POLITANO, Luisa
 Distribuzione geografica
Continente #
EU - Europa 6.154
NA - Nord America 5.725
AS - Asia 647
SA - Sud America 14
AF - Africa 12
Continente sconosciuto - Info sul continente non disponibili 8
OC - Oceania 7
Totale 12.567
Nazione #
US - Stati Uniti d'America 5.696
IE - Irlanda 2.038
UA - Ucraina 1.062
GB - Regno Unito 839
DE - Germania 500
IT - Italia 492
FR - Francia 338
CN - Cina 315
SE - Svezia 314
FI - Finlandia 278
TR - Turchia 212
GR - Grecia 177
VN - Vietnam 69
BE - Belgio 35
CA - Canada 25
ES - Italia 23
AT - Austria 15
IN - India 13
EU - Europa 8
ID - Indonesia 8
NL - Olanda 8
BR - Brasile 7
EG - Egitto 6
HK - Hong Kong 6
CZ - Repubblica Ceca 5
PT - Portogallo 5
SG - Singapore 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
RU - Federazione Russa 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
KR - Corea 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 12.567
Città #
Dublin 2.036
Jacksonville 1.647
Chandler 1.008
Princeton 316
Medford 248
Roxbury 195
Ann Arbor 183
Boardman 172
Wilmington 148
San Mateo 128
Woodbridge 125
Bremen 111
Cambridge 90
Caserta 90
Beijing 78
Dong Ket 66
Des Moines 58
Mountain View 52
Düsseldorf 42
Houston 37
Jinan 34
New York 33
Brussels 27
Ashburn 24
Norwalk 24
Auburn Hills 23
Nanjing 23
Redwood City 22
Nanchang 18
Hebei 17
Helsinki 17
Shenyang 16
Vienna 15
Napoli 14
Haikou 13
Hangzhou 13
Milan 13
Rome 13
Santiago de Compostela 13
Naples 12
West Jordan 12
Zhengzhou 12
Ottawa 11
Taiyuan 11
Tianjin 11
Venice 11
Taizhou 10
London 9
Trieste 9
Changsha 8
Guangzhou 8
Lanzhou 7
Ningbo 7
Seattle 7
Barano D'ischia 6
Columbus 6
Grafing 6
Jiaxing 6
Los Angeles 6
Avellino 5
Castellammare Di Stabia 5
Halle 5
Lappeenranta 5
Munich 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
Brno 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
Auckland 2
Brookings 2
Cagliari 2
Totale 7.521
Nome #
1) Comparison between SPECT myocardical scintigraphy with 201Tl and 99mTc-MIBI in patients affected by Duchenne's dystrophy 129
1) Study of myocardial perfusion with Tl-201 in patients affected by Duchenne's/Becker's muscolar dystrophy 126
IperCKemia asintomatica. Quando e perchè fare l'indagine genetica 110
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes 80
Novel small mutations along the DMD/BMD gene associated with different phenotypes 77
Cardiomyopathies associated with Muscular Dystrophies 73
A report on 528 intragenic deletions detected in DMD and BMD patients by an Italian collaborative study 70
Novel mutations in LMNA A/C gene and associated phenotypes 69
Autonomic nervous system imbalance and left ventricular systolic dysfunction as potential candidates for arrhythmogenesis in Becker muscular dystrophy 68
Dispositivo per la valutazione del test del "cammino dei sei minuti (six minutes walking test)" 68
High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithm 67
The effect of atrial preference pacing on atrial fibrillation electrophysiological substrate in Myotonic Dystrophy type 1 population. 67
Dispositivo per la valutazione del test del cammino dei 6 minuti 67
Burden, professional support, and social network in families of children and young adults with muscular dystrophies. 65
Paroxysmal atrial fibrillation in myotonic dystrophy type 1 patients: P wave duration and dispersion analysis. 65
Right atrial appendage versus Bachmann's bundle stimulation: a two-year comparative study of electrical parameters in myotonic dystrophy type-1 patients. 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. 64
Early onset of cardiomyopathy and primary prevention of sudden death in X-linked Emery-Dreifuss muscular dystrophy. 64
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. 63
Affinity proteomics within rare diseases: a BIO-NMD study for blood biomarkers of muscular dystrophies 63
Current therapeutic guidelines in Duchenne Muscular Dystrophy to prolong life. 63
Multiple heterozygosity for different muscle genes is not rare among individuals with pauci-symptomatic hyperCKemia 63
Italian validation of INQoL, a quality of life questionnaire for adults with muscle diseases 62
SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin function 62
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene 62
Does Bachmann's bundle pacing prevent atrial fibrillation in myotonic dystrophy type 1 patients? A 12 months follow-up study 61
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein 61
Regional and transmural dispersion of repolarisation in patients with Emery-Dreifuss muscular dystrophy. 61
Le Distrofie dei Cingoli autosomiche recessive: calpainopatie e disferlinopatie 60
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 60
Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies 59
Identification of the Syrian hamster cardiomyopathy gene 59
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy 58
Right atrial preference pacing algorithm in the prevention of paroxysmal atrial fibrillation in myotonic dystrophy type 1 patients: a long term follow-up study. 58
Familial dilated cardiomyopathy associated with the typical dystrophin BMD mutation. Report on two additional cases 58
Risk of arrhythmias in MYotonic Dystrophy: trial design of the RAMYD study 57
Struggle for life in lethal muscular diseases ultimate achievement 57
6 Min walk test 12 month changes in DMD: correlation with the genotype 57
ACE inhibition to slow progression of myocardial fibrosis in muscular dystrophies 57
"I have got something positive out of this situation": psychological benefits of caregiving in relatives of young people with muscular dystrophy. 56
Effects of growth hormone therapy in Becker patients with dilated cardiomyopathy 56
X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sample 56
Usefulness of Heart Rate Variability as a predictor of sudden cardiac death in muscular dystrophies 56
Far field R-wave sensing in Myotonic Dystrophy type 1: right atrial appendage versus Bachmann's bundle region lead placement. 56
Evaluation of the cardiomyopathy in Becker muscular dystrophy 56
Unusual association of Kallmann syndrome with empty sella and arachnoid cyst 55
Does a high percentage of right ventricular pacing influence the incidence of paroxysmal atrial fibrillation in myotonic dystrophy type 1 patients? 55
Dystrophin gene scanning by DHPLC of DMD carriers without deletions or duplications 55
Miocardiopatie e miopatie infiammatorie. 55
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients. 55
Cross-sectional serum metabolomic study of multiple forms of muscular dystrophy 55
Molecular and Muscle Pathology in a series of Caveolinopathy patients 54
Acta Myologica (myopathies, cardiomyopathies and neuromyopathies) 54
X chromosome inactivation pattern in Duchenne muscular dystrophy carriers 54
Early onset "electrical" heart failure in myotonic dystrophy type 1 patient: the role of ICD biventricular pacing. 53
Successful combined prenatal diagnosis for Duchenne and facio-scapulo- humeral dystrophies 53
6 minute walk test in Duchenne MD patients with different mutations: 12 month changes 53
P dispersion: a new electrocardiographic parameter to evaluate the risk of atrial arrhythmias in Emery-Dreifuss muscular dystrophies 53
Dysferlinopathy presenting as facio-scapulo-humeral dystrophy 53
Corneal endothelium study in patients with myotonic distrophy. 53
Heart transplantation in patients with dystrophinopathic cardiomyopathy: Review of the literature and personal series 53
Detection of a nonsense mutation in the dystrophin gene by multiple SSCP 52
Anterior capsule phimosis and capsular block syndrome in a patient with Steinert myotonic dystrophy: A case report 52
A preliminary randomized study of growth hormone administration in Becker and Duchenne muscular dystrophies 52
Next generation sequencing applications are ready for genetic diagnosis of muscular dystrophies. 52
G.O.7 Multiple genetic variations in limb-girdle muscular dystrophies 52
Increased heterogeneity of ventricular repolarization in myotonic dystrophy type 1 population 52
Evaluation of cardiac and respiratory involvement in sarcoglycanopathies 51
Evaluation of Becker cardiomyopathy by Vest investigation 51
24 month longitudinal data in ambulant boys with D uchenne muscular dystrophy. 51
P-wave duration and dispersion in patients with Emery-Dreifuss muscular dystrophy. 51
Double carrier status in CANP3 and beta-sarcoglycan genes results in a mild disease phenotype 51
Assessment of Upper Limb function in DMD patients: Comparison with normative data 51
Oral presentation: Treatment of Duchenne dystrophy: results of 7 years cloprednol oral administration 51
Growth hormone evaluation in patients with dystrophinopathic muscular dystrophy and dilated cardiomyopathy 51
Clinical and genetic findings in sarcoglycanopathies 50
Optimal site for atrial lead implantation in myotonic dystrophy patients: the role of Bachmann's Bundle stimulation 50
Advances in basic and clinical research in laminopathies. 50
Growth hormone improves left ventricular loading conditions in Becker Muscular Dystrophy 50
Il trattamento chirurgico delle scoliosi nella Distrofia Muscolare di Duchenne. 49
Prevalence of congenital muscular dystrophy in Italy: A population study. 48
Deflazacort in Duchenne muscular dystrophy: a comparison of two different protocols 48
Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study 48
Gene redundancies in the dystrophin-associated protein complex 48
Le conseil genetique dans les dystrophies musculaires: resultats de 10 ans d'approche moleculaire 48
Heart involvement in Emery-Dreifuss muscular dystrophies: new parameters to detect early atrial fibrosis and vulnerability 48
The 6 minute walk test and performance of upper limb in ambulant duchenne muscular dystrophy boys. 47
Left ventricular function and perfusion in Becker's muscular dystrophy 47
Structural basis of cardiomyopathy in Duchenne/Becker carriers. Endomyocardial biopsy evaluation 47
Long term natural history data in ambulant boys with duchenne muscular dystrophy: 36-month changes. 47
Intraocular pressure in patients with muscular dystrophies 47
Laminopathies: many diseases, one gene. Report of the first Italian Meeting Course on Laminopathies. 47
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease 47
Une forme méconnue de myopathie. III. Definition et caractères cliniques 46
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy. 46
Risk of arrhythmia in type I Myotonic Dystrophy: the role of clinical and genetic variables 46
Is the value of QT dispersion a valid method to foresee the risk of sudden death? A study in Becker patients 46
42nd ENMC Sponsored International Workshop: X-linked Cardiomyopathies 46
The QT dispersion in the risk stratification of sudden death in Becker patients 46
LA SINDROME DI KALLMANN: INSOLITA ASSOCIAZIONE LESIONALE. 46
Totale 5.762
Categoria #
all - tutte 47.117
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 47.117


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201952 0 0 0 0 0 0 0 0 0 12 11 29
2019/20201.805 364 324 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
2023/2024997 114 59 60 128 526 51 13 25 8 13 0 0
Totale 12.968