IRIS
POLITANO, Luisa
 Distribuzione geografica
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Continente #
EU - Europa 6.195
NA - Nord America 5.747
AS - Asia 960
SA - Sud America 14
AF - Africa 12
Continente sconosciuto - Info sul continente non disponibili 8
OC - Oceania 7
Totale 12.943
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Nazione #
US - Stati Uniti d'America 5.718
IE - Irlanda 2.038
UA - Ucraina 1.062
GB - Regno Unito 841
DE - Germania 510
IT - Italia 500
FR - Francia 341
CN - Cina 327
SE - Svezia 314
SG - Singapore 292
FI - Finlandia 282
TR - Turchia 212
GR - Grecia 177
VN - Vietnam 71
BE - Belgio 35
CA - Canada 25
ES - Italia 23
CZ - Repubblica Ceca 17
AT - Austria 15
IN - India 15
KR - Corea 11
EU - Europa 8
ID - Indonesia 8
NL - Olanda 8
BR - Brasile 7
EG - Egitto 6
HK - Hong Kong 6
PT - Portogallo 5
RU - Federazione Russa 5
CH - Svizzera 4
CY - Cipro 4
IS - Islanda 4
MX - Messico 4
NZ - Nuova Zelanda 4
SC - Seychelles 4
AU - Australia 3
CL - Cile 3
JP - Giappone 3
PL - Polonia 3
RO - Romania 3
AE - Emirati Arabi Uniti 2
CO - Colombia 2
HR - Croazia 2
MY - Malesia 2
AL - Albania 1
AR - Argentina 1
BD - Bangladesh 1
BG - Bulgaria 1
DK - Danimarca 1
IL - Israele 1
IR - Iran 1
KZ - Kazakistan 1
LT - Lituania 1
MA - Marocco 1
NG - Nigeria 1
PE - Perù 1
PH - Filippine 1
PK - Pakistan 1
RS - Serbia 1
SM - San Marino 1
TW - Taiwan 1
Totale 12.943
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Città #
Dublin 2.036
Jacksonville 1.647
Chandler 1.008
Princeton 316
Medford 248
Roxbury 195
Ann Arbor 183
Boardman 180
Singapore 176
Wilmington 148
San Mateo 128
Woodbridge 125
Bremen 111
Cambridge 90
Caserta 90
Beijing 81
Dong Ket 66
Des Moines 58
Mountain View 52
Düsseldorf 42
Houston 37
Jinan 34
New York 33
Brussels 27
Ashburn 25
Norwalk 24
Auburn Hills 23
Nanjing 23
Redwood City 22
Helsinki 19
Nanchang 18
Hebei 17
Shenyang 16
Rome 15
Vienna 15
Naples 14
Napoli 14
Haikou 13
Hangzhou 13
Milan 13
Munich 13
Santiago de Compostela 13
Los Angeles 12
West Jordan 12
Zhengzhou 12
Ottawa 11
Taiyuan 11
Tianjin 11
Venice 11
Seoul 10
Taizhou 10
Brno 9
London 9
Trieste 9
Changsha 8
Guangzhou 8
Lanzhou 7
Lappeenranta 7
Ningbo 7
Seattle 7
Barano D'ischia 6
Columbus 6
Grafing 6
Jiaxing 6
Olomouc 6
Avellino 5
Castellammare Di Stabia 5
Halle 5
Pune 5
Tappahannock 5
Venezia 5
Antalya 4
Cedar Knolls 4
Groningen 4
Kocaeli 4
Lubbock 4
Palermo 4
Paterno 4
Québec 4
San Mango 4
Agropoli 3
Andover 3
Bolzano 3
Brescia 3
Castelfidardo 3
Changchun 3
Dearborn 3
Ferrara 3
Gunzenhausen 3
Hanoi 3
Kunming 3
Mahora 3
Marano Di Napoli 3
Miami 3
Oconomowoc 3
Pignataro Maggiore 3
Prato 3
Rubiana 3
Shanghai 3
Acerra 2
Totale 7.747
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Nome #
1) Comparison between SPECT myocardical scintigraphy with 201Tl and 99mTc-MIBI in patients affected by Duchenne's dystrophy 139
1) Study of myocardial perfusion with Tl-201 in patients affected by Duchenne's/Becker's muscolar dystrophy 135
IperCKemia asintomatica. Quando e perchè fare l'indagine genetica 111
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes 81
Cardiomyopathies associated with Muscular Dystrophies 79
Novel small mutations along the DMD/BMD gene associated with different phenotypes 78
A report on 528 intragenic deletions detected in DMD and BMD patients by an Italian collaborative study 72
High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithm 71
Autonomic nervous system imbalance and left ventricular systolic dysfunction as potential candidates for arrhythmogenesis in Becker muscular dystrophy 70
Novel mutations in LMNA A/C gene and associated phenotypes 70
Dispositivo per la valutazione del test del "cammino dei sei minuti (six minutes walking test)" 70
Dispositivo per la valutazione del test del cammino dei 6 minuti 69
The effect of atrial preference pacing on atrial fibrillation electrophysiological substrate in Myotonic Dystrophy type 1 population. 68
Burden, professional support, and social network in families of children and young adults with muscular dystrophies. 66
Right atrial appendage versus Bachmann's bundle stimulation: a two-year comparative study of electrical parameters in myotonic dystrophy type-1 patients. 66
Paroxysmal atrial fibrillation in myotonic dystrophy type 1 patients: P wave duration and dispersion analysis. 65
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. 65
Current therapeutic guidelines in Duchenne Muscular Dystrophy to prolong life. 65
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. 64
Early onset of cardiomyopathy and primary prevention of sudden death in X-linked Emery-Dreifuss muscular dystrophy. 64
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene 64
Italian validation of INQoL, a quality of life questionnaire for adults with muscle diseases 63
SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin function 63
Affinity proteomics within rare diseases: a BIO-NMD study for blood biomarkers of muscular dystrophies 63
Multiple heterozygosity for different muscle genes is not rare among individuals with pauci-symptomatic hyperCKemia 63
Does Bachmann's bundle pacing prevent atrial fibrillation in myotonic dystrophy type 1 patients? A 12 months follow-up study 62
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein 62
Regional and transmural dispersion of repolarisation in patients with Emery-Dreifuss muscular dystrophy. 62
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 61
Le Distrofie dei Cingoli autosomiche recessive: calpainopatie e disferlinopatie 60
Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies 60
Identification of the Syrian hamster cardiomyopathy gene 60
Familial dilated cardiomyopathy associated with the typical dystrophin BMD mutation. Report on two additional cases 60
Right atrial preference pacing algorithm in the prevention of paroxysmal atrial fibrillation in myotonic dystrophy type 1 patients: a long term follow-up study. 59
ACE inhibition to slow progression of myocardial fibrosis in muscular dystrophies 59
"I have got something positive out of this situation": psychological benefits of caregiving in relatives of young people with muscular dystrophy. 58
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy 58
Risk of arrhythmias in MYotonic Dystrophy: trial design of the RAMYD study 58
Struggle for life in lethal muscular diseases ultimate achievement 58
Effects of growth hormone therapy in Becker patients with dilated cardiomyopathy 57
Usefulness of Heart Rate Variability as a predictor of sudden cardiac death in muscular dystrophies 57
Far field R-wave sensing in Myotonic Dystrophy type 1: right atrial appendage versus Bachmann's bundle region lead placement. 57
Evaluation of the cardiomyopathy in Becker muscular dystrophy 57
6 Min walk test 12 month changes in DMD: correlation with the genotype 57
X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sample 56
Does a high percentage of right ventricular pacing influence the incidence of paroxysmal atrial fibrillation in myotonic dystrophy type 1 patients? 56
Dystrophin gene scanning by DHPLC of DMD carriers without deletions or duplications 56
Miocardiopatie e miopatie infiammatorie. 56
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients. 56
Cross-sectional serum metabolomic study of multiple forms of muscular dystrophy 56
Unusual association of Kallmann syndrome with empty sella and arachnoid cyst 55
6 minute walk test in Duchenne MD patients with different mutations: 12 month changes 55
Acta Myologica (myopathies, cardiomyopathies and neuromyopathies) 55
X chromosome inactivation pattern in Duchenne muscular dystrophy carriers 55
Molecular and Muscle Pathology in a series of Caveolinopathy patients 54
Early onset "electrical" heart failure in myotonic dystrophy type 1 patient: the role of ICD biventricular pacing. 54
P dispersion: a new electrocardiographic parameter to evaluate the risk of atrial arrhythmias in Emery-Dreifuss muscular dystrophies 54
Dysferlinopathy presenting as facio-scapulo-humeral dystrophy 54
Corneal endothelium study in patients with myotonic distrophy. 54
Heart transplantation in patients with dystrophinopathic cardiomyopathy: Review of the literature and personal series 54
Successful combined prenatal diagnosis for Duchenne and facio-scapulo- humeral dystrophies 53
A preliminary randomized study of growth hormone administration in Becker and Duchenne muscular dystrophies 53
Next generation sequencing applications are ready for genetic diagnosis of muscular dystrophies. 53
Oral presentation: Treatment of Duchenne dystrophy: results of 7 years cloprednol oral administration 53
Increased heterogeneity of ventricular repolarization in myotonic dystrophy type 1 population 53
Detection of a nonsense mutation in the dystrophin gene by multiple SSCP 52
Evaluation of Becker cardiomyopathy by Vest investigation 52
24 month longitudinal data in ambulant boys with D uchenne muscular dystrophy. 52
Anterior capsule phimosis and capsular block syndrome in a patient with Steinert myotonic dystrophy: A case report 52
P-wave duration and dispersion in patients with Emery-Dreifuss muscular dystrophy. 52
Double carrier status in CANP3 and beta-sarcoglycan genes results in a mild disease phenotype 52
Growth hormone evaluation in patients with dystrophinopathic muscular dystrophy and dilated cardiomyopathy 52
G.O.7 Multiple genetic variations in limb-girdle muscular dystrophies 52
Evaluation of cardiac and respiratory involvement in sarcoglycanopathies 51
Clinical and genetic findings in sarcoglycanopathies 51
Optimal site for atrial lead implantation in myotonic dystrophy patients: the role of Bachmann's Bundle stimulation 51
Advances in basic and clinical research in laminopathies. 51
Assessment of Upper Limb function in DMD patients: Comparison with normative data 51
Growth hormone improves left ventricular loading conditions in Becker Muscular Dystrophy 51
Il trattamento chirurgico delle scoliosi nella Distrofia Muscolare di Duchenne. 50
Are there real benefits to implanting cardiac devices in patients with end-stage dilated dystrophinopathic cardiomyopathy? Review of literature and personal results 50
Prevalence of congenital muscular dystrophy in Italy: A population study. 49
Deflazacort in Duchenne muscular dystrophy: a comparison of two different protocols 49
Gene redundancies in the dystrophin-associated protein complex 49
42nd ENMC Sponsored International Workshop: X-linked Cardiomyopathies 49
A novel homozygous beta-sarcoglycan gene mutation: case description. 49
The QT dispersion in the risk stratification of sudden death in Becker patients 49
Analysis of caveolin-3 (CAV-3) gene in patients with limb-girdle muscular dystrophies and/or isolated hyperCKemia 49
Heart involvement in Emery-Dreifuss muscular dystrophies: new parameters to detect early atrial fibrosis and vulnerability 49
The 6 minute walk test and performance of upper limb in ambulant duchenne muscular dystrophy boys. 48
Left ventricular function and perfusion in Becker's muscular dystrophy 48
Long term natural history data in ambulant boys with duchenne muscular dystrophy: 36-month changes. 48
Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study 48
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease 48
Le conseil genetique dans les dystrophies musculaires: resultats de 10 ans d'approche moleculaire 48
Structural basis of cardiomyopathy in Duchenne/Becker carriers. Endomyocardial biopsy evaluation 47
Une forme méconnue de myopathie. III. Definition et caractères cliniques 47
Intraocular pressure in patients with muscular dystrophies 47
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy. 47
Laminopathies: many diseases, one gene. Report of the first Italian Meeting Course on Laminopathies. 47
Totale 5.888
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Categoria #
all - tutte 56.167
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 56.167
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.441 0 324 74 32 293 47 348 43 128 62 60 30
2020/20212.350 213 5 284 171 397 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
2024/202541 21 20 0 0 0 0 0 0 0 0 0 0
Totale 13.344