension Generation in Both Ventricular and Atrial Tissue from HCM Patients 216
The relation between sarcomere energetics and the rate of isometric tension relaxation in healthy and diseased cardiac muscle 213
The missense E258 K-MyBP-C mutation increases the energy cost of tension generation in both ventricular and atrial tissue from HCM patients 212
The harder the climb the better the view: The impact of substrate stiffness on cardiomyocyte fate 212
Myocardial overexpression of ANKRD1 causes sinus venosus defects and progressive diastolic dysfunction. 209
Ranolazine prevents phenotype development in a mouse model of hypertrophic cardiomyopathy 209
Chronic Atrial Fibrillation Alters the Functional Properties of Ifin the Human Atrium 206
Impact of Mavacamten on Force Generation in Single Myofibrils from Rabbit Psoas and Human Cardiac Muscle 205
Myosin isoform-dependent effect of omecamtiv mecarbil on the regulation of force generation in human cardiac muscle 204
ATPase and shortening rates in frog fast skeletal myofibrils by time-resolved measurements of protein-bound and free Pi. 202
Impact of detubulation on force and kinetics of cardiac muscle contraction 202
Advances in Stem Cell Modeling of Dystrophin-Associated Disease: Implications for the Wider World of Dilated Cardiomyopathy 202
New techniques in linear and non-linear laser optics in muscle research. 200
Impact of Genotype on the Occurrence of Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy. 200
The transverse-axial tubular system of cardiomyocytes. 196
Slower Calcium Handling Balances Faster Cross-Bridge Cycling in Human MYBPC3 HCM 195
[Molecular targets and novel pharmacological options to prevent myocardial hypertrophic remodeling] 195
Late Sodium Current Inhibition Reverses Electro-Mechanical Dysfunction in Human Hypertrophic Cardiomyopathy 193
BPS2025 - Long-term effect of Mavacamten impact force and sarcomere density in a MYBPC3 iPSC-cardiomyocyte model of hypertrophic cardiomyopathy 192
Contemporary Insights Into the Genetics of Hypertrophic Cardiomyopathy: Toward a New Era in Clinical Testing? 192
A force transducer and a length-ramp generator for mechanical investigations of frog-heart myocytes. 191
Impaired diastolic function after exchange of endogenous troponin I with C-terminal truncated troponin I in human cardiac muscle 189
Whole heart cytoarchitecture at micron-scale resolution 189
Extraction and Replacement of the Tropomyosin-Troponin Complex in Isolated Myofibrils. 189
Optogenetic manipulation of cardiac electrical dynamics using sub-threshold illumination: dissecting the role of cardiac alternans in terminating rapid rhythms 188
Tension generation and relaxation in single myofibrils from human atrial and ventricular myocardium. 187
Design of Biocompatible Liquid Cristal Elastomers Reproducing the Mechanical Properties of Human Cardiac Muscle 187
R4496C RyR2 mutation impairs atrial and ventricular contractility 186
Il flip teaching nel Corso d Laurea in Medicina e Chirurgia dell’Università di Firenze a supporto dell’applicazione della direttiva europea 2013/55/UE 183
Myocardial overexpression of ANKRD1 affects developmental cardiac remodeling and leads to adult diastolic dysfunction 182
Time resolved depression of isometric force by Mavacamten in single myofibrils from rabbit psoas and human cardiac muscle 181
Impact of tropomyosin isoform composition on fast skeletal muscle thin filament regulation and force development 179
Faster cross-bridge relaxation rates correlate with increased tension cost in HCM with the R403Q Myh7 Mutation 178
Calcium binding kinetics of troponin C strongly modulate cooperative activation and tension kinetics in cardiac muscle 178
Characterization of the cross-bridge force-generating step using inorganic phosphate and BDM in myofibrils from rabbit skeletal muscles 178
The HCM-associated cardiac Troponin T mutation K280N accelerates tension generation and relaxation in human cardiac myofibrils 178
Microled Illumination Towards Liquid Crystalline Elastomers Based Cardiac Contraction Assistance 176
Optogenetic confirmation of transverse‐tubular membrane excitability in intact cardiac myocytes 175
Reply to entcheva: The impact of T-tubules on action potential propagation in cardiac tissue 175
Efficacy of Ranolazine in Patients With Symptomatic Hypertrophic Cardiomyopathy: The RESTYLE-HCM Randomized, Double-Blind, Placebo-Controlled Study 174
Mavacamten depresses human atrial contractility in the same EC50% range as human ventricle 173
Defects in T-tubular electrical activity underlie local alterations of calcium release in heart failure 173
Myofilament calcium sensitivity does not affect cross-bridge activation-relaxation kinetics 171
HDAC6 contributes to pathological responses of heart and skeletal muscle to chronic angiotensin-II signaling. 171
Mutations in MYH7 reduce the force generating capacity of sarcomeres in human familial hypertrophic cardiomyopathy. 170
No direct effect of creatine phosphate on the cross-bridge cycle in cardiac myofibrils 170
Paradoxical prolongation of QT interval during exercise in patients with hypertrophic cardiomyopathy: cellular mechanisms and implications for diastolic function 169
The HCM-associated cardiac Troponin T mutation K280N increases the energetic cost of tension generation in human cardiac myofibrils 169
Faster cross-bridge detachment and increased tension cost in human hypertrophic cardiomyopathy with the R403Q MYH7 mutation 169
Is fast cross-bridge detachment a common feature to MYH7 and MYBP3 FHC-associated mutations in human cardiac myofibrils? 168
Functional imaging of skeletal muscle fiber in different physiological states by Second Harmonic Generation 167
Photoresponsive Polymer-Based Biomimetic Contractile Units as Building Block for Artificial Muscles 166
Genotype-Driven Pathogenesis of Atrial Fibrillation in Hypertrophic Cardiomyopathy: The Case of Different TNNT2 Mutations 166
MOLECULES INVOLVED IN CA2+ REMOVAL FROM THE MYOPLASM 165
Functional impact of TnT mutations responsible for Hypertrophic Cardiomyopathy on Tn-exchanged single myofibrils 165
Totale 23.411
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Categoria #
all - tutte 92.157
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 92.157
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.343 0 109 135 49 94 49 71 93 64 73 268 338
2022/20233.201 320 519 150 236 245 548 339 172 453 19 74 126
2023/20241.161 57 143 193 73 83 104 60 258 21 44 65 60
2024/20258.212 293 891 473 1.136 2.373 1.014 161 560 369 201 316 425
2025/202610.573 1.010 1.255 781 769 1.129 445 1.149 496 718 665 696 1.460
2026/2027591 349 242 0 0 0 0 0 0 0 0 0 0
Totale 35.486