IRIS
POLITANO, Luisa
 Distribuzione geografica
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Continente #
EU - Europa 17.708
NA - Nord America 11.372
AS - Asia 6.665
SA - Sud America 1.162
Continente sconosciuto - Info sul continente non disponibili 417
AF - Africa 89
OC - Oceania 12
Totale 37.425
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Nazione #
US - Stati Uniti d'America 11.148
RU - Federazione Russa 10.473
SG - Singapore 2.615
IE - Irlanda 2.039
CN - Cina 1.329
HK - Hong Kong 1.212
UA - Ucraina 1.073
IT - Italia 1.049
BR - Brasile 989
GB - Regno Unito 928
DE - Germania 618
VN - Vietnam 602
FR - Francia 398
FI - Finlandia 353
SE - Svezia 321
TR - Turchia 232
IN - India 179
GR - Grecia 178
KR - Corea 157
CA - Canada 114
JP - Giappone 87
AR - Argentina 70
AT - Austria 57
BD - Bangladesh 56
ES - Italia 40
ID - Indonesia 38
BE - Belgio 37
MX - Messico 36
NL - Olanda 33
ZA - Sudafrica 33
EC - Ecuador 31
CO - Colombia 24
IQ - Iraq 23
CZ - Repubblica Ceca 20
JM - Giamaica 18
PL - Polonia 18
UZ - Uzbekistan 18
PK - Pakistan 16
HN - Honduras 12
CH - Svizzera 11
CL - Cile 11
MA - Marocco 11
PH - Filippine 11
PT - Portogallo 11
PY - Paraguay 11
CR - Costa Rica 10
AE - Emirati Arabi Uniti 9
EE - Estonia 9
EG - Egitto 9
VE - Venezuela 9
EU - Europa 8
LT - Lituania 8
RO - Romania 8
KE - Kenya 7
KZ - Kazakistan 7
PE - Perù 7
SA - Arabia Saudita 7
AU - Australia 6
GT - Guatemala 6
JO - Giordania 6
LB - Libano 6
NP - Nepal 6
RS - Serbia 6
BB - Barbados 5
ET - Etiopia 5
IL - Israele 5
NZ - Nuova Zelanda 5
SC - Seychelles 5
TH - Thailandia 5
TN - Tunisia 5
TT - Trinidad e Tobago 5
UY - Uruguay 5
BO - Bolivia 4
CY - Cipro 4
DO - Repubblica Dominicana 4
IS - Islanda 4
KG - Kirghizistan 4
KW - Kuwait 4
OM - Oman 4
AL - Albania 3
GE - Georgia 3
MY - Malesia 3
PR - Porto Rico 3
AZ - Azerbaigian 2
BH - Bahrain 2
BS - Bahamas 2
CI - Costa d'Avorio 2
DK - Danimarca 2
DZ - Algeria 2
GA - Gabon 2
HR - Croazia 2
LK - Sri Lanka 2
MD - Moldavia 2
NI - Nicaragua 2
PS - Palestinian Territory 2
QA - Qatar 2
SV - El Salvador 2
TW - Taiwan 2
XK - ???statistics.table.value.countryCode.XK??? 2
AM - Armenia 1
Totale 36.992
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Città #
Moscow 3.676
Dublin 2.037
Jacksonville 1.648
Hong Kong 1.203
Singapore 1.013
Chandler 1.008
Santa Clara 991
Ashburn 795
San Jose 794
Council Bluffs 666
Dallas 446
Princeton 335
Medford 248
Milan 201
Roxbury 195
Ho Chi Minh City 189
Ann Arbor 183
Boardman 181
Beijing 155
Seoul 155
Wilmington 148
Hefei 138
San Mateo 128
Woodbridge 127
Hanoi 117
Bengaluru 112
Bremen 111
Caserta 91
Cambridge 90
The Dalles 87
Helsinki 82
New York 79
São Paulo 72
Dong Ket 66
Miano 60
Des Moines 59
Los Angeles 52
Mountain View 52
Houston 49
Düsseldorf 43
Munich 43
Atlanta 37
Rome 36
Frankfurt am Main 35
Jinan 35
Nuremberg 32
Vienna 32
Chicago 29
Da Nang 29
Guangzhou 29
Brussels 28
Rio de Janeiro 28
Nanjing 27
Haiphong 26
Naples 26
North Bergen 26
London 24
Norwalk 24
Auburn Hills 23
Orem 23
Tianjin 23
Redwood City 22
Tokyo 22
Belo Horizonte 21
Montreal 20
Hangzhou 19
Memphis 18
Nanchang 18
Toronto 18
Brooklyn 17
Hebei 17
Tashkent 17
Curitiba 16
Phoenix 16
Shenyang 16
West Jordan 16
Zhengzhou 16
Amsterdam 15
Brasília 15
Johannesburg 15
Philadelphia 15
Taiyuan 15
Boston 14
Buffalo 14
Carrboro 14
Chennai 14
Denver 14
Napoli 14
San Francisco 14
São José dos Campos 14
Columbus 13
Haikou 13
Jakarta 13
Kingston 13
Miami 13
Porto Alegre 13
Quito 13
Santiago de Compostela 13
Warsaw 13
Florence 12
Totale 19.102
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Nome #
1) Study of myocardial perfusion with Tl-201 in patients affected by Duchenne's/Becker's muscolar dystrophy 501
1) Comparison between SPECT myocardical scintigraphy with 201Tl and 99mTc-MIBI in patients affected by Duchenne's dystrophy 491
Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature 196
IperCKemia asintomatica. Quando e perchè fare l'indagine genetica 189
A report on 528 intragenic deletions detected in DMD and BMD patients by an Italian collaborative study 187
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes 187
Autosomal dominant Ullrich congenital muscular dystrophy due to a de novo mutation in COL6A3 gene. A case report 175
"I have got something positive out of this situation": psychological benefits of caregiving in relatives of young people with muscular dystrophy. 175
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients. 175
ACE inhibition to slow progression of myocardial fibrosis in muscular dystrophies 173
Identification of the Syrian hamster cardiomyopathy gene 172
Current therapeutic guidelines in Duchenne Muscular Dystrophy to prolong life. 172
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene 172
Novel small mutations along the DMD/BMD gene associated with different phenotypes 170
P-wave duration and dispersion in patients with Emery-Dreifuss muscular dystrophy. 168
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 168
Autonomic nervous system imbalance and left ventricular systolic dysfunction as potential candidates for arrhythmogenesis in Becker muscular dystrophy 163
Alu-Mediated Insertions in the DMD Gene: A Difficult Puzzle to Interpret Clinically 158
Dispositivo per la valutazione del test del cammino dei 6 minuti 158
Does a high percentage of right ventricular pacing influence the incidence of paroxysmal atrial fibrillation in myotonic dystrophy type 1 patients? 157
Regional and transmural dispersion of repolarisation in patients with Emery-Dreifuss muscular dystrophy. 157
P dispersion: a new electrocardiographic parameter to evaluate the risk of atrial arrhythmias in Emery-Dreifuss muscular dystrophies 157
G.O.7 Multiple genetic variations in limb-girdle muscular dystrophies 157
Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy 155
Right atrial appendage versus Bachmann's bundle stimulation: a two-year comparative study of electrical parameters in myotonic dystrophy type-1 patients. 155
P2.27 Full exome resequencing by next generation sequencing (NGS) combined with chip analysis for the genetic testing of unclassified myopathic patients 155
Are there real benefits to implanting cardiac devices in patients with end-stage dilated dystrophinopathic cardiomyopathy? Review of literature and personal results 155
A preliminary randomized study of growth hormone administration in Becker and Duchenne muscular dystrophies 154
Novel mutations in LMNA A/C gene and associated phenotypes 154
Cardiomyopathies associated with Muscular Dystrophies 154
Double carrier status in CANP3 and beta-sarcoglycan genes results in a mild disease phenotype 154
Aspetti clinici, genetici ed epidemiologici delleDistrofie muscolari dei Cingoli nel Sud Italia 154
Does Bachmann's bundle pacing prevent atrial fibrillation in myotonic dystrophy type 1 patients? A 12 months follow-up study 153
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein 153
Gene redundancies in the dystrophin-associated protein complex 153
24 month longitudinal data in ambulant boys with D uchenne muscular dystrophy. 152
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. 151
The effect of atrial preference pacing on atrial fibrillation electrophysiological substrate in Myotonic Dystrophy type 1 population. 151
P.P.6 02 Cardiac and respiratory involvement in autosomal recessive limb-girdle muscular dystrophies 151
Analysis of caveolin-3 (CAV-3) gene in patients with limb-girdle muscular dystrophies and/or isolated hyperCKemia 150
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease 149
Paroxysmal atrial fibrillation in myotonic dystrophy type 1 patients: P wave duration and dispersion analysis. 148
Early onset of cardiomyopathy and primary prevention of sudden death in X-linked Emery-Dreifuss muscular dystrophy. 148
Dystrophin gene scanning by DHPLC of DMD carriers without deletions or duplications 148
The position of nonsense mutations can predict the phenotype severity: A survey on the DMD gene 148
SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin function 147
Optimal site for atrial lead implantation in myotonic dystrophy patients: the role of Bachmann's Bundle stimulation 147
Nusinersen safety and effects on motor function in adult spinal muscular atrophy type 2 and 3 147
A novel homozygous beta-sarcoglycan gene mutation: case description. 146
Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies 145
Multiple heterozygosity for different muscle genes is not rare among individuals with pauci-symptomatic hyperCKemia 145
Acta Myologica (myopathies, cardiomyopathies and neuromyopathies) 144
6 Min walk test 12 month changes in DMD: correlation with the genotype 144
Evaluation of the cardiomyopathy in Becker muscular dystrophy 142
Efficacy and safety of ropivacaine HCl in peribulbar anaesthesia for cataract surgery in patients with myotonic dystrophy type 1 142
Increased heterogeneity of ventricular repolarization in myotonic dystrophy type 1 population 140
238th ENMC International Workshop: Updating management recommendations of cardiac dystrophinopathyHoofddorp, The Netherlands, 30 November - 2 December 2018. 140
Right atrial preference pacing algorithm in the prevention of paroxysmal atrial fibrillation in myotonic dystrophy type 1 patients: a long term follow-up study. 139
Risk of arrhythmias in MYotonic Dystrophy: trial design of the RAMYD study 139
6 minute walk test in Duchenne MD patients with different mutations: 12 month changes 139
Bi-Allelic DES Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac Function 138
High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithm 138
Burden, professional support, and social network in families of children and young adults with muscular dystrophies. 138
X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sample 138
Far field R-wave sensing in Myotonic Dystrophy type 1: right atrial appendage versus Bachmann's bundle region lead placement. 138
Familial dilated cardiomyopathy associated with the typical dystrophin BMD mutation. Report on two additional cases 138
X chromosome inactivation pattern in Duchenne muscular dystrophy carriers 138
Advances in basic and clinical research in laminopathies. 137
42nd ENMC Sponsored International Workshop: X-linked Cardiomyopathies 137
Skewed X-chromosome inactivation plays a crucial role in the onset of symptoms in carriers of Becker muscular dystrophy. 137
Clinical features of patients with dystrophinopathy sharing the 45-55 exon deletion of DMD gene 137
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 136
Managing dystrophinopathic cardiomyopathy 136
G.P.4.03 Mutations in the lamin A/C gene: An emergent cause of fatal arrhythmias in congenital muscular dystrophies 136
Adults with spinal muscular atrophy: a large-scale natural history study shows gender effect on disease 134
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. 134
Affinity proteomics within rare diseases: a BIO-NMD study for blood biomarkers of muscular dystrophies 134
Arrhythmic risk in Steinert Disease 134
The Role of TRPM4 Gene Mutations in Causing Familial Progressive Cardiac Conduction Disease: A Further Contribution 134
Early onset "electrical" heart failure in myotonic dystrophy type 1 patient: the role of ICD biventricular pacing. 133
Evaluation of cardiac and respiratory involvement in sarcoglycanopathies 133
Usefulness of Heart Rate Variability as a predictor of sudden cardiac death in muscular dystrophies 133
Cross-sectional serum metabolomic study of multiple forms of muscular dystrophy 132
Heart transplantation in a patient with Myotonic Dystrophy type 1 and end-stage dilated cardiomyopathy: A short term follow-up 131
Next generation sequencing applications are ready for genetic diagnosis of muscular dystrophies. 131
Le Distrofie dei Cingoli autosomiche recessive: calpainopatie e disferlinopatie 130
Miocardiopatie e miopatie infiammatorie. 130
Growth hormone deficiency in patients with Duchenne/Becker muscular dystrophy: association with dilated cardiomyopathy 130
Molecular and Muscle Pathology in a series of Caveolinopathy patients 129
Successful combined prenatal diagnosis for Duchenne and facio-scapulo- humeral dystrophies 129
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy 128
Italian validation of INQoL, a quality of life questionnaire for adults with muscle diseases 128
A novel mutation in CPT2 gene in two unrelated patients from Campania region 128
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study 128
Effects of growth hormone therapy in Becker patients with dilated cardiomyopathy 127
Gentamicin administration in Duchenne patients with premature stop codon. Preliminary results 127
Stydy of anti Mullerian hormone levels in patients with myotonic dystrophy type 1. Prelilminary results. 127
[Serum isoenzymes in the diagnosis of some physiopathological conditions in the uterus] 126
The QT dispersion in the risk stratification of sudden death in Becker patients 126
Heart involvement in Emery-Dreifuss muscular dystrophies: new parameters to detect early atrial fibrosis and vulnerability 126
Totale 15.373
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Categoria #
all - tutte 134.923
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 134.923
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.735 0 0 0 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
2025/202616.751 533 673 1.046 886 1.346 9.765 744 382 711 340 217 108
2026/20273.203 181 442 1.331 1.249 0 0 0 0 0 0 0 0
Totale 37.425