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Institution

Casa Sollievo della Sofferenza

HealthcareSan Giovanni Rotondo, Italy
About: Casa Sollievo della Sofferenza is a healthcare organization based out in San Giovanni Rotondo, Italy. It is known for research contribution in the topics: Population & Cancer. The organization has 2234 authors who have published 6183 publications receiving 239811 citations. The organization is also known as: Home for Relief of the Suffering.


Papers
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Journal Article
TL;DR: White-matter volume loss may precede gray-matter atrophy and may be associated with neuronal dysfunction in early disease in Huntington's disease.
Abstract: We studied the anatomic and functional changes in various brain areas during the course of Huntington9s disease (HD) in a large cohort of mutation-positive individuals (n = 71) encompassing the complete range of disability (presymptomatic through stage V), and in healthy controls, for the purpose of defining both degenerative and dysfunctional brain changes in the same subjects. Methods: We used an MRI and unsupervised multiparametric segmentation procedure based on a relaxometric approach to measure in vivo brain volumes in 71 subjects with presymptomatic to advanced HD. The same population was evaluated by 18F-FDG PET to assess variations in brain glucose metabolism. To predict age at onset in unaffected mutation carriers, we considered the estimated number of years from each subject9s age to manifested HD symptoms, for a given expanded triplet number. Results: Age-adjusted analyses confirmed that the 71 subjects as a group, as well as the subgroup of 24 unaffected presymptomatic subjects at risk for HD, had significantly smaller gray-matter and white-matter volumes and larger cerebrospinal fluid volumes than did controls (P

284 citations

Journal ArticleDOI
TL;DR: The addition of weekly cisplatin to gemcitabine failed to demonstrate any improvement as first-line treatment of advanced pancreatic cancer and combined therapy produced more hematologic toxicity, without relevant differences in nonhematologic toxicity.
Abstract: Purpose Single-agent gemcitabine became standard first-line treatment for advanced pancreatic cancer after demonstration of superiority compared with fluorouracil. The Gruppo Italiano Pancreas 1 randomized phase III trial aimed to compare gemcitabine plus cisplatin versus gemcitabine alone (ClinicalTrials.gov ID NCT00813696). Patients and Methods Patients with locally advanced or metastatic pancreatic cancer, age 18 to 75 years, and Karnofsky performance status (KPS) ≥ 50, were randomly assigned to receive gemcitabine (arm A) or gemcitabine plus cisplatin (arm B). Arm A: gemcitabine 1,000 mg/m2 weekly for 7 weeks, and, after a 1-week rest, on days 1, 8, and 15 every 4 weeks. Arm B: cisplatin 25 mg/m2 added weekly to gemcitabine, except cycle 1 day 22. Primary end point was overall survival. To have 8% power of detecting a 0.74 hazard ratio (HR) of death, with bilateral α .05, 355 events were needed and 400 patients planned. Results Four hundred patients were enrolled (arm A: 199; arm B: 201). Median age w...

283 citations

Journal ArticleDOI
Dan E. Arking1, Sara L. Pulit2, Sara L. Pulit3, Sara L. Pulit4  +257 moreInstitutions (73)
TL;DR: In this paper, the authors identified 35 common variant loci associated with QT interval that collectively explain ∼8-10% of QT-interval variation and highlight the importance of calcium regulation in myocardial repolarization.
Abstract: The QT interval, an electrocardiographic measure reflecting myocardial repolarization, is a heritable trait. QT prolongation is a risk factor for ventricular arrhythmias and sudden cardiac death (SCD) and could indicate the presence of the potentially lethal mendelian long-QT syndrome (LQTS). Using a genome-wide association and replication study in up to 100,000 individuals, we identified 35 common variant loci associated with QT interval that collectively explain ∼8-10% of QT-interval variation and highlight the importance of calcium regulation in myocardial repolarization. Rare variant analysis of 6 new QT interval-associated loci in 298 unrelated probands with LQTS identified coding variants not found in controls but of uncertain causality and therefore requiring validation. Several newly identified loci encode proteins that physically interact with other recognized repolarization proteins. Our integration of common variant association, expression and orthogonal protein-protein interaction screens provides new insights into cardiac electrophysiology and identifies new candidate genes for ventricular arrhythmias, LQTS and SCD.

283 citations

Journal ArticleDOI
TL;DR: This novel ultrasound ablation system can successfully isolate multiple pulmonary veins and seems to be effective in preventing recurrent atrial fibrillation in a significant number of patients.
Abstract: Background—Standard mapping and ablation of focal sources of atrial fibrillation are associated with very long procedure times and low efficacy An anatomic approach to complete pulmonary vein isolation could overcome these limitations Methods and Results—Fifteen patients with atrial fibrillation refractory to medication underwent circumferential isolation of the pulmonary veins by using a novel catheter, with an ultrasound transducer (8-MHz) mounted near the tip, in a saline-filled balloon Twelve atrial foci and/or atrial fibrillation triggers were identified in 9 patients (pulmonary vein locations: left upper, 3; right upper, 6; right middle, 1; right lower, 1; and left inferior, 1) In 5 patients, lesions were placed in the absence of any mapped triggers Irrespective of trigger mapping, circumferential isolation of both upper pulmonary veins was attempted in all patients The lower pulmonary veins were ablated when sinus rhythm activation mapping revealed evidence of a sleeve of atrial muscle in the

282 citations


Authors

Showing all 2237 results

NameH-indexPapersCitations
Ralph B. D'Agostino2261287229636
Cisca Wijmenga13666886572
Massimo Mangino11636984902
Xavier Estivill11067359568
Andrea Natale10694552520
Stefano Pileri10063543369
Bruno Dallapiccola9493543208
Fortunato Ciardiello9469547352
F. Bianchi91137040011
Paolo Gasparini9143136059
Joseph G. Gleeson8630723345
Mario Rizzetto7947033693
Giuseppe Leone7465421451
Maurizio Pompili7478320649
Massimo Rugge7459425624
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20233
20229
2021457
2020446
2019409
2018348