IRIS
POLITANO, Luisa
 Distribuzione geografica
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Continente #
EU - Europa 10.553
NA - Nord America 7.614
AS - Asia 5.637
SA - Sud America 1.113
AF - Africa 74
Continente sconosciuto - Info sul continente non disponibili 10
OC - Oceania 10
Totale 25.011
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Nazione #
US - Stati Uniti d'America 7.508
RU - Federazione Russa 4.007
SG - Singapore 2.144
IE - Irlanda 2.038
HK - Hong Kong 1.187
CN - Cina 1.170
UA - Ucraina 1.069
BR - Brasile 959
GB - Regno Unito 879
DE - Germania 591
IT - Italia 573
FR - Francia 376
VN - Vietnam 339
SE - Svezia 318
FI - Finlandia 291
TR - Turchia 230
GR - Grecia 178
IN - India 154
KR - Corea 145
JP - Giappone 67
AR - Argentina 63
AT - Austria 57
CA - Canada 53
BD - Bangladesh 41
BE - Belgio 37
ES - Italia 37
ID - Indonesia 34
MX - Messico 30
ZA - Sudafrica 30
EC - Ecuador 29
NL - Olanda 23
IQ - Iraq 21
CO - Colombia 18
CZ - Repubblica Ceca 18
UZ - Uzbekistan 16
PK - Pakistan 12
PL - Polonia 12
PY - Paraguay 11
CL - Cile 10
MA - Marocco 10
PT - Portogallo 9
AE - Emirati Arabi Uniti 8
EU - Europa 8
VE - Venezuela 8
EG - Egitto 7
HN - Honduras 7
KE - Kenya 6
KZ - Kazakistan 6
LB - Libano 6
PE - Perù 6
SA - Arabia Saudita 6
CH - Svizzera 5
IL - Israele 5
JM - Giamaica 5
NP - Nepal 5
NZ - Nuova Zelanda 5
RO - Romania 5
RS - Serbia 5
UY - Uruguay 5
AU - Australia 4
CY - Cipro 4
DO - Repubblica Dominicana 4
ET - Etiopia 4
IS - Islanda 4
JO - Giordania 4
KG - Kirghizistan 4
KW - Kuwait 4
LT - Lituania 4
OM - Oman 4
SC - Seychelles 4
AL - Albania 3
BO - Bolivia 3
TN - Tunisia 3
TT - Trinidad e Tobago 3
AZ - Azerbaigian 2
BB - Barbados 2
DK - Danimarca 2
EE - Estonia 2
GA - Gabon 2
GE - Georgia 2
HR - Croazia 2
LK - Sri Lanka 2
MY - Malesia 2
PH - Filippine 2
PS - Palestinian Territory 2
XK - ???statistics.table.value.countryCode.XK??? 2
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BH - Bahrain 1
BJ - Benin 1
BN - Brunei Darussalam 1
BY - Bielorussia 1
CG - Congo 1
CI - Costa d'Avorio 1
CM - Camerun 1
HU - Ungheria 1
IR - Iran 1
KH - Cambogia 1
LV - Lettonia 1
Totale 24.996
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Città #
Dublin 2.036
Jacksonville 1.647
Moscow 1.232
Hong Kong 1.181
Chandler 1.008
Santa Clara 878
Singapore 747
Dallas 425
Princeton 316
Medford 248
Roxbury 195
Ann Arbor 183
Boardman 180
Wilmington 148
Seoul 144
Hefei 138
Beijing 133
San Mateo 128
Woodbridge 127
Ashburn 117
Bengaluru 112
Bremen 111
Ho Chi Minh City 105
Cambridge 90
Caserta 90
The Dalles 87
São Paulo 70
Dong Ket 66
Hanoi 60
Des Moines 58
Mountain View 52
New York 46
Düsseldorf 43
Munich 43
Houston 39
Jinan 35
Nuremberg 32
Vienna 32
Los Angeles 30
Brussels 28
Guangzhou 27
Nanjing 27
Norwalk 24
Rio de Janeiro 24
Rome 24
Auburn Hills 23
Tianjin 23
Helsinki 22
Milan 22
Redwood City 22
Belo Horizonte 21
Naples 20
Hangzhou 19
London 19
Nanchang 18
Hebei 17
Shenyang 16
West Jordan 16
Zhengzhou 16
Curitiba 15
Taiyuan 15
Tashkent 15
Napoli 14
São José dos Campos 14
Brasília 13
Haikou 13
Haiphong 13
Johannesburg 13
Porto Alegre 13
Santiago de Compostela 13
Jakarta 12
Boston 11
Changsha 11
Chicago 11
Columbus 11
Frankfurt am Main 11
Guarulhos 11
Ottawa 11
Quito 11
Salvador 11
Toronto 11
Venice 11
Asunción 10
Campinas 10
Jiaxing 10
Shanghai 10
Shenzhen 10
Taizhou 10
Amsterdam 9
Brno 9
Brooklyn 9
Recife 9
San Francisco 9
Trieste 9
Warsaw 9
Atlanta 8
Baghdad 8
Da Nang 8
Lanzhou 8
Manaus 8
Totale 13.287
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Nome #
1) Study of myocardial perfusion with Tl-201 in patients affected by Duchenne's/Becker's muscolar dystrophy 407
1) Comparison between SPECT myocardical scintigraphy with 201Tl and 99mTc-MIBI in patients affected by Duchenne's dystrophy 394
IperCKemia asintomatica. Quando e perchè fare l'indagine genetica 151
A report on 528 intragenic deletions detected in DMD and BMD patients by an Italian collaborative study 133
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes 127
ACE inhibition to slow progression of myocardial fibrosis in muscular dystrophies 123
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients. 122
"I have got something positive out of this situation": psychological benefits of caregiving in relatives of young people with muscular dystrophy. 120
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene 120
Current therapeutic guidelines in Duchenne Muscular Dystrophy to prolong life. 119
Cardiomyopathies associated with Muscular Dystrophies 118
Novel small mutations along the DMD/BMD gene associated with different phenotypes 116
Novel mutations in LMNA A/C gene and associated phenotypes 116
Autonomic nervous system imbalance and left ventricular systolic dysfunction as potential candidates for arrhythmogenesis in Becker muscular dystrophy 114
P-wave duration and dispersion in patients with Emery-Dreifuss muscular dystrophy. 114
A Unique Myopathy Syndrome in a Patient Disclosing Clinical, Laboratory, and Genetic Findings of Late-Onset Pompe Disease, Together with a Lack of Dysferlin on Muscle Biopsy 114
Autosomal dominant Ullrich congenital muscular dystrophy due to a de novo mutation in COL6A3 gene. A case report 112
Dispositivo per la valutazione del test del cammino dei 6 minuti 112
Regional and transmural dispersion of repolarisation in patients with Emery-Dreifuss muscular dystrophy. 111
The effect of atrial preference pacing on atrial fibrillation electrophysiological substrate in Myotonic Dystrophy type 1 population. 110
A preliminary randomized study of growth hormone administration in Becker and Duchenne muscular dystrophies 110
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein 109
Right atrial appendage versus Bachmann's bundle stimulation: a two-year comparative study of electrical parameters in myotonic dystrophy type-1 patients. 108
SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin function 108
Double carrier status in CANP3 and beta-sarcoglycan genes results in a mild disease phenotype 108
Identification of the Syrian hamster cardiomyopathy gene 107
P dispersion: a new electrocardiographic parameter to evaluate the risk of atrial arrhythmias in Emery-Dreifuss muscular dystrophies 107
G.O.7 Multiple genetic variations in limb-girdle muscular dystrophies 107
High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithm 106
Early onset of cardiomyopathy and primary prevention of sudden death in X-linked Emery-Dreifuss muscular dystrophy. 106
Dystrophin gene scanning by DHPLC of DMD carriers without deletions or duplications 106
Paroxysmal atrial fibrillation in myotonic dystrophy type 1 patients: P wave duration and dispersion analysis. 105
Are there real benefits to implanting cardiac devices in patients with end-stage dilated dystrophinopathic cardiomyopathy? Review of literature and personal results 105
Does Bachmann's bundle pacing prevent atrial fibrillation in myotonic dystrophy type 1 patients? A 12 months follow-up study 104
Risk of arrhythmias in MYotonic Dystrophy: trial design of the RAMYD study 103
Dispositivo per la valutazione del test del "cammino dei sei minuti (six minutes walking test)" 103
Atrial fibrillation burden in Myotonic Dystrophy type 1 patients implanted with dual chamber pacemaker: the efficacy of the overdrive atrial algorithm at 2 year follow-up. 102
24 month longitudinal data in ambulant boys with D uchenne muscular dystrophy. 102
A novel homozygous beta-sarcoglycan gene mutation: case description. 102
Aspetti clinici, genetici ed epidemiologici delleDistrofie muscolari dei Cingoli nel Sud Italia 102
Multiple heterozygosity for different muscle genes is not rare among individuals with pauci-symptomatic hyperCKemia 102
P2.27 Full exome resequencing by next generation sequencing (NGS) combined with chip analysis for the genetic testing of unclassified myopathic patients 102
Clinical features of patients with dystrophinopathy sharing the 45-55 exon deletion of DMD gene 102
The effect of atrial preference pacing on paroxysmal atrial fibrillation incidence in myotonic dystrophy type 1 patients: a prospective, randomized, single-bind cross-over study. 101
Gene redundancies in the dystrophin-associated protein complex 101
6 Min walk test 12 month changes in DMD: correlation with the genotype 101
Italian validation of INQoL, a quality of life questionnaire for adults with muscle diseases 100
Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies 100
6 minute walk test in Duchenne MD patients with different mutations: 12 month changes 100
Affinity proteomics within rare diseases: a BIO-NMD study for blood biomarkers of muscular dystrophies 100
Burden, professional support, and social network in families of children and young adults with muscular dystrophies. 99
Does a high percentage of right ventricular pacing influence the incidence of paroxysmal atrial fibrillation in myotonic dystrophy type 1 patients? 99
Analysis of caveolin-3 (CAV-3) gene in patients with limb-girdle muscular dystrophies and/or isolated hyperCKemia 99
Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy 97
Alu-Mediated Insertions in the DMD Gene: A Difficult Puzzle to Interpret Clinically 97
Effects of growth hormone therapy in Becker patients with dilated cardiomyopathy 97
Acta Myologica (myopathies, cardiomyopathies and neuromyopathies) 97
42nd ENMC Sponsored International Workshop: X-linked Cardiomyopathies 97
Efficacy and safety of ropivacaine HCl in peribulbar anaesthesia for cataract surgery in patients with myotonic dystrophy type 1 97
Nusinersen safety and effects on motor function in adult spinal muscular atrophy type 2 and 3 97
X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sample 96
Familial dilated cardiomyopathy associated with the typical dystrophin BMD mutation. Report on two additional cases 96
P.P.6 02 Cardiac and respiratory involvement in autosomal recessive limb-girdle muscular dystrophies 96
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy 95
Usefulness of Heart Rate Variability as a predictor of sudden cardiac death in muscular dystrophies 95
X chromosome inactivation pattern in Duchenne muscular dystrophy carriers 95
Skewed X-chromosome inactivation plays a crucial role in the onset of symptoms in carriers of Becker muscular dystrophy. 95
Le Distrofie dei Cingoli autosomiche recessive: calpainopatie e disferlinopatie 94
Evaluation of cardiac and respiratory involvement in sarcoglycanopathies 94
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease 94
Next generation sequencing applications are ready for genetic diagnosis of muscular dystrophies. 94
Early onset "electrical" heart failure in myotonic dystrophy type 1 patient: the role of ICD biventricular pacing. 93
Optimal site for atrial lead implantation in myotonic dystrophy patients: the role of Bachmann's Bundle stimulation 93
Growth hormone deficiency in patients with Duchenne/Becker muscular dystrophy: association with dilated cardiomyopathy 93
Managing dystrophinopathic cardiomyopathy 93
Increased heterogeneity of ventricular repolarization in myotonic dystrophy type 1 population 93
Advances in basic and clinical research in laminopathies. 92
Miocardiopatie e miopatie infiammatorie. 92
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 92
238th ENMC International Workshop: Updating management recommendations of cardiac dystrophinopathyHoofddorp, The Netherlands, 30 November - 2 December 2018. 92
Molecular and Muscle Pathology in a series of Caveolinopathy patients 91
Successful combined prenatal diagnosis for Duchenne and facio-scapulo- humeral dystrophies 91
A novel mutation in CPT2 gene in two unrelated patients from Campania region 91
Arrhythmic risk in Steinert Disease 91
Stydy of anti Mullerian hormone levels in patients with myotonic dystrophy type 1. Prelilminary results. 91
The position of nonsense mutations can predict the phenotype severity: A survey on the DMD gene 91
Clinical and genetic findings in sarcoglycanopathies 90
Heart transplantation in patients with dystrophinopathic cardiomyopathy: Review of the literature and personal series 90
Right atrial preference pacing algorithm in the prevention of paroxysmal atrial fibrillation in myotonic dystrophy type 1 patients: a long term follow-up study. 89
Far field R-wave sensing in Myotonic Dystrophy type 1: right atrial appendage versus Bachmann's bundle region lead placement. 89
Evaluation of the cardiomyopathy in Becker muscular dystrophy 89
Dysferlinopathy presenting as facio-scapulo-humeral dystrophy 89
The QT dispersion in the risk stratification of sudden death in Becker patients 89
The Role of TRPM4 Gene Mutations in Causing Familial Progressive Cardiac Conduction Disease: A Further Contribution 89
Unusual association of Kallmann syndrome with empty sella and arachnoid cyst 88
Heart involvement in Emery-Dreifuss muscular dystrophies: new parameters to detect early atrial fibrosis and vulnerability 88
Assessment of Upper Limb function in DMD patients: Comparison with normative data 88
Intraocular pressure in patients with muscular dystrophies 87
Anterior capsule phimosis and capsular block syndrome in a patient with Steinert myotonic dystrophy: A case report 87
Il trattamento chirurgico delle scoliosi nella Distrofia Muscolare di Duchenne. 87
Totale 10.710
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Categoria #
all - tutte 101.172
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 101.172
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.280 0 0 0 0 0 11 308 272 14 308 230 137
2021/20221.919 138 14 32 44 701 11 22 50 57 159 143 548
2022/20233.815 366 98 25 318 390 296 21 214 1.893 26 77 91
2023/20241.332 114 59 60 128 526 51 13 25 8 20 90 238
2024/20254.168 21 24 44 93 606 437 547 367 620 873 312 224
2025/20267.942 533 673 1.046 886 1.346 3.458 0 0 0 0 0 0
Totale 25.413