Výsledky vyhledávání - "Elena Ordoñez"

Desempeño del profesional contable Laico en el mercado laboral de la Zona 8

Autor: José Edmundo Torres Miranda, Rosa Elena Ordoñez Vivero, David Javier Reyes Andrade

Publikováno v: Yachana Revista Científica; Vol. 6 Núm. 1: Enero-Junio 2017
Revista Universidad Laica Vicente Rocafuerte
Universidad Laica Vicente Rocafuerte
instacron:ULVR
Yachana, Vol 6, Iss 1 (2017)

En la ciudad de Guayaquil en donde funcionan más de 15 universidades, 6 de ellas ofertan la carrera de Contabilidad y Auditoría, de las cuales más del 90% de estos profesionales están destinados a satisfacer la demanda por parte de las empresas d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5b23c0fff44471cae391d2a84c7dd527
http://revistas.ulvr.edu.ec/index.php/yachana/article/view/119

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Screening for Sex Chromosome Aneuploidy by Cell-Free DNA Testing: Patient Choice and Performance

Autor: Ivan Hurtado, Jacques Jani, Elisa Bevilacqua, Laura Rueda, Vincenzo Cirigliano, Elena Ordoñez, Eleonora Mazzone

Publikováno v: Fetal diagnosis and therapy. 44(2)

Objective: To study patient choice regarding testing for sex chromosome aneuploidy (SCA) and the performance of cell-free DNA (cfDNA) screening for SCA. Methods: Patient choice regarding screening for SCA and factors influencing this choice were eval

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25d3d2e3d7ff9cabdd3045aa7641f3e3
https://pubmed.ncbi.nlm.nih.gov/28848190

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Three-Year Follow-Up of a Prenatally Ascertained Apparently Non-Mosaic sSMC(10): Delineation of a Non-Critical Region

Autor: Elisabet Lloveras, Olaya Villa, Nerea Maiz, Laura Barranco, Marta Costa, Alberto Plaja, Cristina Hernando, Vincenzo Cirigliano, Elena Ordoñez

Publikováno v: Cytogenetic and Genome Research. 147:209-211

Small supernumerary marker chromosomes (sSMC) originating from chromosome 10 are rare and usually found in mosaic form. We present a de novo apparently non-mosaic sSMC(10) prenatally diagnosed in amniotic fluid and postnatally confirmed in peripheral

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38855ec0a00f4ecba3f11969c2cf24b6
https://doi.org/10.1159/000444600

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Clinical application of midtrimester non-invasive fetal RHD genotyping and identification of RHD variants in a mixed-ethnic population

Autor: Elena Ordoñez, E. Grau, A. Pericot, J. Cid, I. Teixido, M. Grande, J. L. Marin, Antoni Borrell, Vincenzo Cirigliano

Publikováno v: Prenatal Diagnosis. 33:173-178

Objective This study aims to assess the suitability of non-invasive prenatal RHD genotyping in non-immunized midtrimester pregnant women from a mixed ethnic population, to prevent unnecessary anti-D immunoglobulin prophylaxis and to identify RHD vari

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6ea9ee050590e8c576f61038a8ec3216
https://doi.org/10.1002/pd.4035

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Consideraciones generales de mecanismos técnicos tributarios a los pequeños comerciantes de la Bahía de Guayaquil

Autor: Rosa Elena Ordoñez Vivero, Manuel Tenesaca Gavilánez

Publikováno v: Yachana Revista Científica; Vol. 2 Núm. 1: Julio 2013
Revista Universidad Laica Vicente Rocafuerte
Universidad Laica Vicente Rocafuerte
instacron:ULVR
Yachana, Vol 2, Iss 1 (2016)

Al referimos a la cultura tributaria como un criterio de evaluación técnica financiera del Estado, nos remitimos a las diferentes acciones que se han tomado, ya sea por la naturaleza de los fondos que se recaudan o por el destino específico dentro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::143ed237c73ee04ec1d130d6c13c2fee
http://revistas.ulvr.edu.ec/index.php/yachana/article/view/199

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Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR, results of 9 years of clinical experience

Autor: Carme Fuster, Vincenzo Cirigliano, Elisabet Lloveras, Gianfranco Voglino, Matteo Adinolfi, M. Paz Cañadas, Elena Ordoñez, Antonella Marongiu, Laura Rueda, Maijo Ejarque

Publikováno v: Prenatal Diagnosis. 29:40-49

Background Despite being deliberately targeted to common chromosome aneuploidies, the rapid quantitative fluorescent polymerase chain reaction (QF-PCR) tests can detect the majority of chromosome abnormalities in prenatal diagnosis. The main advantag

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1e84921e375e64194644b14e139758d
https://doi.org/10.1002/pd.2192

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Performance of screening for aneuploidies by cell-free DNA analysis of maternal blood in twin pregnancies

Autor: H. Dierickx, Vincenzo Cirigliano, M. M. Gil, K. H. Nicolaides, Elisa Bevilacqua, Elena Ordoñez, Jacques Jani, P. J. Willems

Objectives To report clinical implementation of cell-free DNA (cfDNA) analysis of maternal blood in screening for trisomies 21, 18 and 13 in twin pregnancies and examine variables that could influence the failure rate of the test. Methods cfDNA testi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cab9704a2ca140e0d1d5a0457bc14a2
http://hdl.handle.net/11573/618605

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Rapid prenatal diagnosis of aneuploidies and zygosity in multiple pregnancies by amniocentesis with single insertion of the needle and quantitative fluorescent PCR

Autor: Vincenzo Cirigliano, Elena Ordoñez, Angeles Sánchez, Paz Cañadas, Carmen Mediano, Inma Farrán, Alberto Plaja

Publikováno v: Prenatal Diagnosis. 23:629-633

Objective To investigate amniotic fluid (AF) samples retrieved in multiple pregnancies by single insertion of the needle, for rapid assessment of chromosome copy number, zygosity, and cross-contamination between fetuses, using Quantitative Fluorescen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e7dcd44f8dae9dc6cc56d5a5f9ca0767
https://doi.org/10.1002/pd.655

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Evaluation of Sample Stability and Automated DNA Extraction for Fetal Sex Determination Using Cell-Free Fetal DNA in Maternal Plasma

Autor: Laura Rueda, Vincenzo Cirigliano, M. Paz Cañadas, Carme Fuster, Elena Ordoñez

Publikováno v: BioMed Research International, Vol 2013 (2013)
BioMed Research International

Objective. The detection of paternally inherited sequences in maternal plasma, such as the SRY gene for fetal sexing or RHD for fetal blood group genotyping, is becoming part of daily routine in diagnostic laboratories. Due to the low percentage of f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f77eee7d56c8d1aa8634672784bc6235
https://doaj.org/article/47eb008886ba4fec9c5a9398d17c788a

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