POLITANO, Luisa
 Distribuzione geografica
Continente #
EU - Europa 125
AS - Asia 48
NA - Nord America 27
AF - Africa 1
Totale 201
Nazione #
IT - Italia 59
IE - Irlanda 35
VN - Vietnam 30
US - Stati Uniti d'America 24
GB - Regno Unito 8
JP - Giappone 8
RU - Federazione Russa 6
FR - Francia 5
NL - Olanda 4
CA - Canada 3
CN - Cina 3
IN - India 3
GR - Grecia 2
IR - Iran 2
SE - Svezia 2
AE - Emirati Arabi Uniti 1
CZ - Repubblica Ceca 1
FI - Finlandia 1
HK - Hong Kong 1
IS - Islanda 1
PT - Portogallo 1
ZA - Sudafrica 1
Totale 201
Città #
Dublin 35
Caserta 33
Dong Ket 30
Chicago 6
Tokyo 4
Ann Arbor 3
Foggia 3
Grenoble 3
Houston 3
Beijing 2
Boardman 2
Bonnybridge 2
Council Bluffs 2
London 2
Maastricht 2
Moscow 2
Naples 2
Stockholm 2
Acerra 1
Ashburn 1
Assisi 1
Aversa 1
Brampton 1
Calvizzano 1
Cape Town 1
Central 1
Chennai 1
Cheyenne 1
Coimbatore 1
Doncaster 1
Falkirk 1
Groningen 1
Helsinki 1
Hyderabad 1
Kizugawa-shi 1
Kladno 1
Kyoto 1
Messina 1
Milton Keynes 1
Montréal 1
Napoli 1
Olevano Sul Tusciano 1
Osaka 1
Ottawa 1
Padova 1
Paris 1
Redmond 1
Reykjavik 1
Rockville 1
Shiraz 1
South Bend 1
Thessaloniki 1
Thessaloníki 1
Valence 1
Wilmington 1
Wuhan 1
Totale 176
Nome #
Heart transplantation in patients with dystrophinopathic cardiomyopathy: Review of the literature and personal series, file dfd1c04b-de05-0799-e053-6605fe0a8ddb 38
Cross-sectional serum metabolomic study of multiple forms of muscular dystrophy, file dfd1c04b-d800-0799-e053-6605fe0a8ddb 34
Bachmann bundle pacing reduces atrial electromechanical delay in type 1 myotonic dystrophy patients, file dfd1c04b-fbaf-0799-e053-6605fe0a8ddb 30
Idebenone reduces respiratory complications in patients with Duchenne muscular dystrophy, file dfd1c04b-5f17-0799-e053-6605fe0a8ddb 18
TMEM5-associated dystroglycanopathy presenting with CMD and mild limb-girdle muscle involvement, file dfd1c04b-614c-0799-e053-6605fe0a8ddb 15
Galactose-1-phosphate uridyltransferase deficiency: A literature review of the putative mechanisms of short and long-term complications and allelic variants, file dfd1c04b-d8cb-0799-e053-6605fe0a8ddb 11
Longitudinal effect of eteplirsen versus historical control on ambulation in Duchenne muscular dystrophy, file dfd1c04b-5c61-0799-e053-6605fe0a8ddb 7
Genetic modifiers of duchenne muscular dystrophy and dilated cardiomyopathy, file dfd1c04b-e2d1-0799-e053-6605fe0a8ddb 6
Gentamicin administration in Duchenne patients with premature stop codon. Preliminary results, file dfd1c04a-4beb-0799-e053-6605fe0a8ddb 4
Determining the role of skewed X-chromosome inactivation in developing muscle symptoms in carriers of Duchenne muscular dystrophy., file dfd1c04b-5d1c-0799-e053-6605fe0a8ddb 4
Evaluation of cardiac and respiratory involvement in sarcoglycanopathies, file dfd1c04a-868d-0799-e053-6605fe0a8ddb 3
Categorizing natural history trajectories of ambulatory function measured by the 6-minute walk distance in patients with Duchenne muscular dystrophy, file dfd1c04b-5f15-0799-e053-6605fe0a8ddb 3
Copy Number Variants Account for a Tiny Fraction of Undiagnosed Myopathic Patients, file dfd1c04c-319b-0799-e053-6605fe0a8ddb 3
Affinity proteomics within rare diseases: a BIO-NMD study for blood biomarkers of muscular dystrophies, file dfd1c04a-4b6e-0799-e053-6605fe0a8ddb 2
Comparison of X chromosome inactivation in Duchenne muscle/myocardium manifesting carriers, non manifesting carriers and related daughters, file dfd1c04a-4ce6-0799-e053-6605fe0a8ddb 2
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy., file dfd1c04a-5304-0799-e053-6605fe0a8ddb 2
DMD Phenotype in Girls with a de novo Balanced X;3 Autosome Translocation: A Case Report, file dfd1c04a-5aa7-0799-e053-6605fe0a8ddb 2
Increased dispersion of ventricular repolarization in emery dreifuss muscular dystrophy patient, file dfd1c04a-3426-0799-e053-6605fe0a8ddb 1
Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies, file dfd1c04a-3b07-0799-e053-6605fe0a8ddb 1
Intraocular pressure in patients with muscular dystrophies, file dfd1c04a-447c-0799-e053-6605fe0a8ddb 1
Le Distrofie dei Cingoli autosomiche recessive: calpainopatie e disferlinopatie, file dfd1c04a-47a1-0799-e053-6605fe0a8ddb 1
Regional and transmural dispersion of repolarisation in patients with Emery-Dreifuss muscular dystrophy., file dfd1c04a-4827-0799-e053-6605fe0a8ddb 1
Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study, file dfd1c04a-4c72-0799-e053-6605fe0a8ddb 1
Burden, professional support, and social network in families of children and young adults with muscular dystrophies., file dfd1c04a-4f32-0799-e053-6605fe0a8ddb 1
Structural basis of cardiomyopathy in Duchenne/Becker carriers. Endomyocardial biopsy evaluation, file dfd1c04a-5282-0799-e053-6605fe0a8ddb 1
Motor Chip: a Comparative Genomic Hybridization Microarray for Copy-Number Mutations in 245 Neuromuscular Disorders, file dfd1c04a-5417-0799-e053-6605fe0a8ddb 1
Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations, file dfd1c04a-5ba9-0799-e053-6605fe0a8ddb 1
The effect of atrial preference pacing on atrial fibrillation electrophysiological substrate in Myotonic Dystrophy type 1 population., file dfd1c04a-5ec8-0799-e053-6605fe0a8ddb 1
Early onset of cardiomyopathy and primary prevention of sudden death in X-linked Emery-Dreifuss muscular dystrophy., file dfd1c04a-8d14-0799-e053-6605fe0a8ddb 1
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., file dfd1c04a-a40b-0799-e053-6605fe0a8ddb 1
Does a high percentage of right ventricular pacing influence the incidence of paroxysmal atrial fibrillation in myotonic dystrophy type 1 patients?, file dfd1c04a-a46c-0799-e053-6605fe0a8ddb 1
The NorthStar Ambulatory Assessment in Duchenne muscular dystrophy: Considerations for the design of clinical trials, file dfd1c04b-6322-0799-e053-6605fe0a8ddb 1
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients., file dfd1c04b-8a27-0799-e053-6605fe0a8ddb 1
Skewed X-chromosome inactivation plays a crucial role in the onset of symptoms in carriers of Becker muscular dystrophy., file dfd1c04b-d81b-0799-e053-6605fe0a8ddb 1
Clarification on Uveal Melanoma Associated With Myotonic Dystrophy, file dfd1c04c-2c3a-0799-e053-6605fe0a8ddb 1
Elevated TGF β2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes, file dfd1c04c-39c4-0799-e053-6605fe0a8ddb 1
Health-related quality of life and functional changes in DMD: A 12-month longitudinal cohort study, file dfd1c04c-7b42-0799-e053-6605fe0a8ddb 1
Are there real benefits to implanting cardiac devices in patients with end-stage dilated dystrophinopathic cardiomyopathy? Review of literature and personal results, file dfd1c04c-ca1b-0799-e053-6605fe0a8ddb 1
Study of expression of genes potentially responsible for reduced fitness in patients with myotonic dystrophy type 1 and identification of new biomarkers of testicular function, file dfd1c04c-cb65-0799-e053-6605fe0a8ddb 1
Totale 206
Categoria #
all - tutte 1.027
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 1.027


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202014 0 0 0 2 1 0 1 1 2 5 2 0
2020/202156 1 1 6 2 3 4 5 1 0 1 1 31
2021/20228 0 1 0 0 1 1 1 0 0 1 3 0
2022/202369 0 1 0 4 1 2 3 5 43 7 3 0
2023/202427 0 1 2 3 4 5 4 3 2 3 0 0
Totale 206