statistiche ricercatore

statistiche per MEOLA, GIOVANNI

Distribuzione geografica
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Continente #
NA - Nord America 4242
EU - Europa 2728
AS - Asia 1186
OC - Oceania 105
SA - Sud America 98
AF - Africa 54
Continente sconosciuto - Info sul continente non disponibili 7
Totale 8420
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Nazione #
US - Stati Uniti d'America 3997
DE - Germania 833
IT - Italia 525
CN - Cina 436
GB - Regno Unito 319
FR - Francia 242
CA - Canada 216
KR - Corea 177
NL - Olanda 156
JP - Giappone 155
IN - India 124
RU - Federazione Russa 90
AU - Australia 88
UA - Ucraina 77
ID - Indonesia 73
ES - Italia 62
BR - Brasile 53
CZ - Repubblica Ceca 51
EU - Europa 49
CH - Svizzera 39
PL - Polonia 38
GR - Grecia 34
RO - Romania 33
TR - Turchia 30
SE - Svezia 28
ZA - Sudafrica 27
FI - Finlandia 24
NO - Norvegia 24
BE - Belgio 21
TW - Taiwan 21
MX - Messico 20
PH - Filippine 20
RS - Serbia 20
NZ - Nuova Zelanda 17
BG - Bulgaria 16
CL - Cile 16
DK - Danimarca 16
PT - Portogallo 16
BD - Bangladesh 15
HK - Hong Kong 15
SA - Arabia Saudita 15
AR - Argentina 14
TH - Thailandia 14
IE - Irlanda 13
PK - Pakistan 13
EG - Egitto 12
MY - Malesia 12
VN - Vietnam 12
HU - Ungheria 11
IL - Israele 9
IR - Iran 9
AT - Austria 8
CO - Colombia 8
SG - Singapore 8
AE - Emirati Arabi Uniti 6
OM - Oman 6
SZ - Regno dello Swaziland 6
BY - Bielorussia 5
CR - Costa Rica 4
KH - Cambogia 4
KP - Corea 4
LV - Lettonia 4
MT - Malta 4
EC - Ecuador 3
EE - Estonia 3
HR - Croazia 3
NI - Nicaragua 3
PE - Perù 3
SK - Slovacchia (Repubblica Slovacca) 3
GH - Ghana 2
IS - Islanda 2
LB - Libano 2
LU - Lussemburgo 2
MA - Marocco 2
NG - Nigeria 2
SI - Slovenia 2
A1 - ???statistics.table.value.countryCode.A1??? 1
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AX - Isole di terra 1
CU - Cuba 1
CY - Cipro 1
GE - Georgia 1
GN - Guinea 1
IQ - Iraq 1
KE - Kenya 1
KZ - Kazakistan 1
LK - Sri Lanka 1
MD - Moldavia 1
ME - Montenegro 1
SY - Repubblica araba siriana 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
VE - Venezuela 1
Totale 8464
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Città #
Fairfield 473
Seattle 339
Woodbridge 293
Houston 239
Ashburn 238
Buffalo 223
Cambridge 210
Milan 198
Mountain View 193
Wilmington 181
Ann Arbor 114
Wuhan 94
Beijing 91
University Park 81
Ottawa 51
Phoenix 47
Nürnberg 44
Redmond 43
Shanghai 35
Las Vegas 34
Tokyo 32
Hangzhou 30
Kiez 30
Rome 27
London 24
Nanjing 22
Toronto 22
Clearwater 19
Bangalore 18
New York 17
Rotterdam 17
Chicago 16
Muizenberg 16
Nijmegen 16
Philadelphia 16
Jakarta 15
Southend 15
Pietra Ligure 14
San Diego 14
Athens 13
Munich 13
Taipei 13
Atlanta 12
Duncan 12
Henderson 12
Paris 12
Serra 12
Evanston 11
Mcallen 11
Scranton 11
Conshohocken 10
Easton 10
Hanoi 10
Menlo Park 10
Montréal 10
Beograd 9
Columbus 9
Dearborn 9
Glasgow 9
Los Angeles 9
Middlesbrough 9
New Delhi 9
Québec 9
Riva 9
Rochester 9
Sydney 9
Verona 9
Arlington 8
Boston 8
Brampton 8
Gurgaon 8
Liverpool 8
Milpitas 8
Moscow 8
Salt Lake City 8
San Jose 8
Seoul 8
Amsterdam 7
Austin 7
Belgrade 7
Costa Mesa 7
Dallas 7
Hebei 7
Indianapolis 7
Napoli 7
Norwalk 7
Olomouc 7
Polska 7
Saint Louis 7
San Francisco 7
Shenyang 7
Urbana 7
Warsaw 7
Auckland 6
Birmingham 6
Brisbane 6
Bucharest 6
Chengdu 6
Durham 6
Fremont 6
Totale 4125
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Nome #
Therapy in myotonic disorders and in muscle channelopathies, file 256490 714
Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2, file 276147 687
Treatment for periodic paralysis, file 256466 609
Cerebral involvement in myotonic dystrophies, file 252798 503
Concurrence of facioscapulohumeral muscular dystrophy and myasthenia gravis, file 252755 357
Computerized tomography and magnetic resonance muscle imaging in Miyoshi's myopathy, file 256419 340
Electromechanical delay components during skeletal muscle contraction and relaxation in patients with myotonic dystrophy type 1, file 446319 338
Reduced cerebral blood flow and impaired visual-spatial function in proximal myotonic myopathy, file 252732 316
Cognitive impairment in adult myotonic dystrophies : a longitudinal study, file 256405 302
Andersen's syndrome : a distinct periodic paralysis, file 256496 281
Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect, file 256480 275
A newly-described myotonic disorder (proximal myotonic myopathy--PROMM): personal experience and review of the literature, file 256504 203
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion, file 252803 197
Mutation in the S4 segment of the adult skeletal sodium channel gene in an Italian paramyotonia congenita (PC) family, file 256508 197
Hypokalemic periodic paralysis in a patient with acquired growth hormone deficiency, file 252787 196
Quantitative myotonia assessment: an experimental protocol, file 252736 195
Oculopharyngeal muscular dystrophy in Italy., file 252725 175
A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies, file 256399 167
Deregulated MicroRNAs in Myotonic Dystrophy Type 2, file 214691 162
Increased visceral adipose tissue rather than BMI as a risk factor for dementia, file 252793 159
Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2, file 252768 154
Randomized, placebo-controlled trials of dichlorphenamide in periodic paralysis, file 699597 143
Persistent autobiographical amnesia: a case report, file 256474 137
Premature senescence in primary muscle cultures of myotonic dystrophy type 2 is not associated with p16 induction, file 355573 134
Long-term follow-up free of ventricular fibrillation recurrence after resuscitated cardiac arrest in a myotonic dystrophy type 1 patient, file 240911 133
Stable hybrid myotubes: a new model for studying re-expression of enzymatic activities in vitro, file 256506 127
RBFOX1 cooperates with MBNL1 to control splicing in muscle, including events altered in myotonic dystrophy type 1, file 355533 123
Glucose metabolism and dopamine PET correlates in a patient with myotonic dystrophy type 2 and parkinsonism, file 252765 121
Genome wide identification of aberrant alternative splicing events in myotonic dystrophy type 2, file 355215 119
Validation of plasma microRNAs as biomarkers for myotonic dystrophy type 1, file 779358 105
Clinical spectrum of proximal myotonic myopathy (PROMM) syndrome, file 256437 102
"I know that you know that I know" : Neural substrates associated with social cognition deficits in DM1 patients, file 699609 97
Overexpression of CUGBP1 in Skeletal Muscle from Adult Classic Myotonic Dystrophy Type 1 but Not from Myotonic Dystrophy Type 2, file 355152 96
Reduction of toxic RNAs in myotonic dystrophies type 1 and type 2 by the RNA helicase p68/DDX5, file 662801 94
The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C-terminal peptide of the ClC-1 channel, file 1157527 93
Brain Connectomics' Modification to Clarify Motor and Nonmotor Features of Myotonic Dystrophy Type 1, file 675077 93
RNA transcription and maturation in skeletal muscle cells are similarly impaired in myotonic dystrophy and sarcopenia : the ultrastructural evidence, file 355562 84
Tibialis anterior muscle needle biopsy and sensitive biomolecular methods : a useful tool in myotonic dystrophy type 1, file 666174 83
Receptor and post-receptor abnormalities contribute to insulin resistance in myotonic dystrophy type 1 and type 2 skeletal muscle, file 904846 82
Myotonic dystrophies : state of the art of new therapeutic developments for the CNS, file 904829 79
Neuropsychological and psychological functioning aspects in myotonic dystrophy type 1 patients in Italy, file 1170438 76
Clinical aspects, molecular pathomechanisms and management of myotonic dystrophies, file 355177 63
Mexiletine Improves Symptoms and Signs of Myotonia in Non-dystrophic Myotonia, file 249014 57
Status update and interim results from the Asymptomatic Carotid Surgery Trial-2 (ACST-2), file 769180 53
Andersen’s syndrome: a single or multiple gene channelopathy?, file 252721 52
Clinical factors associated with statins prescription in acute ischemic stroke patients : findings from the Lombardia Stroke Registry, file 328588 36
Contrast-induced seizures after cardiac catheterization in a 6-year-old child, file 252770 34
Rare Disease : Cardiac Risk Assessment With MRI in Patients With Myotonic Dystrophy Type 1, file 1490599 20
Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4, file 1580584 19
Circulating irisn is reduced in male patients with type 1 and type 2 Myotonic Dystrophies, file 925768 17
Consensus-based care recommendations for adults with myotonic dystrophy type 1., file 1372870 15
SCN4A mutation as modifying factor of myotonic dystrophy type 2 phenotype, file 447469 9
Slowly progressing varicella zoster brainstem encephalitis complicating Ramsay Hunt syndrome in an immunocompetent patient : case report and review of the literature, file 904841 9
Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2, file 252819 7
Myotonia congenita : novel mutations in CLCN1 gene and functional characterizations in Italian patients, file 252823 6
Peripheral fatigue in patients with myotonic dystrophy type 1: an EMG, MMG and force combined approach, file 477822 6
Myotonic dystrophy type 2 and modifier genes : an update on clinical and pathomolecular aspects, file 779370 6
Biomolecular diagnosis of myotonic dystrophy type 2 : a challenging approach, file 904834 6
Biomolecular identification of (CCTG)n mutation in myotonic dystrophy type 2 (DM2) by FISH on muscle biopsy, file 252760 5
Vitamin D, parathyroid hormone and muscle impairment in myotonic dystrophies, file 281921 5
Clinical Reasoning : a 35-year-old woman with hyperstartling, stiffness, and accidental falls : a startling diagnosis, file 779382 5
Posterior reversible encephalopathy syndrome after long-term treatment with low-dose sunitinib : a case report, file 904822 5
Posterior reversible encephalopathy syndrome after long-term treatment with low-dose sunitinib : a case report, file 910037 5
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome), file 252741 4
Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1(DM-1) and in proximal myotonic myopathy (PROMM/DM-2), file 252750 4
Gonadal failure is associated with visceral adiposity in myotonic dystrophies, file 557275 4
A novel Ile1455Thr variant in the skeletal muscle sodium channel alpha-subunit in a patient with a severe adult-onset proximal myopathy with electrical myotonia and a patient with mild paramyotonia phenotype, file 779365 4
Myotonic dystrophy type 2 and modifier genes : an update on clinical and pathomolecular aspects, file 832552 4
The frequency and severity of cardiac involvement in myotonic dystrophy type 2 (DM2) : long-term outcomes, file 1002203 3
The role of clinical and neuroimaging features in the diagnosis of CADASIL, file 1108263 3
Fragility fractures and bone mineral density in male patients affected by type 1 and type 2 myotonic dystrophy, file 1379017 3
Muscle glucose-6-phosphate dehydrogenase deficiency: restoration of enzymatic activity in hybrid myotubes, file 252708 3
Neural regulation of acid maltase in an unusual adult onset deficiency, file 252712 3
Proximal myotonic myopathy : a syndrome with a favourable prognosis?, file 252744 3
Proximal myotonic dystrophy mimicking progressive muscular atrophy, file 252763 3
Myotonic dystrophy is not only a disease affecting the muscles, it is also a CNS disorder, file 307851 3
Electromechanical delays during a fatiguing exercise and recovery in patients with myotonic dystrophy type 1, file 832541 3
null, file 1087083 2
The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C-terminal peptide of the ClC-1 channel, file 1204886 2
Muscle biopsy and cell cultures: potential diagnostic tools in hereditary skeletal muscle channelopathies, file 252758 2
Identification and Characterization of DM1 Patients by a New Diagnostic Certified Assay: Neuromuscular and Cardiac Assessments, file 281920 2
Electromechanical delay components during skeletal muscle contraction and relaxation in patients with myotonic dystrophy type 1, file 477833 2
A novel Ile1455Thr variant in the skeletal muscle sodium channel alpha-subunit in a patient with a severe adult-onset proximal myopathy with electrical myotonia and a patient with mild paramyotonia phenotype, file 832522 2
Report of the third outcome measures in myotonic dystrophy type 1 (OMMYD-3) international workshop Paris, France, June 8, 2015, file 1373542 1
Cultures myoblasts from patients affected by myotonic dystropy type 2 exhibit senescence-related features: ultrastructural evidence, file 461202 1
Muscle histopathology in a large cohor of 65 italian DM2 patients: diagnostic role and pitfalls of ribonuclear inclusions, file 461219 1
Characterization of sarcoplasmic reticulum Ca2+ ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathy, file 699593 1
Drug resistant focal epilepsy in a patient with myotonic dystrophy type 2 : casual or causal association?, file 699601 1
Cognition in myotonic dystrophy type 1: a 5-year follow-up study, file 699605 1
High-sensitive cardiac troponin T (hs-cTnT) assay as serum biomarker to predict cardiac risk in myotonic dystrophy : A case-control study, file 779346 1
Clusters of cognitive impairment among different phenotypes of myotonic dystrophy type 1 and type 2, file 779354 1
Totale 9155
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Categoria #
all - tutte 9155
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 9155
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2015/2016200 0000 00 3635 51372120
2016/20171075 664946420 3232 3047 235223246
2017/2018783 55604987 5761 4163 81647095
2018/20191700 891328095 100113 103111 144244263226
2019/20202507 198156147369 222227 228242 259149151159
2020/20211169 105228129232 176167 1320 0000
Totale 9155
 
 
 
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