Výsledky vyhledávání - "Teresa, Aravena"

Akademický článek

Expansión de la oferta y matrícula de Programas de Magíster en universidades chilenas: una mirada desde las políticas de aseguramiento de la calidad

Autor: María Teresa Aravena Rodríguez, Alexis Meza Sánchez

Publikováno v: Pensamiento Educativo: Revista de Investigación Educacional Latinoamericana, Vol 54, Iss 1, Pp 1-21 (2017)

La oferta y matrícula de programas de magíster ha tenido un crecimiento significativo en los últimos años. Este crecimiento se ha concentrado preferentemente en algunas áreas de conocimiento y en universidades privadas creadas con posterioridad

Externí odkaz: https://doaj.org/article/c0d81372b42c45f1bdef08621df0e0c9

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Akademický článek

VEGFA polymorphisms and cardiovascular anomalies in 22q11 microdeletion syndrome: a case-control and family-based study

Autor: JUAN FRANCISCO CALDERÓN, ALONSO R PUGA, M. LUISA GUZMÁN, CARMEN PAZ ASTETE, MARTA ARRIAZA, MARIANA ARACENA, TERESA ARAVENA, PATRICIA SANZ, GABRIELA M REPETTO

Publikováno v: Biological Research, Vol 42, Iss 4, Pp 461-468 (2009)

Microdeletion 22q11 in humans causes velocardiofacial and DiGeorge syndromes. Most patients share a common 3Mb deletion, but the clinical manifestations are very heterogeneous. Congenital heart disease is present in 50-80% of patients and is a signif

Externí odkaz: https://doaj.org/article/1434e2b2f32b43bb996772f9d9dc75ef

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Turner syndrome in diverse populations

Autor: Joanna Y.L. Tung, Katta M. Girisha, Paul Kruszka, Nicole Fleischer, Engy A. Ashaat, E.V. Badoe, Dalia Farouk Hussen, Neer Shoba Chitrakar, Angélica Moresco, Neveen A. Ashaat, Olufemi Fasanmade, Siddaramappa J. Patil, Mona O. El Ruby, André Mégarbané, Johnathan Watts, Karen Fieggen, Gary T. K. Mok, Dhanya Yesodharan, Milagros M. Dueñas-Roque, Ezana Lulseged, Cedrik Tekendo-Ngongang, Sarah Savage, Saumya Shekhar Jamuar, Vajira H. W. Dissanayake, Nirmala D. Sirisena, Sultana M.H. Faradz, Antonio Richieri-Costa, Kelly L. Jones, Jasmine Chew Yin Goh, Brenda C. Iriele, María Beatriz de Herreros, Brian H.Y. Chung, Godfrey Mutashambara Rwegerera, María Gabriela Obregon, Yonit A. Addissie, Nydia Rena Benita Sihombing, Teresa Aravena, Shubha R. Phadke, Victoria Huckstadt, C. Sampath Paththinige, Meow-Keong Thong, Neerja Gupta, Agustini Utari, Sheela Nampoothiri, Elizabeth Eberechi Oyenusi, Ekanem N. Ekure, Maximilian Muenke, Rupesh Mishra, Oluwarotimi Bolaji Olopade, Annette Uwineza, Vorasuk Shotelersuk, Ambroise Wonkam

Publikováno v: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Am J Med Genet A

Turner syndrome (TS) is a common multiple congenital anomaly syndrome resulting from complete or partial absence of the second X chromosome. TS presents with short stature, infertility secondary to ovarian dysgenesis, cardiac and renal anomalies, cha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf516dfd88789c7ce7186e90a9e30000

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A Deletion of More than 800 kb Is the Most Recurrent Mutation in Chilean Patients with SHOX Gene Defects

Autor: Marcela Lagos, Andreina Cattani, Reyes L, Alejandro Martinez-Aguayo, Arriaza M, Hernan Garcia, Mariana Aracena, Cecilia Mellado, Vera A, H Rumié, Lacourt P, Teresa Aravena, Helena Poggi, Avalos C, Mericq, Godoy C

Publikováno v: Hormone Research in Paediatrics. 84:254-257

Background: Deletions in the SHOX gene are the most frequent genetic cause of Leri-Weill syndrome and Langer mesomelic dysplasia, which are also present in idiopathic short stature. Aim: To describe the molecular and clinical findings observed in 23

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ef4e036fc58c16da63d0f790a76b2b8f
https://doi.org/10.1159/000439109

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Expansión de la oferta y matrícula de Programas de Magíster en universidades chilenas: una mirada desde las políticas de aseguramiento de la calidad

Autor: Alexis Meza Sánchez, María Teresa Aravena Rodríguez

Publikováno v: Pensamiento Educativo: Revista de Investigación Educacional Latinoamericana. 54

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::15d6e63efd52cc1e64db38c17623f64a
https://doi.org/10.7764/pel.54.1.2017.4

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[Congenital anomalies of poor prognosis. Genetics Consensus Committee]

Autor: Rosa A, Pardo Vargas, Mariana, Aracena, Teresa, Aravena, Carolina, Cares, Fanny, Cortés, Víctor, Faundes, Cecilia, Mellado, Cristóbal, Passalacqua, Patricia, Sanz, Silvia, Castillo Taucher

Publikováno v: Revista chilena de pediatria. 87(5)

The Genetic Branch of the Chilean Society of Paediatrics, given the draft Law governing the decriminalisation of abortion on three grounds, focusing on the second ground, which considers the "embryo or foetus suffering from a congenital structural an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5532027837e46539ae5ad3d696311597
https://pubmed.ncbi.nlm.nih.gov/27234469

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Two sisters resembling Gorlin-Chaudhry-Moss syndrome

Autor: Cristóbal Passalacqua, Oscar Pizarro, Teresa Aravena, Mariana Aracena

Publikováno v: American Journal of Medical Genetics Part A. 155:2552-2555

The Gorlin-Chaudhry-Moss syndrome (GCMS), was describe initially by Gorlin et al. [Gorlin et al. (1960)] in two sisters with craniosynostosis, hypertrichosis, hypoplastic labia majora, dental defects, eye anomalies, patent ductus arteriosus, and norm

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f45d522e91ee18b689911a46daf43371
https://doi.org/10.1002/ajmg.a.34204

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Cáncer hereditario de colon: Aportes del diagnóstico genético molecular

Autor: Teresa Aravena, Cristóbal Passalacqua, Silvia Castillo Taucher

Publikováno v: Revista médica de Chile. 138:1530-1534

Background About 30% of cases of colon cancer (CC) have a family history of CC, and only 5% are hereditary forms. Hereditary forms have an increased risk of CC and other tumors. Aim To report the molecular and genetic study in two families with hered

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fa8ec8bef389be2942611c9de65b2f20
https://doi.org/10.4067/s0034-98872010001300009

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ADHD children outperform normal children in an artificial grammar implicit learning task: ERP and RT evidence

Autor: Esteban Hurtado, Francisco Ceric, Ricardo Rosas, Marcela Tenorio, María Teresa Aravena, Catalina Mourgues, Carolina Thibaut

Publikováno v: Consciousness and Cognition. 19:341-351

This study focuses on Implicit learning (IL) in children. One of the main debates in this field concerns the occurrence of IL indicators in experimental settings and its manifestation in different populations. In this research, we are looking for evi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe7058fe2e21ab037d7bd3ea8cd7c417
https://doi.org/10.1016/j.concog.2009.09.006

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Clinical features of chromosome 22q11.2 microdeletion syndrome in 208 Chilean patients

Autor: Carmen Astete, Alonso Puga, Marcela Aracena, Juan F. Calderón, Gabriela M. Repetto, Arriaza M, Maria Luisa Guzman, Patricia Sanz, Teresa Aravena

Publikováno v: CLINICAL GENETICS
Artículos CONICYT
CONICYT Chile
instacron:CONICYT

Patients with chromosome 22q11 deletion syndrome exhibit significant phenotypic variability. Epidemiologic data suggest a higher incidence in Hispanics, but limited clinical information is available from Latin-American patients. We describe the clini

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d0ab5f8af43b00d5f251fe57d700a61
https://doi.org/10.1111/j.1399-0004.2009.01234.x

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