Search results for "Mosaici"

showing 10 items of 68 documents

Frammenti di mosaico riportati su calcestruzzo:le interazioni con il supporto e il progetto di conservazione

2010

Settore ING-IND/22 - Scienza E Tecnologia Dei Materialimosaics concrete deterioration Villa del CasaleSettore GEO/05 - Geologia Applicatamosaici romanidegrado materiali costitutivi
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A wavelet-based demosaicking algorithm for embedded applications

2010

This paper presents an alternative to the spatial reconstruction of the sampled color filter array acquired through a digital image sensor. A demosaicking operation has to be applied to the raw image to recover the full-resolution color image. We present a low-complexity demosaicking algorithm processing in the wavelet domain. Produced images are available at the output of the algorithm either in the spatial representation or directly in the wavelet domain for high-level post processing in the latter domain. Results show that the computational complexity has been lowered by a factor of five compared to state of the art demosaicking algorithms.

DemosaicingComputer scienceColor imagebusiness.industryComputingMethodologies_IMAGEPROCESSINGANDCOMPUTERVISIONWavelet transformIterative reconstructionDigital imageWaveletColor filter arrayComputer visionArtificial intelligencebusinessImage resolutionAlgorithm2010 Conference on Design and Architectures for Signal and Image Processing (DASIP)
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Familial ring (18) mosaicism in a 23-year-old young adult with 46,XY,r(18) (::p11→q21::)/46,XY karyotype, intellectual disability, motor retardation …

2010

We report on a 23-year-old man with craniofacial findings of the holoprosencephaly spectrum disorder (microcephaly, hypotelorism, depressed nasal bridge, single median maxillary central incisor), fusion of C2-C3 vertebrae, intellectual disability, and severe sleep apnea. Chromosome analysis of blood lymphocytes showed 75% ring (18) cells and 25% normal cells, karyotype mos 46,XY,r(18)(::p11→q21::)[75]/46,XY[25]. His mother was phenotypically normal except for a double ureter and bifid renal pelvis as in his son. She had a supernumerary ring (18) in 10% of blood lymphocytes, karyotype mos 47,XX,+r(18)(::p11→q21::)[10]/46,XX[90]. Familial ring (18) is a rare cytogenetic abnormality. This is t…

AdultMaleGeneticsMonosomyMicrocephalyMosaicismRing chromosomeMothersAneuploidyKaryotypeAnatomyMotor ActivityBiologymedicine.diseasePhenotypeChromosome 18Intellectual DisabilityKaryotypingGeneticsRing 18medicineHumansFemaleSupernumeraryGenetics (clinical)American Journal of Medical Genetics Part A
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Ammonium phosphate method in preservation of marble artifact

2022

In questo lavoro si studiano gli effetti dell'uso del fosfato di ammonio come consolidante nell'ambito del restauro e del consolidamento di una colonna binata nel lato est del chiostro di Santa Maria La Nova a Monreale, Palermo, Italia This paper studies the effects of using ammonium phosphate as a consolidating agent in the restoration and consolidation of a binata column in the east side of the cloister of Santa Maria La Nova in Monreale, Palermo, Italy

restorationsurface consolidationconsolidamento superficialemosaicirestauroSettore L-ART/01 - Storia Dell'Arte Medievalefosfato di ammoniomosaicammonium phosphateMonreale
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Super-resolution-based magnification of endothelium cells from biomicroscope videos of the cornea

2018

We present a practical, robust, and effective pipeline to compute a high-resolution (HR) image of the corneal endothelium starting from a low-resolution (LR) video sequence obtained with a general purpose slit lamp biomicroscope. An image quality typical of dedicated and more expensive confocal microscopes is achieved via software magnification by exploiting information redundancy in the video sequence. In particular, the HR image is generated from the best LR frames, obtained by identifying the most suitable endothelium video subsequence using a support vector machine-based learning approach, followed by a robust graph-based frame registration. Results on long, real sequences show that the…

Settore ING-INF/05 - Sistemi Di Elaborazione Delle InformazioniImage fusionSettore INF/01 - InformaticaImage qualityComputer sciencebusiness.industryFrame (networking)ComputingMethodologies_IMAGEPROCESSINGANDCOMPUTERVISIONImage registrationMagnificationsuper-resolutionImage segmentationAtomic and Molecular Physics and Opticsslit lamp biomicroscope image enhancementComputer Science ApplicationsSupport vector machinecorneal endotheliumSoftwaremachine learningComputer visionimage mosaicingArtificial intelligenceElectrical and Electronic Engineeringbusiness
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Inheritance and variable expression in Rubinstein-Taybi syndrome.

2010

Familial Rubinstein-Taybi syndrome (RTS) is very rare. Here we report on the 6th and 7th case of inherited RTS. Family 1 presents with incomplete or mild RTS over three generations; a 13-year-old girl (proband 1) with mild but typical facial features and learning disabilities, her very mildly affected mother (proband 2), and the maternal grandmother (proband 3). Family 2 includes three females with classical RTS (probands 4-6) and their father (proband 7) with broad thumbs and halluces. Proband 5 also had a brain tumor (ganglioglioma) at the age of 3 years. In probands 1-3, direct sequencing identified a novel CREBBP missense mutation, c.2728A > G (predicting p.Thr910Ala), that was absent i…

ProbandMaleRiskAdolescentDNA Mutational AnalysisMutation MissenseBiologyVariable ExpressionGenetic HeterogeneityGeneticsmedicineMissense mutationHumansPoint MutationFamilyAlleleGenetics (clinical)GeneticsRubinstein-Taybi SyndromeRubinstein–Taybi syndromeGenetic heterogeneityMosaicismPoint mutationmedicine.diseaseCREB-Binding ProteinPedigreePhenotypeChild PreschoolMutation (genetic algorithm)FemaleAmerican journal of medical genetics. Part A
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Tecsis: Low-Cost Methodology To Distinguish Archaeological Findings

2006

The automatic or semi-automatic research of archaeological findings includes some methodologies and algorithms of the Computer Vision. Reconstruction of a scene is one of the key step to get the solution to that challenge. This paper will address a methodology to reconstruction underwater scenes with mosaicing techniques. The reconstruction of scene will be the video-mosaic of sea bottom landscapes starting from single video frames. The methodology is based on the evaluation of the optic °ow in between frames, and its motion estimation has been evaluated on the extracted features from the common areas of consecutive pairs frames. This approach carried out the motion model from a geometric p…

Motion compensationEcologySettore INF/01 - InformaticaComputer scienceFrame (networking)ComputingMethodologies_IMAGEPROCESSINGANDCOMPUTERVISIONMotion modelArchaeologyGeometrical transformationMotion (physics)Motion estimationKey (cryptography)General Earth and Planetary SciencesArchaeological findingNoise (video)MosaicingProjection (set theory)Ecology Evolution Behavior and SystematicsComputingMethodologies_COMPUTERGRAPHICSGeneral Environmental ScienceReference frame
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Clinical application of embryo aneuploidy testing by next-generation sequencing

2019

Abstract We review here the evolution in the field of embryo aneuploidy testing over the last 20 years, from the analysis of a subset of chromosomes by fluorescence in situ hybridisation to the transition toward a more comprehensive analysis of all 24 chromosomes. This current comprehensive aneuploidy testing most commonly employs next-generation sequencing (NGS). We present our experience in over 130 000 embryo biopsies using this technology. The incidence of aneuploidy was lower in trophectoderm biopsies compared to cleavage-stage biopsies. We also confirmed by NGS that embryo aneuploidy rates increased with increasing maternal age, mostly attributable to an increase in complex aneuploid …

Male0301 basic medicineTime FactorsNoninvasive Prenatal TestingAneuploidySingle Embryo TransferBiologyMiscarriageAndrology03 medical and health sciences0302 clinical medicinePregnancyRisk FactorsRecurrent miscarriagemedicineHumansGenetic TestingBlastocystPrecision MedicinePreimplantation DiagnosisGenetic testingPregnancy030219 obstetrics & reproductive medicinemedicine.diagnostic_testMosaicismHigh-Throughput Nucleotide SequencingCell BiologyGeneral MedicineAneuploidyEmbryo Transfermedicine.diseaseEmbryo transferBlastocyst030104 developmental biologymedicine.anatomical_structureReproductive MedicineCytogenetic AnalysisFemaleCell-Free Nucleic AcidsBiology of Reproduction
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Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome.

2022

Funder: Università degli Studi di Catania

BUB1B gene Epileptic seizure Microcephaly Mosaic variegated aneuploidy 1 (MVA1) syndrome Ovary cystMosaicismCell Cycle ProteinsOvary cystDermatologyGeneral MedicineSyndromeBUB1B geneProtein Serine-Threonine KinasesAneuploidyPsychiatry and Mental healthSeizuresMosaic variegated aneuploidy 1 (MVA1) syndromeMutationEpileptic seizureMicrocephalyHumansNeurology (clinical)Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
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[Y chromosome in Turner syndrome].

2017

Turner syndrome (TS) is an inherited genetic disorder caused by numerical and/or structural chromosome X aberrations occurring at a frequency of 1:1200-1:2500 live-born girls. The most common karyotype is X chromosome monosomy (45,X) (approximately 50-60% of cases). Approximately 5-6% of patients may have abnormal Y chromosome or mosaicism characterized by the coexistence of 45,X cell line with cell line in which all or part of chromosome Y is present. In patients with TS who have all or fragmented genetic material from chromosome Y there is a substantial risk of cancerous lesions in these dysgenetic gonads. This paper stands for the review of the current knowledge on the genetic material o…

GeneticsOvarian NeoplasmsMonosomyChromosomes Human Ybusiness.industryMosaicismGenetic disorderGonadoblastomaChromosomeTurner SyndromeKaryotypeGeneral Medicinemedicine.diseaseY chromosomeTurner syndromeMutationmedicineHumansFemaleGonadoblastomabusinessX chromosomePediatric endocrinology, diabetes, and metabolism
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